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| Product | Description | |
|---|---|---|
| 17α-hydroxyprogesterone deacetylase | A microsomal cytochrome P-450 (heme-thiolate) protein that catalyses two independent reactions at the same active site - the 17-hydroxylation of pregnenolone and progesterone, which is part of glucocorticoid hormones biosynthesis (EC 1.14.14.19), and the conversion of the 17-hydroxylated products via a 17,20-lyase reaction to form androstenedione and 3β-hydroxyandrost-5-en-17-one, leading to sex hormone biosynthesis. The activity of this reaction is dependent on the allosteric interaction of the enzyme with cytochrome b5 without any transfer of electrons from the cytochrome. The enzymes from different organisms differ in their substrate specificity. While the enzyme...son do not accept the former, and the enzyme from guinea pig does not accept the latter. Group: Enzymes. Synonyms: C-17/C-20 lyase; 17α-hydroxyprogesterone acetaldehyde-lyase; CYP17; CYP17A1 (gene name); 17α-hydroxyprogesterone 17,20-lyase. Enzyme Commission Number: EC 1.14.14.32. CAS No. 62213-24-5. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-0930; 17α-hydroxyprogesterone deacetylase; EC 1.14.14.32; 62213-24-5; C-17/C-20 lyase; 17α-hydroxyprogesterone acetaldehyde-lyase; CYP17; CYP17A1 (gene name); 17α-hydroxyprogesterone 17,20-lyase. Cat No: EXWM-0930. |  |
| 2'''-acetyl-6'''-hydroxyneomycin C deacetylase | Involved in the biosynthetic pathway of aminoglycoside antibiotics of the neomycin family. The enzyme from the bacterium Streptomyces fradiae also catalyses EC 3.5.1.112, 2'-N-acetylparomamine deacetylase. Group: Enzymes. Synonyms: neoL (gene name). Enzyme Commission Number: EC 3.5.1.113. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-4393; 2'''-acetyl-6'''-hydroxyneomycin C deacetylase; EC 3.5.1.113; neoL (gene name). Cat No: EXWM-4393. | |
| 2'-N-acetylparomamine deacetylase | Involved in the biosynthetic pathways of several clinically important aminocyclitol antibiotics, including kanamycin, butirosin, neomycin and ribostamycin. The enzyme from the bacterium Streptomyces fradiae can also accept 2'''-acetyl-6'''-hydroxyneomycin C as substrate, cf. EC 3.5.1.113, 2'''-acetyl-6'''-hydroxyneomycin C deacetylase. Group: Enzymes. Synonyms: btrD (gene name); neoL (gene name); kanN (gene name). Enzyme Commission Number: EC 3.5.1.112. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-4392; 2'-N-acetylparomamine deacetylase; EC 3.5.1.112; btrD (gene name); neoL (gene name); kanN (gene name). Cat No: EXWM-4392. | |
| 4-acetamidobutyrate deacetylase | Also acts on N-acetyl-β-alanine and 5-acetamidopentanoate. Group: Enzymes. Enzyme Commission Number: EC 3.5.1.63. CAS No. 102347-82-0. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-4453; 4-acetamidobutyrate deacetylase; EC 3.5.1.63; 102347-82-0. Cat No: EXWM-4453. | |
| 4-acetamidobutyryl-CoA deacetylase | The enzyme also hydrolyses 4-aminobutanoyl-CoA to aminobutanoate and coenzyme A. Group: Enzymes. Synonyms: aminobutyryl-CoA thiolesterase; deacetylase-thiolesterase. Enzyme Commission Number: EC 3.5.1.51. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-4440; 4-acetamidobutyryl-CoA deacetylase; EC 3.5.1.51; aminobutyryl-CoA thiolesterase; deacetylase-thiolesterase. Cat No: EXWM-4440. | |
| 5-(3,4-diacetoxybut-1-ynyl)-2,2'-bithiophene deacetylase | A highly specific enzyme from Tagetes patula. Group: Enzymes. Synonyms: diacetoxybutynylbithiophene acetate esterase; 3,4-diacetoxybutinylbithiophene:4-acetate esterase. Enzyme Commission Number: EC 3.1.1.66. CAS No. 95990-32-2. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-3494; 5-(3,4-diacetoxybut-1-ynyl)-2,2'-bithiophene deacetylase; EC 3.1.1.66; 95990-32-2; diacetoxybutynylbithiophene acetate esterase; 3,4-diacetoxybutinylbithiophene:4-acetate esterase. Cat No: EXWM-3494. | |
| 6-acetylglucose deacetylase | This enzyme belongs to the family of hydrolases, specifically those acting on carboxylic ester bonds. Group: Enzymes. Synonyms: 6-O-acetylglucose deacetylase. Enzyme Commission Number: EC 3.1.1.33. CAS No. 37278-46-9. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-3459; 6-acetylglucose deacetylase; EC 3.1.1.33; 37278-46-9; 6-O-acetylglucose deacetylase. Cat No: EXWM-3459. | |
| acetoxybutynylbithiophene deacetylase | The enzyme is highly specific. Group: Enzymes. Synonyms: acetoxybutynylbithiophene esterase; 5-(4-acetoxy-1-butynyl)-2,2'-bithiophene:acetate esterase. Enzyme Commission Number: EC 3.1.1.54. CAS No. 82346-63-2. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-3482; acetoxybutynylbithiophene deacetylase; EC 3.1.1.54; 82346-63-2; acetoxybutynylbithiophene esterase; 5-(4-acetoxy-1-butynyl)-2,2'-bithiophene:acetate esterase. Cat No: EXWM-3482. | |
| acetylornithine deacetylase | Also hydrolyses N-acetylmethionine. Group: Enzymes. Synonyms: acetylornithinase; N-acetylornithinase; 2-N-acetyl-L-ornithine amidohydrolase. Enzyme Commission Number: EC 3.5.1.16. CAS No. 9025-12-1. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-4405; acetylornithine deacetylase; EC 3.5.1.16; 9025-12-1; acetylornithinase; N-acetylornithinase; 2-N-acetyl-L-ornithine amidohydrolase. Cat No: EXWM-4405. | |
| acetylputrescine deacetylase | The enzyme from Micrococcus luteus also acts on N8-acetylspermidine and acetylcadaverine, but more slowly. Group: Enzymes. Enzyme Commission Number: EC 3.5.1.62. CAS No. 103679-48-7. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-4452; acetylputrescine deacetylase; EC 3.5.1.62; 103679-48-7. Cat No: EXWM-4452. | |
| acetylsalicylate deacetylase | Not identical with EC 3.1.1.1 (carboxylesterase), EC 3.1.1.2 (arylesterase), EC 3.1.1.7 (acetylcholinesterase) or EC 3.1.1.8 (cholinesterase). The activity of the liver cytosol enzyme is highest with acetyl esters of aryl alcohols, and thioesters are also hydrolysed; the microsomal enzyme also hydrolyses some other negatively charged esters, with highest activity on esters of salicylate with long-chain alcohols. Group: Enzymes. Synonyms: aspirin esterase; aspirin esterase; acetylsalicylic acid esterase; aspirin hydrolase. Enzyme Commission Number: EC 3.1.1.55. CAS No. 87348-04-7. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-3483; acetylsalicylate deacetylase; EC 3.1.1.55; 87348-04-7; aspirin esterase; aspirin esterase; acetylsalicylic acid esterase; aspirin hydrolase. Cat No: EXWM-3483. | |
| acetylspermidine deacetylase | It was initially thought that N1-acetylspermidine was the substrate for this deacetylase reaction but this has since been disproved by Marchant et al. Group: Enzymes. Synonyms: N8-monoacetylspermidine deacetylase; N8-acetylspermidine deacetylase; N-acetylspermidine deacetylase; N1-acetylspermidine amidohydrolase (incorrect); 8-N-acetylspermidine amidohydrolase. Enzyme Commission Number: EC 3.5.1.48. CAS No. 67339-07-5. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-4436; acetylspermidine deacetylase; EC 3.5.1.48; 67339-07-5; N8-monoacetylspermidine deacetylase; N8-acetylspermidine deacetylase; N-acetylspermidine deacetylase; N1-acetylspermidine amidohydrolase (incorrect); 8-N-acetylspermidine amidohydrolase. Cat No: EXWM-4436. | |
| Cancer Hydrolase KIAA1363 Inhibitor, JW480 (2-Isopropylphenyl-2- (2-naphthyl) ethylcarbamate, AADACL1 Inhibitor, Arylacetamide Deacetylase-Like 1 Inhibitor, NCEH1 Inhibitor, Neutral Cholesterol Ester Hydrolase 1 Inhibitor) | A membrane-permeable, highly potent and selective inhibitor against the 2-acetyl MAGE (monoakylglycerol ether) hydrolase KIAA1363/AADACL1 of both human (IC50=12nM; PC3 lysate) and murine (IC50=20nM; brain membrane samples) origin, with no significant effect toward other PC3 or murine brain serine hydrolase activities, including HSL, FAAH, and AChE. Readily crosses blood-brain barrier in mice and effectively suppresses PC3-derived tumor growth in mice in vivo (by 56% on day 33; 80mg/kg/day; o.g.). Also inhibits blood carboxylesterase. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 10mg. US Biological Life Sciences. |  Worldwide |
| cephalosporin-C deacetylase | Hydrolyses the acetyl ester bond on the 10-position of the antibiotic cephalosporin C. Group: Enzymes. Synonyms: cephalosporin C acetyl-hydrolase; cephalosporin C acetylase; cephalosporin acetylesterase; cephalosporin C acetylesterase; cephalosporin C acetyl-esterase; cephalosporin C deacetylase. Enzyme Commission Number: EC 3.1.1.41. CAS No. 52227-71-1. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-3468; cephalosporin-C deacetylase; EC 3.1.1.41; 52227-71-1; cephalosporin C acetyl-hydrolase; cephalosporin C acetylase; cephalosporin acetylesterase; cephalosporin C acetylesterase; cephalosporin C acetyl-esterase; cephalosporin C deacetylase. Cat No: EXWM-3468. | |
| Cephalosporin-C Deacetylase (Crude Enzyme) | This enzyme belongs to the family of hydrolases, specifically those acting on carboxylic ester bonds. This product with the indicated enzyme activity was briefly purified from engineered E. coli. Applications: Synthesis. Group: Enzymes. Synonyms: cephalosporin C acetyl-hydrolase; cephalosporin C acetylase; cephalosporin acetylesterase; cephalosporin C acetylesterase; cephalosporin C acetyl-esterase; cephalosporin C deacetylase. Enzyme Commission Number: EC 3.1.1.41. CAS No. 52227-71-1. Activity: Undetermined. Appearance: Clear to translucent yellow solution. Storage: at -20 °C or lower, for at least 1 month. Source: E. coli. cephalosporin C acetyl-hydrolase; cephalosporin C acetylase; cephalosporin acetylesterase; cephalosporin C acetylesterase; cephalosporin C acetyl-esterase; cephalosporin C deacetylase. Pack: 100ml. Cat No: NATE-1832. | |
| chitin deacetylase | Hydrolyses the N-acetamido groups of N-acetyl-D-glucosamine residues in chitin. Group: Enzymes. Enzyme Commission Number: EC 3.5.1.41. CAS No. 56379-60-3. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-4430; chitin deacetylase; EC 3.5.1.41; 56379-60-3. Cat No: EXWM-4430. | |
| chitin disaccharide deacetylase | Chitin oligosaccharide deacetylase is a key enzyme in the chitin catabolic cascade of chitinolytic Vibrio strains. Besides being a nutrient, the heterodisaccharide product 4-O-(N-acetyl-β-D-glucosaminyl)-D-glucosamine is a unique inducer of chitinase production in Vibrio parahemolyticus. In contrast to EC 3.5.1.41 (chitin deacetylase) this enzyme is specific for the chitin disaccharide. It also deacetylates the chitin trisaccharide with lower efficiency. No activity with higher polymers of GlcNAc. Group: Enzymes. Synonyms: chitobiose amidohydolase; COD; chitin oligosaccharide deacetylase; chitin oligosaccharide amidohydolase; 2-(acetylamino)-4-O-[2-(acetylamino)-2-deoxy-β-D-glucopyranosyl]-2-deoxy-D-glucopyranose acetylhydrolase. Enzyme Commission Number: EC 3.5.1.105. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-4384; chitin disaccharide deacetylase; EC 3.5.1.105; chitobiose amidohydolase; COD; chitin oligosaccharide deacetylase; chitin oligosaccharide amidohydolase; 2-(acetylamino)-4-O-[2-(acetylamino)-2-deoxy-β-D-glucopyranosyl]-2-deoxy-D-glucopyranose acetylhydrolase. Cat No: EXWM-4384. | |
| citrate-lyase deacetylase | In the proteobacterium Rubrivivax gelatinosus, this enzyme modulates the activity of EC 4.1.3.6, citrate (pro-3S)-lyase, by converting it from its active acetyl form into its inactive thiol form by removal of its acetyl groups. The activity of citrate-lyase deacetylase is itself inhibited by L-glutamate. Group: Enzymes. Synonyms: [citrate-(pro-3S)-lyase] thiolesterase; acetyl-S-(acyl-carrier protein) enzyme thioester hydrolase; citrate lyase deacetylase. Enzyme Commission Number: EC 3.1.2.16. CAS No. 58319-93-0. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-3550; citrate-lyase deacetylase; EC 3.1.2.16; 58319-93-0; [citrate-(pro-3S)-lyase] thiolesterase; acetyl-S-(acyl-carrier protein) enzyme thioester hydrolase; citrate lyase deacetylase. Cat No: EXWM-3550. | |
| Diacetylchitobiose deacetylase from Bacillus cereus, Recombinant | Diacetylchitobiose deacetylase is an enzyme from Bacillus cereus that exhibits deacetylase activity to the N-acetyl moiety of the N-acetylglucosamine and the diacetylchitobiose and triacetylchitotriose. Group: Enzymes. Synonyms: N,N'-diacetylchitobiose deacetylase (nonreducing end); EC 3.5.1.-. Enzyme Commission Number: EC 3.5.1.-. Purity: >90% as judged by SDS-PAGE. Diacetylchitobiose deacetylase. Mole weight: 28.3 kDa. Storage: This enzyme is shipped at room temperature but should be stored at -20 °C. Form: 35 mM NaHepes buffer, pH 7.5, 750 mM NaCl, 200 mM imidazol, 3.5 mM CaCl2, 0.02% sodium azide and 25% (v/v) glycerol. Source: E. coli. Species: Bacillus cereus. N,N'-diacetylchitobiose deacetylase (nonreducing end); EC 3.5.1.-. Cat No: NATE-1542. | |
| HDAC Inhibitor XVII ((E)-N-Hydroxy-4-methoxy-2-(biphenyl-4-yl)cinnamide, Histone Deacetylase Inhibitor XVII) | A cell-permeable N-hydroxycinnamide derivative that acts a highly potent and HDAC8-selective histone deacetylase inhibitor (IC50 = 27nM), displaying much reduced or little potency against HDAC1/3 (IC50 = 3.0uM), HDAC2/4/6/10/11 (IC50 >20uM), or total HDAC activity in HeLa nuclear extract (IC50 >10uM). Reported to preferentially inhibit the proliferation of human lung cancer cells CL1-5, H1299, and A549 (IC50 from 7 to 8uM), while being much less toxic to normal human lung IMR-90 cells (73% inhibition at 40uM). Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 10mg. Molecular Formula: C??H??NO?, Primary Target IC50: 27nM. US Biological Life Sciences. | Worldwide |
| histone deacetylase | A class of enzymes that remove acetyl groups from N6-acetyl-lysine residues on a histone. The reaction of this enzyme is opposite to that of EC 2.3.1.48, histone acetyltransferase. Histone deacetylases (HDACs) can be organized into three classes, HDAC1, HDAC2 and HDAC3, depending on sequence similarity and domain organization. Histone acetylation plays an important role in regulation of gene expression. In eukaryotes, HDACs play a key role in the regulation of transcription and cell proliferation. May be identical to EC 3.5.1.17, acyl-lysine deacylase. Group: Enzymes. Synonyms: HDAC. Enzyme Commission Number: EC 3.5.1.98. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-4490; histone deacetylase; EC 3.5.1.98; HDAC. Cat No: EXWM-4490. | |
| methylumbelliferyl-acetate deacetylase | Acts on short-chain acyl esters of 4-methylumbelliferone, but not on naphthyl, indoxyl or thiocholine esters. Group: Enzymes. Synonyms: esterase D. Enzyme Commission Number: EC 3.1.1.56. CAS No. 83380-83-0. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-3484; methylumbelliferyl-acetate deacetylase; EC 3.1.1.56; 83380-83-0; esterase D. Cat No: EXWM-3484. | |
| N-acetyl-1-D-myo-inositol-2-amino-2-deoxy-α-D-glucopyranoside deacetylase | This enzyme is considered the key enzyme and rate limiting step in the mycothiol biosynthesis pathway. In addition to acetylase activity, the enzyme possesses weak activity of EC 3.5.1.115, mycothiol S-conjugate amidase, and shares sequence similarity with that enzyme. The enzyme requires a divalent transition metal ion for activity, believed to be Zn2+. Group: Enzymes. Synonyms: MshB. Enzyme Commission Number: EC 3.5.1.103. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-4382; N-acetyl-1-D-myo-inositol-2-amino-2-deoxy-α-D-glucopyranoside deacetylase; EC 3.5.1.103; MshB. Cat No: EXWM-4382. | |
| N-acetyl-β-alanine deacetylase | This enzyme belongs to the family of hydrolases, those acting on carbon-nitrogen bonds other than peptide bonds, specifically in linear amides. This enzyme participates in beta-alanine metabolism. Group: Enzymes. Enzyme Commission Number: EC 3.5.1.21. CAS No. 37289-04-6. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-4411; N-acetyl-β-alanine deacetylase; EC 3.5.1.21; 37289-04-6. Cat No: EXWM-4411. | |
| N-acetyldiaminopimelate deacetylase | This enzyme belongs to the family of hydrolases, those acting on carbon-nitrogen bonds other than peptide bonds, specifically in linear amides. The systematic name of this enzyme class is N6-acetyl-LL-2,6-diaminoheptanedioate amidohydrolase. Other names in common use include N-acetyl-L-diaminopimelic acid deacylase, N-acetyl-LL-diaminopimelate deacylase, and 6-N-acetyl-LL-2,6-diaminoheptanedioate amidohydrolase. This enzyme participates in lysine biosynthesis. Group: Enzymes. Synonyms: N-acetyl-L-diaminopimelic acid deacylase; N-acetyl-LL-diaminopimelate deacylase; 6-N-acetyl-LL-2,6-diaminoheptanedioate amidohydrolase. Enzyme Commission Number: EC 3.5.1.47. CAS No. 99193-93-8. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-4435; N-acetyldiaminopimelate deacetylase; EC 3.5.1.47; 99193-93-8; N-acetyl-L-diaminopimelic acid deacylase; N-acetyl-LL-diaminopimelate deacylase; 6-N-acetyl-LL-2,6-diaminoheptanedioate amidohydrolase. Cat No: EXWM-4435. | |
| N-acetylgalactosaminoglycan deacetylase | This enzyme belongs to the family of hydrolases, specifically those acting on carboxylic ester bonds. Group: Enzymes. Synonyms: polysaccharide deacetylase (misleading); Vi-polysaccharide deacetylase; N-acetyl galactosaminoglycan deacetylase. Enzyme Commission Number: EC 3.1.1.58. CAS No. 52410-59-0. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-3486; N-acetylgalactosaminoglycan deacetylase; EC 3.1.1.58; 52410-59-0; polysaccharide deacetylase (misleading); Vi-polysaccharide deacetylase; N-acetyl galactosaminoglycan deacetylase. Cat No: EXWM-3486. | |
| N-acetylglucosamine-6-phosphate deacetylase | This enzyme belongs to the family of hydrolases, those acting on carbon-nitrogen bonds other than peptide bonds, specifically in linear amides. The systematic name of this enzyme class is N-acetyl-D-glucosamine-6-phosphate amidohydrolase. Other names in common use include acetylglucosamine phosphate deacetylase, acetylaminodeoxyglucosephosphate acetylhydrolase, and 2-acetamido-2-deoxy-D-glucose-6-phosphate amidohydrolase. This enzyme participates in aminosugars metabolism. Group: Enzymes. Synonyms: acetylglucosamine phosphate deacetylase; acetylaminodeoxyglucosephosphate acetylhydrolase; 2-acetamido-2-deoxy-D-glucose-6-phosphate amidohydrolase. Enzyme Commission Number: EC 3.5.1.25. CAS No. 9027-50-3. N-acetylglucosamine 6-phosphate deacetylase. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-4415; N-acetylglucosamine-6-phosphate deacetylase; EC 3.5.1.25; 9027-50-3; acetylglucosamine phosphate deacetylase; acetylaminodeoxyglucosephosphate acetylhydrolase; 2-acetamido-2-deoxy-D-glucose-6-phosphate amidohydrolase. Cat No: EXWM-4415. | |
| N-acetylglucosamine 6-phosphate deacetylase from Bacillus subtilis, Recombinant | In enzymology, a N-acetylglucosamine-6-phosphate deacetylase (EC 3.5.1.25) is an enzyme that catalyzes the chemical reaction: N-acetyl-D-glucosamine 6-phosphate + H2O ? D-glucosamine 6-phosphate + acetate. Thus, the two substrates of this enzyme are N-acetyl-D-glucosamine 6-phosphate and H2O, whereas its two products are D-glucosamine 6-phosphate and acetate. Group: Enzymes. Synonyms: N-acetyl-D-glucosamine-6-phosphate amidohydrolase; acetylglucosamine phosphate deacetylase; acetylaminodeoxyglucosephosphate acetylhydrolase; 2-acetamido-2-deoxy-D-glucose-6-phosphate amidohydrolase; EC 3.5.1.25. Enzyme Commission Number: EC 3.5.1.25. CAS No. 9027-50-3. Purity: >90% as judged by SDS-PAGE. N-acetylglucosamine 6-phosphate deacetylase. Mole weight: 44.6 kDa. Storage: This enzyme is shipped at room temperature but should be stored at -20 °C. Form: 35 mM NaHepes buffer, pH 7.5, 750 mM NaCl, 200 mM imidazol, 3.5 mM CaCl2, 0.02% sodium azide and 25% (v/v) glycerol. Source: E. coli. Species: Bacillus subtilis. N-acetyl-D-glucosamine-6-phosphate amidohydrolase; acetylglucosamine phosphate deacetylase; acetylaminodeoxyglucosephosphate acetylhydrolase; 2-acetamido-2-deoxy-D-glucose-6-phosphate amidohydrolase; EC 3.5.1.25. Cat No: NATE-1541. | |
| N-acetylglucosamine 6-phosphate deacetylase from Escherichia coli, Recombinant | In enzymology, a N-acetylglucosamine-6-phosphate deacetylase (EC 3.5.1.25) is an enzyme that catalyzes the chemical reaction: N-acetyl-D-glucosamine 6-phosphate + H2O ? D-glucosamine 6-phosphate + acetate. Thus, the two substrates of this enzyme are N-acetyl-D-glucosamine 6-phosphate and H2O, whereas its two products are D-glucosamine 6-phosphate and acetate. Group: Enzymes. Synonyms: N-acetyl-D-glucosamine-6-phosphate amidohydrolase; acetylglucosamine phosphate deacetylase; acetylaminodeoxyglucosephosphate acetylhydrolase; 2-acetamido-2-deoxy-D-glucose-6-phosphate amidohydrolase; EC 3.5.1.25. Enzyme Commission Number: EC 3.5.1.25. CAS No. 9027-50-3. Purity: >90% as judged by SDS-PAGE. N-acetylglucosamine 6-phosphate deacetylase. Mole weight: 43.0 kDa. Storage: This enzyme is shipped at room temperature but should be stored at -20 °C. Form: 35 mM NaHepes buffer, pH 7.5, 750 mM NaCl, 200 mM imidazol, 3.5 mM CaCl2, 0.02% sodium azide and 25% (v/v) glycerol. Source: E. coli. Species: Escherichia coli. N-acetyl-D-glucosamine-6-phosphate amidohydrolase; acetylglucosamine phosphate deacetylase; acetylaminodeoxyglucosephosphate acetylhydrolase; 2-acetamido-2-deoxy-D-glucose-6-phosphate amidohydrolase; EC 3.5.1.25. Cat No: NATE-1540. | |
| N-acetylglucosamine deacetylase | This enzyme belongs to the family of hydrolases, those acting on carbon-nitrogen bonds other than peptide bonds, specifically in linear amides. The systematic name of this enzyme class is N-acetyl-D-glucosamine amidohydrolase. Other names in common use include acetylaminodeoxyglucose acetylhydrolase, and N-acetyl-D-glucosaminyl N-deacetylase. This enzyme participates in aminosugars metabolism. Group: Enzymes. Synonyms: acetylaminodeoxyglucose acetylhydrolase; N-acetyl-D-glucosaminyl N-deacetylase. Enzyme Commission Number: EC 3.5.1.33. CAS No. 9012-32-2. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-4423; N-acetylglucosamine deacetylase; EC 3.5.1.33; 9012-32-2; acetylaminodeoxyglucose acetylhydrolase; N-acetyl-D-glucosaminyl N-deacetylase. Cat No: EXWM-4423. | |
| N-acetyl glucosaminyl phosphatidyl inositol deacetylase | Involved in the second step of glycosylphosphatidylinositol (GPI) anchor formation in all eukaryotes. The enzyme appears to be composed of a single subunit (PIG-L in mammalian cells and GPI12 in yeast). In some species, the long-chain sn-1-acyl group of the phosphatidyl group is replaced by a long-chain alkyl or alk-1-enyl group. Group: Enzymes. Synonyms: N-acetyl-D-glucosaminylphosphatidylinositol acetylhydrolase; N-acetyl glucosaminyl phosphatidyl inositol de-N-acetylase; GlcNAc-PI de-N-acetylase; GlcNAc-PI deacetylase; acetyl glucosaminyl phosphatidyl inositol deacetylase. Enzyme Commission Number: EC 3.5.1.89. CAS No. 122191-30-4. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-4480; N-acetyl glucosaminyl phosphatidyl inositol deacetylase; EC 3.5.1.89; 122191-30-4; N-acetyl-D-glucosaminylphosphatidylinositol acetylhydrolase; N-acetyl glucosaminyl phosphatidyl inositol de-N-acetylase; GlcNAc-PI de-N-acetylase; GlcNAc-PI deacetylase; acetyl glucosaminyl phosphatidyl inositol deacetylase. Cat No: EXWM-4480. | |
| NAD-dependent protein deacetylase sirtuin-2 (192-200) | NAD-dependent protein deacetylase sirtuin-2 (192-200) is amino acids 192 to 200 fragment of NAD-dependent protein deacetylase sirtuin-2. NAD-dependent protein deacetylase sirtuin-2 plays a major role in the control of cell cycle progression and genomic stability. Synonyms: Regulatory protein SIR2 homolog 2 (192-200); SIR2-like protein 2 (192-200). |  |
| peptidoglycan-N-acetylglucosamine deacetylase | Modification of peptidoglycan by N-deacetylation is an important factor in virulence of Helicobacter pylori,Listeria monocytogenes and Streptococcus suis. The enzyme from Streptococcus pneumoniae is a metalloenzyme using a His-His-Asp zinc-binding triad with a nearby aspartic acid and histidine acting as the catalytic base and acid, respectively. Group: Enzymes. Synonyms: HP310; PgdA; SpPgdA; BC1960; peptidoglycan deacetylase; N-acetylglucosamine deacetylase; peptidoglycan GlcNAc deacetylase; peptidoglycan N-acetylglucosamine deacetylase; PG N-deacetylase. Enzyme Commission Number: EC 3.5.1.104. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-4383; peptidoglycan-N-acetylglucosamine deacetylase; EC 3.5.1.104; HP310; PgdA; SpPgdA; BC1960; peptidoglycan deacetylase; N-acetylglucosamine deacetylase; peptidoglycan GlcNAc deacetylase; peptidoglycan N-acetylglucosamine deacetylase; PG N-deacetylase. Cat No: EXWM-4383. | |
| Peptidoglycan N-acetylglucosamine deacetylase from Streptococcus pneumoniae, Recombinant | Peptidoglycan-N-acetylglucosamine deacetylase (EC 3.5.1.104, HP310, PgdA, SpPgdA, BC1960, peptidoglycan deacetylase, N-acetylglucosamine deacetylase, peptidoglycan GlcNAc deacetylase, peptidoglycan N-acetylglucosamine deacetylase, PG N-deacetylase) is an enzyme with systematic name peptidoglycan-N-acetylglucosamine amidohydrolase. This enzyme catalyses the following chemical reaction: peptidoglycan-N-acetyl-D-glucosamine + H2O ? peptidoglycan-D-glucosamine + acetate. This enzyme contributes to virulence of Helicobacter pylori, Listeria monocytogenes and Streptococcus suis. Group: Enzymes. Synonyms: Peptidoglycan-N-acetylglucosamine de. Enzyme Commission Number: EC 3.5.1.-. Purity: >90% as judged by SDS-PAGE. Peptidoglycan N-acetylglucosamine deacetylase. Mole weight: 24.2 kDa. Storage: This enzyme is shipped at room temperature but should be stored at -20 °C. Form: 35 mM NaHepes buffer, pH 7.5, 750 mM NaCl, 200 mM imidazol, 3.5 mM CaCl2, 0.02% sodium azide and 25% (v/v) glycerol. Source: E. coli. Species: Streptococcus pneumoniae. Peptidoglycan-N-acetylglucosamine deacetylase; EC 3.5.1.-; HP310; PgdA; SpPgdA; BC1960; peptidoglycan deacetylase; N-acetylglucosamine deacetylase; peptidoglycan GlcNAc deacetylase; peptidoglycan N-acetylglucosamine deacetylase; PG N-deacetylase. Cat No: NATE-1539. | |
| Sodium Butyrate, 0.5M (Histone Deacetylase Inhibitor) | A short chain fatty acid shown to be an inhibitor of histone deacetylase (HDAC). Induce apoptosis in colon carcinoma cell lines in a p53-independent pathway. Inhibits c-myc splicing and inteferes with signal transduction processes, including the release of Ca2+ from intracellular stores. Downregulates the activity of serine/threonine protease kinase casein kinase II in HT29 cells. Group: Biochemicals. Grades: Highly Purified. CAS No. 156-54-7. Pack Sizes: 10ml, 25ml, 50ml. Molecular Formula: C?H?NaO?, Molecular Weight: 110.09. US Biological Life Sciences. | Worldwide |
| Sodium Butyrate, 1M (Histone Deacetylase Inhibitor) | A short chain fatty acid shown to be an inhibitor of histone deacetylase (HDAC). Induce apoptosis in colon carcinoma cell lines in a p53-independent pathway. Inhibits c-myc splicing and inteferes with signal transduction processes, including the release of Ca2+ from intracellular stores. Downregulates the activity of serine/threonine protease kinase casein kinase II in HT29 cells. Group: Biochemicals. Grades: Highly Purified. CAS No. 156-54-7. Pack Sizes: 10ml, 25ml, 50ml. Molecular Formula: C?H?NaO?, Molecular Weight: 110.09. US Biological Life Sciences. | Worldwide |
| Trichostatin A (TSA) (Histone Deacetylase Inhibitor)89/1/20 | Trichostatin A is an antifungal antibiotic that is a reversible, potent and specific inhibitor of mammalian histone deacetylase (HDAC) both in vivo and in vitro. Histone deacetylase inhibition causes chromatin relaxation and gene expression modulation. May induce apoptosis. TSA inhibits the eukaryotic cell cycle and induces morphological reversion of transformed cells. It blocks cell cycle progression at G1 phase in Hela Cells. TSA causes accumulation of highly acetylated histones in vivo, while inhibiting the activity of partially purified histone deacetylase in vitro. Group: Biochemicals. Alternative Names: 4,6-Dimethyl-7-[p-dimethylaminophenyl]- 7-oxohepta-2, 4-dienohydroxamic acid). Grades: Highly Purified. CAS No. 58880-19-6. Pack Sizes: 1mg, 5mg. US Biological Life Sciences. | Worldwide |
| UDP-3-O-acyl-N-acetylglucosamine deacetylase | A zinc protein. The enzyme catalyses a committed step in the biosynthesis of lipid A. Group: Enzymes. Synonyms: LpxC protein; LpxC enzyme; LpxC deacetylase; deacetylase LpxC; UDP-3-O-acyl-GlcNAc deacetylase; UDP-3-O-((R)-3-hydroxymyristoyl)-N-acetylglucosamine deacetylase; UDP-(3-O-acyl)-N-acetylglucosamine deacetylase; UDP-3-O-(R-3-hydroxymyristoyl)-N-acetylglucosamine deacetylase; UDP-(3-O-(R-3-hydroxymyristoyl))-N-acetylglucosamine deacetylase; UDP-3-O-[(3R)-3-hydroxymyristoyl]-N-acetylglucosamine amidohydrolase. Enzyme Commission Number: EC 3.5.1.108. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-4387; UDP-3-O-acyl-N-acetylglucosamine deacetylase; EC 3.5.1.108; LpxC protein; LpxC enzyme; LpxC deacetylase; deacetylase LpxC; UDP-3-O-acyl-GlcNAc deacetylase; UDP-3-O-((R)-3-hydroxymyristoyl)-N-acetylglucosamine deacetylase; UDP-(3-O-acyl)-N-acetylglucosamine deacetylase; UDP-3-O-(R-3-hydroxymyristoyl)-N-acetylglucosamine deacetylase; UDP-(3-O-(R-3-hydroxymyristoyl))-N-acetylglucosamine deacetylase; UDP-3-O-[(3R)-3-hydroxymyristoyl]-N-acetylglucosamine amidohydrolase. Cat No: EXWM-4387. | |
| UDP-acetylglucosamine deacetylase from Escherichia coli, Recombinant | UDP-acetylglucosamine deacetylase is a metal-dependent deacetylase from Escherichia coli that removes the acetyl group from the 2-amino group of UDP-(3-O-(R-3-hydroxymyristoyl))-N-acetylglucosamine (myr-UDP-GlcNAc)3. Group: Enzymes. Synonyms: EC 3.5.1.-; metal-dependent deacetylase; UDP-acetylglucosamine deacetylase. Enzyme Commission Number: EC 3.5.1.-. Purity: >90% as judged by SDS-PAGE. UDP-acetylglucosamine deacetylase. Mole weight: 36.0 kDa. Storage: This enzyme is shipped at room temperature but should be stored at -20 °C. Form: 35 mM NaHepes buffer, pH 7.5, 750 mM NaCl, 200 mM imidazol, 3.5 mM CaCl2, 0.02% sodium azide and 25% (v/v) glycerol. Source: E. coli. Species: Escherichia coli. EC 3.5.1.-; metal-dependent deacetylase; UDP-acetylglucosamine deacetylase. Cat No: NATE-1537. | |
| UDP-acetylglucosamine deacetylase from Pseudomonas aeruginosa, Recombinant | UDP-acetylglucosamine deacetylase is a metal-dependent deacetylase from Escherichia coli that removes the acetyl group from the 2-amino group of UDP-(3-O-(R-3-hydroxymyristoyl))-N-acetylglucosamine (myr-UDP-GlcNAc)3. Group: Enzymes. Synonyms: EC 3.5.1.-; metal-dependent deacetylase; UDP-acetylglucosamine deacetylase. Enzyme Commission Number: EC 3.5.1.-. Purity: >90% as judged by SDS-PAGE. UDP-acetylglucosamine deacetylase. Mole weight: 35.5 kDa. Storage: This enzyme is shipped at room temperature but should be stored at -20 °C. Form: 35 mM NaHepes buffer, pH 7.5, 750 mM NaCl, 200 mM imidazol, 3.5 mM CaCl2, 0.02% sodium azide and 25% (v/v) glycerol. Source: E. coli. Species: Pseudomonas aeruginosa. EC 3.5.1.-; metal-dependent deacetylase; UDP-acetylglucosamine deacetylase. Cat No: NATE-1538. | |
| 1-(2,4-Dichlorobenzoyl)-1H-benzotriazole | Histone deacetylase (HDAC) inhibitors are able to interrupt cell cycle progression in transformed cell lines and may be explored as new clinical agents in cancer therapy. 1-(2,4-Dichlorobenzoyl)-1H-benzotriazole has been shown to suppress the biological effects induced by the HDAC inhibitor, Trichostatin A (T774710). Group: Biochemicals. Grades: Highly Purified. CAS No. 200626-61-5. Pack Sizes: 10mg, 25mg. Molecular Formula: C13H7Cl2N3O, Molecular Weight: 292.12. US Biological Life Sciences. | Worldwide |
| 1-(2-Aminothiazol-4-yl)ethanone | 1-(2-Aminothiazol-4-yl)ethanone is a versatile reactant, used as intermediate in preparation of multicyclic sulfonamide compounds as histone deacetylase inhibitors useful in treatment and prevention of diseases. Group: Biochemicals. Grades: Highly Purified. CAS No. 101258-16-6. Pack Sizes: 25mg, 50mg. Molecular Formula: C5H6N2OS, Molecular Weight: 142.18. US Biological Life Sciences. | Worldwide |
| 1- (4- (1, 3, 4-Oxadiazol-2-yl) phenyl) -3- ( (5- (2, 2, 2-trifluoroacetyl) thiophene-2-carbonyl) oxy) guanidine | 1- (4- (1, 3, 4-Oxadiazol-2-yl) phenyl) -3- ( (5- (2, 2, 2-trifluoroacetyl) thiophene-2-carbonyl) oxy) guanidine is an intermediate in the synthesis of potential class II human histone deacetylase inhibitors. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 2.5mg, 10mg. Molecular Formula: C16H10F3N5O4S. US Biological Life Sciences. | Worldwide |
| 1-(4-Hydroxyphenyl)-2-chloroethanol | 1-(4-Hydroxyphenyl)-2-chloroethanol is synthesized from 2-Chloro-1-(4-hydroxy-phenyl)-ethanone. 2-Chloro-1-(4-hydroxy-phenyl)-ethanone is a reagent that is used in the preparation of hydroxypyrimidine derivatives and their HDAC (histone deacetylases) inhibitory activity. Group: Biochemicals. Grades: Highly Purified. CAS No. 4973-17-5. Pack Sizes: 250mg, 2.5g. Molecular Formula: C8H9ClO2, Molecular Weight: 172.61. US Biological Life Sciences. | Worldwide |
| 1-Alaninechlamydocin | It is a cyclic tetrapeptide antibiotic containing a single β-amino acid, which was isolated from diheterospora chlamydosporia in 1992. It is less widely characterised than the related chlamydocin. It exhibits potent antitumor activity and acts by inhibiting histone deacetylase. Synonyms: Cyclo[L-alanyl-L-phenylalanyl-D-prolyl-(αS,2S)-α-amino-η-oxooxiraneoctanoyl]; (S)-Cyclo(L-alanyl-L-phenylalanyl-D-prolyl-η-oxo-L-α-aminooxiraneoctanoyl). Grades: >95% by HPLC. CAS No. 141446-96-0. Molecular formula: C27H36N4O6. Mole weight: 512.61. | |
| 1-?Aminocycloheptane car?boxylic Acid | 1-?Aminocycloheptane car?boxylic Acid is used in the synthesis of chlamydocin-hydroxamic acid analogs with histone deacetylase inhibitory activities. It is also used to prepare imidazobioxazolium triflates as precursors for sterically hindered and electron-donating N-heterocyclic carbene ligands. Group: Biochemicals. Grades: Highly Purified. CAS No. 6949-77-5. Pack Sizes: 250mg, 1g. Molecular Formula: C8H15NO2, Molecular Weight: 157.21. US Biological Life Sciences. | Worldwide |
| 1-Methyl-1,8-diazaspiro[4.5]decane Dihydrochloride | 1-Methyl-1,8-diazaspiro[4.5]decane Dihydrochloride is used in the image-guided synthesis of potent blood-brain barrier permeable histone deacetylase inhibitors. Group: Biochemicals. Grades: Highly Purified. CAS No. 1432679-85-0. Pack Sizes: 10mg, 25mg. Molecular Formula: C9H18N2; HCi, Molecular Weight: 154.252364599999. US Biological Life Sciences. | Worldwide |
| 1-(Pyrazin-2-yl)-2-trifluoroacetyl Hydrazine | 1-(Pyrazin-2-yl)-2-trifluoroacetyl Hydrazine can be used as reactant/reagent in synthetic preparation of tricyclic hydroxamic acids as inhibitors of histone deacetylase. Group: Biochemicals. Grades: Highly Purified. CAS No. 837430-15-6. Pack Sizes: 2.5mg, 5mg. Molecular Formula: C6H5F3N4O, Molecular Weight: 206.13. US Biological Life Sciences. | Worldwide |
| 2-?[[2-? (Dimethylamino) ?ethyl]?thio]?-acetic Acid | 2-?[[2-? (Dimethylamino) ?ethyl]?thio]?-acetic Acid functions as a co-drugs, and also acts as a reagent for the preparation of hydroxamate-based histone deacetylase inhibitors for enhancing activity of antifungal agents which inhibit a step in the ergosterol synthesis pathway. Group: Biochemicals. Grades: Highly Purified. CAS No. 933682-63-4. Pack Sizes: 1g, 10g. Molecular Formula: C6H13NO2S, Molecular Weight: 163.24. US Biological Life Sciences. | Worldwide |
| 2-[4- (1, 3, 4-Oxadiazol-2-yl) phenoxy]acetamidoxime | 2-[4- (1, 3, 4-Oxadiazole-2-yl) phenoxy]acetamidoxime is a reagent that is used to synthesize fluoroacetylthiophene oxadiazoles as class II human histone deacetylase inhibitors. Group: Biochemicals. Grades: Highly Purified. CAS No. 258521-20-9. Pack Sizes: 100mg, 1g. Molecular Formula: C10H10N4O3. US Biological Life Sciences. | Worldwide |
| 2-[4- (1, 3, 4-Oxadiazol-2-yl) phenoxy]acetonitrile | 2-[4- (1, 3, 4-Oxadiazol-2-yl) phenoxy]acetonitrile is an intermediate in the synthesis of potential class II human histone deacetylase inhibitors. Group: Biochemicals. Grades: Highly Purified. CAS No. 871218-36-9. Pack Sizes: 100mg, 250mg. Molecular Formula: C10H7N3O2. US Biological Life Sciences. | Worldwide |
| 2,4,6-Tribromobenzyl Bromide | 2,4,6-Tribromobenzyl Bromide acts as a reagent for the design, synthesis and biological evaluation of novel histone deacetylase 1 inhibitors through click chemistry. Group: Biochemicals. Grades: Highly Purified. CAS No. 54459-64-2. Pack Sizes: 10g, 25g. Molecular Formula: C7H4Br4, Molecular Weight: 407.72. US Biological Life Sciences. | Worldwide |
| [2-(4-Fluorophenyl)thiazol-4-yl]methanol | [2-(4-Fluorophenyl)thiazol-4-yl]methanol is an intermediate used in preparation of azole compounds as histone deacetylase (HDAC) inhibitors. Group: Biochemicals. Grades: Highly Purified. CAS No. 885280-13-7. Pack Sizes: 100mg, 250mg. Molecular Formula: C10H8FNOS, Molecular Weight: 209.24. US Biological Life Sciences. | Worldwide |
| 2- [ (4-Nitrophenyl) methylene] hydrazinecarboxamide | 2- [ (4-Nitrophenyl) methylene] hydrazinecarboxamide can be used to prepare benzimidazole derivatives. It is also a useful compound for developing histone deacetylase inhibitors. Group: Biochemicals. Grades: Highly Purified. CAS No. 5315-87-7. Pack Sizes: 100mg, 250mg. Molecular Formula: C8H8N4O3, Molecular Weight: 208.17. US Biological Life Sciences. | Worldwide |
| 2-Acetamido-2-deoxy-b-D-glucopyranosyl serine | 2-Acetamido-2-deoxy-b-D-glucopyranosyl serine, an essential compound in the biomedical sector, plays a crucial role in the production of different glycopeptide antibiotics. Moreover, it also demonstrates its therapeutic potentialities by suppressing the activity of N-deacetylases in cells, which could be applicable in various diseases such as cancer. Given the multifaceted implications of this compound, it remains a topic of interest in the scientific community. | |
| 2-?Amino-?N-?(1-?phenyl-?ethyl)?-?benzamide | 2-?Amino-?N-?(1-?phenyl-?ethyl)?-?benzamide is a reagent used in the synthesis of potent inhibitors of class III histone/protein deacetylases. As well, used to prepare agents promoting anticonvulsant activity. Group: Biochemicals. Grades: Highly Purified. CAS No. 85592-80-9. Pack Sizes: 250mg, 500mg. Molecular Formula: C15H16N2O. US Biological Life Sciences. | Worldwide |
| 2-Chloro-1-(4-hydroxy-phenyl)-ethanone | 2-Chloro-1-(4-hydroxy-phenyl)-ethanone is a reagent that is used in the preparation of hydroxypyrimidine derivatives and their HDAC (histone deacetylases) inhibitory activity. Group: Biochemicals. Grades: Highly Purified. CAS No. 6305-04-0. Pack Sizes: 500mg, 5g. Molecular Formula: C8H7ClO2, Molecular Weight: 170.59. US Biological Life Sciences. | Worldwide |
| 2-Ethynylbiphenyl-13C6 | 2-Ethynylbiphenyl-13C6 is a reactant used in the preparation of labelled histone deacetylase (HDAC) inhibitors and EGFR tyrosine inhibitors. Group: Biochemicals. Alternative Names: 1-Ethynyl-2-phenylbenzene13C6; 2-Biphenylylacetylene 13C6. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| 2-Formylcyclopropane-1-carboxylic Acid Ethyl Ester | 2-Formylcyclopropane-1-carboxylic Acid Ethyl Ester acts as a reagent for the design, synthesis and biological evaluation of first-in-class dual acting histone deacetylase (HDACs) and phosphodiesterase 5 (PDE5) inhibitors for treatment of Alzheimers disease. Group: Biochemicals. Grades: Highly Purified. CAS No. 20417-61-2. Pack Sizes: 250mg, 500mg. Molecular Formula: C7H10O3, Molecular Weight: 142.15. US Biological Life Sciences. | Worldwide |
| 2-Hexyl-4-pentynoic acid | 2-hexyl-4-pentynoic acid is a derivative of valproic acid, an inhibitor of histone deacetylases (HDACs). It inhibits HDAC activity more potently (IC50 = 13 μM) than valproic acid (IC50 = 398 μM). Synonyms: 2-(prop-2-yn-1-yl)octanoic acid. Grades: ≥95%. CAS No. 96017-59-3. Molecular formula: C11H18O2. Mole weight: 182.3. | |
| 2-Methyl-5-nitrobenzenesulfonamide | 2-Methyl-5-nitrobenzenesulfonamide (CAS# 6269-91-6) is a chemical reagent in the synthesis of good inhibitors of cancer-related carbonic anhydrase. Also used in the synthesis of novel deacetylase inhibitors used in anti-tumor therapy. Synonyms: 2-methyl-5-nitrobenzenesulfonamide; 2-methyl-5-nitrobenzenesulfonamide. Grades: 98 %. CAS No. 6269-91-6. Molecular formula: C7H8N2O4S. Mole weight: 216.21. | |
| 2-Methyl-5-nitro Benzene sulfonamide | 2-Methyl-5-nitro Benzene sulfonamide is a chemical reagent in the synthesis of good inhibitors of cancer-related carbonic anhydrase. Also used in the synthesis of novel deacetylase inhibitors used in anti-tumor therapy. Group: Biochemicals. Grades: Highly Purified. CAS No. 6269-91-6. Pack Sizes: 1g, 5g. Molecular Formula: C7H8N2O4S, Molecular Weight: 216.21. US Biological Life Sciences. | Worldwide |
| 2-?Nitrophenyl Isocyanate | 2-?Nitrophenyl Isocyanate is a reagent used in the synthesis of histone deacetylase class III inhibitors which exhibit antiproliferative activity against cancer cell lines. Group: Biochemicals. Grades: Highly Purified. CAS No. 3320-86-3. Pack Sizes: 250mg, 1g. Molecular Formula: C7H4N2O3, Molecular Weight: 164.12. US Biological Life Sciences. | Worldwide |
| 2-Oxo-1,2,3,4-tetrahydroquinoline-6-sulfonyl Chloride | 2-Oxo-1,2,3,4-tetrahydroquinoline-6-sulfonyl Chloride is a reactant used in the synthesis of pan-histone deacetylase (pan-HDAC) inhibitors. Group: Biochemicals. Grades: Highly Purified. CAS No. 66657-42-9. Pack Sizes: 100mg, 250mg. Molecular Formula: C9H8ClNO3S, Molecular Weight: 245.68. US Biological Life Sciences. | Worldwide |
| (2-Thienylthio) acetonitrile | (2-Thienylthio) acetonitrile is an intermediate in the synthesis of possible class II human histone deacetylase inhibitor. Group: Biochemicals. Grades: Highly Purified. CAS No. 26031-45-8. Pack Sizes: 1g, 5g. Molecular Formula: C6H5NS2. US Biological Life Sciences. | Worldwide |
| 3-[ (2-Thienylsulfonyl) methyl]-5-[5-trifluoroacetyl-thien-2-yl]-1, 2, 4-oxadiazole | 3-[ (2-Thienylsulfonyl) methyl]-5-[5-trifluoroacetyl-thien-2-yl]-1, 2, 4-oxadiazole is a possible class II human histone deacetylase inhibitor. Group: Biochemicals. Grades: Highly Purified. CAS No. 946499-88-3. Pack Sizes: 2.5mg, 25mg. Molecular Formula: C13H7F3N2O4S3. US Biological Life Sciences. | Worldwide |
| 3-[4-(1,3,4-Oxadiazol-2-yl)phenoxymethyl]-5-[5-trifluoroacetyl-thien-2-yl]-1,2,4-oxadiazole | 3-[4-(1,3,4-Oxadiazol-2-yl)phenoxymethyl]-5-[5-trifluoroacetyl-thien-2-yl]-1,2,4-oxadiazole is a possible class II human histone deacetylase inhibitor. Group: Biochemicals. Grades: Highly Purified. CAS No. 946500-06-7. Pack Sizes: 2.5mg, 25mg. Molecular Formula: C17H9F3N4O4S. US Biological Life Sciences. | Worldwide |
| 3-? ( (4-?Methylpiperazin-?1-?yl) ?methyl) ?benzonitrile | 3-? ( (4-?Methylpiperazin-?1-?yl) ?methyl) ?benzonitrile is involved in the preparation of N- hydroxyphenyl acryl amide s and N-Hydroxypyridin-2-ylacrylamides as novel histone deacetylase inhibitors. Group: Biochemicals. Grades: Highly Purified. CAS No. 859850-90-1. Pack Sizes: 50mg, 100mg. Molecular Formula: C13H17N3, Molecular Weight: 215.29. US Biological Life Sciences. | Worldwide |
| 3-Bromo-4- (methoxymethoxy) benzaldehyde | 3-Bromo-4- (methoxymethoxy) benzaldehyde is an intermediate in synthesizing CARM1-IN-1 Hydrochloride (C183610), a mixed Histone/Protein Methyltransferase, Acetyltransferase, and Class III Deacetylase (Sirtuin) inhibitor. Group: Biochemicals. Grades: Highly Purified. CAS No. 162269-90-1. Pack Sizes: 50mg, 100mg. Molecular Formula: C9H9BrO3. US Biological Life Sciences. | Worldwide |
| 3-Pyridinemethanol | 3-Pyridinemethanol, an aromatic alcohol compound, is a widely used in the synthesis of some inhibitors like Chk1 and histone deacetylase inhibitors. Uses: 3-pyridinemethanol is a widely used in the synthesis of some inhibitors like chk1 and histone deacetylase inhibitors. Synonyms: pyridin-3-ylmethanol. Grades: 95 %. CAS No. 100-55-0. Molecular formula: C6H7NO. Mole weight: 109.13. | |
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