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| Product | Description | |
|---|---|---|
| BCH | BCH (2-Amino-2-norbornanecarboxylic acid) is a selective and competitive inhibitor of large neutral amino acid transporter 1 (LAT1) significantly inhibit cellular uptake of amino acids and mTOR phosphorylation, which induces the suppression of cancer growth and apoptosis [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: 2-Amino-2-norbornanecarboxylic acid; LAT1-IN-1. CAS No. 20448-79-7. Pack Sizes: 10 mM * 1 mL; 50 mg; 100 mg. Product ID: HY-108540. |  |
| BCH | BCH. Group: Biochemicals. Grades: Purified. CAS No. 20448-79-7. Pack Sizes: 50mg. US Biological Life Sciences. |  Worldwide |
| BCH | BCH is an inhibitor of L-type amino acid transporter (LAT1), which is a therapeutic target for human esophageal squamous cell carcinoma. BCH inhibits growth and induces apoptosis via activation of caspases in KB, Saos2 and C6 cancer cell lines. Synonyms: 2-Aminobicyclo[2.2.1]heptane-2-carboxylic acid. CAS No. 20448-79-7. Molecular formula: C8H13NO2. Mole weight: 155.2. |  |
| BCH001 | BCH001, a quinoline derivative, is a specific PAPD5 inhibitor. BCH001 restores telomerase activity and telomere length in dyskeratosis congenita (DC) induced pluripotent stem cells. BCH001 shows no inhibition of poly(A)-specific ribonuclease (PARN) or several other canonical and non-canonical polynucleotide polymerases. BCH001 is used to regulate aging[1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 384859-58-9. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-137817. | |
| BCH001 | BCH001 is a specific PAPD5 inhibitor. BCH001 restores telomerase activity and telomere length in DC patient induced pluripotent stem cells. Synonyms: 2-((3-(Ethoxycarbonyl)-6-(trifluoromethoxy)quinolin-4-yl)amino)benzoicacid. CAS No. 384859-58-9. Molecular formula: C20H15F3N2O5. Mole weight: 420.34. | |
| BChE-IN-17 | BChE-IN-17 (compound 6n) is a potent and selective BChE inhibitor with IC 50 s of 10.5 nM and 32.5 nM for eqBChE and hBChE , respectively. BChE-IN-17 shows over 1000-fold selectivity to BChE against AChE. BChE-IN-17 shows low neurotoxicity and moderate neuroprotective effects [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 2425632-57-9. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-155140. | |
| BChE inhibitor 8012-9656 | BChE inhibitor 8012-9656 is a potent and selective inhibitor of butyrylcholinsterase (BChE). It inhibits BChE in a noncompetitive manner and could occupy the binding pocket forming diverse interactions with the target. Synonyms: 2-(2-(4-Amino-1,2,5-oxadiazol-3-yl)-1H-benzo[d]imidazol-1-yl)-N-(2-methylquinolin-6-yl)acetamide. Grade: 98%. CAS No. 446266-84-8. Molecular formula: C21H17N7O2. Mole weight: 399.41. | |
| Amino-2,6,6-Me3-BCheptane-COOH HCl(R,R,S,R) | Amino-2,6,6-Me3-BCheptane-COOH HCl(R,R,S,R). Synonyms: (1R,2R,3S,5R)-2-amino-2,6,6-trimethylbicyclo[3.1.1]heptane-3-carboxylic acid hydrochloride. Molecular formula: C11H19NO2·HCl. Mole weight: 233.73. | |
| Amino-2,6,6-Me3-BCheptane-COOH HCl(S,S,R,S) | Amino-2,6,6-Me3-BCheptane-COOH HCl(S,S,R,S). Synonyms: (1S,2S,3R,5S)-2-amino-2,6,6-trimethylbicyclo[3.1.1]heptane-3-carboxylic acid hydrochloride. Molecular formula: C11H19NO2·HCl. Mole weight: 233.73. | |
| Amino-2,6,6-Me3-BCheptane-COOH(R,R,S,R) | Amino-2,6,6-Me3-BCheptane-COOH(R,R,S,R). Synonyms: (1R,2R,3S,5R)-2-amino-2,6,6-trimethylbicyclo[3.1.1]heptane-3-carboxylic acid. CAS No. 705948-99-8. Molecular formula: C11H19NO2. Mole weight: 197.27. | |
| Amino-2,6,6-Me3-BCheptane-COOH(S,S,R,S) | Amino-2,6,6-Me3-BCheptane-COOH(S,S,R,S). Synonyms: (1S,2S,3R,5S)-2-amino-2,6,6-trimethylbicyclo[3.1.1]heptane-3-carboxylic acid. CAS No. 705949-10-6. Molecular formula: C11H19NO2. Mole weight: 197.27. | |
| (Amino-3,3-Me2-BChept-2-yl)acetic acid HCl(R,S,S) | (Amino-3,3-Me2-BChept-2-yl)acetic acid HCl(R,S,S). Synonyms: [(1R,2S,4S)-2-amino-3,3-dimethylbicyclo[2.2.1]hept-2-yl]acetic acid hydrochloride. CAS No. 1335031-66-7. Molecular formula: C11H19NO2·HCl. Mole weight: 233.73. | |
| (Amino-3,3-Me2-BChept-2-yl)acetic acid(R,S,S) | (Amino-3,3-Me2-BChept-2-yl)acetic acid(R,S,S). Synonyms: [(1R,2S,4S)-2-amino-3,3-dimethylbicyclo[2.2.1]hept-2-yl]acetic acid. Molecular formula: C11H19NO2. Mole weight: 197.27. | |
| Amino-4,7,7-Me3-BCheptane-COOH HCl(R,R,S,S) | Amino-4,7,7-Me3-BCheptane-COOH HCl(R,R,S,S). Synonyms: (1R,3R,4S,6S)-4-amino-4,7,7-trimethylbicyclo[4.1.0]heptane-3-carboxylic acid hydrochloride. Molecular formula: C11H19NO2·HCl. Mole weight: 233.73. | |
| Amino-4,7,7-Me3-BCheptane-COOH(R,R,S,S) | Amino-4,7,7-Me3-BCheptane-COOH(R,R,S,S). Synonyms: (1R,3R,4S,6S)-4-amino-4,7,7-trimethylbicyclo[4.1.0]heptane-3-carboxylic acid. Molecular formula: C11H19NO2. Mole weight: 197.27. | |
| (Amino-6,6-Me2-BChept-2-yl)acetic acid HCl(R,S,S) | (Amino-6,6-Me2-BChept-2-yl)acetic acid HCl(R,S,S). Synonyms: [(1R,2S,5S)-2-amino-6,6-dimethylbicyclo[3.1.1]hept-2-yl]acetic acid hydrochloride. CAS No. 1335031-82-7. Molecular formula: C11H19NO2·HCl. Mole weight: 233.73. | |
| (Amino-6,6-Me2-BChept-2-yl)acetic acid(R,S,S) | (Amino-6,6-Me2-BChept-2-yl)acetic acid(R,S,S). Synonyms: [(1R,2S,5S)-2-amino-6,6-dimethylbicyclo[3.1.1]hept-2-yl]acetic acid. CAS No. 1335093-14-5. Molecular formula: C11H19NO2. Mole weight: 197.27. | |
| Amino-BChept-5-ene-COOH HCl(R,R,S,S/S,S,R,R) | Amino-BChept-5-ene-COOH HCl(R,R,S,S/S,S,R,R). Synonyms: (1R,2R,3S,4S/1S,2S,3R,4R)-3-aminobicyclo[2.2.1]hept-5-ene-2-carboxylic acid hydrochloride. CAS No. 53623-52-2. Molecular formula: C8H11NO2·HCl. Mole weight: 189.64. | |
| Amino-BChept-5-ene-COOH(R,R,S,S/S,S,R,R) | Amino-BChept-5-ene-COOH(R,R,S,S/S,S,R,R). Synonyms: (1R,2R,3S,4S/1S,2S,3R,4R)-3-aminobicyclo[2.2.1]hept-5-ene-2-carboxylic acid. Molecular formula: C8H11NO2. Mole weight: 153.18. | |
| Amino-BCheptane-COOH HCl(S,R,S,R/R,S,R,S) | Amino-BCheptane-COOH HCl(S,R,S,R/R,S,R,S). Synonyms: (1S,2R,3S,4R/1R,2S,3R,4S)-3-aminobicyclo[2.2.1]heptane-2-carboxylic acid hydrochloride (1:1); (CIS)-2-AMINO-3-CARBOXYBICYCLO[2.2.1]HEPTANE HYDROCHLORIDE. CAS No. 14932-25-3. Molecular formula: C8H13NO2HCl. Mole weight: 191.66. | |
| Amino-BCheptane-COOH(S,R,S,R/R,S,R,S) | Amino-BCheptane-COOH(S,R,S,R/R,S,R,S). Synonyms: (1S,2R,3S,4R/1R,2S,3R,4S)-3-aminobicyclo[2.2.1]heptane-2-carboxylic acid; 3-Amino-bicyclo[2.2.1]heptane-2-carboxylic acid; 3-Amino-2-norbornanecarboxylic acid. Grade: ≥ 95%. CAS No. 76198-36-2. Molecular formula: C8H13NO2. Mole weight: 155.19. | |
| Boc-NH-2,6,6-Me3-BCheptane-COOH(S,S,R,S) | Boc-NH-2,6,6-Me3-BCheptane-COOH(S,S,R,S). Synonyms: N-Boc (1S,2S,3R,5S)-2-amino-2,6,6-trimethylbicyclo[3.1.1]heptane-3-carboxylic acid; (1S,2S,3R,5S)-2-[(tert-butoxycarbonyl)amino]-2,6,6-trimethylbicyclo[3.1.1]heptane-3-carboxylic acid. CAS No. 705949-07-1. Molecular formula: C16H27NO4. Mole weight: 297.39. | |
| (Boc-NH-7,7-Me2-BChept-3-yl]acetic acid(R,R,S,S) | (Boc-NH-7,7-Me2-BChept-3-yl]acetic acid(R,R,S,S). Synonyms: (1R,3R,4S,6S)-4-[(tert-butoxycarbonyl)amino]-4,7,7-trimethylbicyclo[4.1.0]heptane-3-carboxylic acid. CAS No. 654680-62-3. Molecular formula: C16H27NO4. Mole weight: 297.39. | |
| Boc-NH-cis-BCheptane-COOH | Boc-NH-cis-BCheptane-COOH. Synonyms: (1S,2R,3S,4R/1R,2S,3R,4S)-3-[(tert-butoxycarbonyl)amino]bicyclo[2.2.1]heptane-2-carboxylic acid; BOC-3-EXO-AMINOBICYCLO[2.2.1]HEPTANE-2-EXO-CARBOXYLIC ACID. Grade: ≥ 95%. CAS No. 1212373-01-7. Molecular formula: C13H21NO4. Mole weight: 255.31. | |
| Boc-NH-cis-BCheptene-COOH | Boc-NH-cis-BCheptene-COOH. Synonyms: (1S,2S,3R,4R/1R,2R,3S,4S)-3-[(tert-butoxycarbonyl)amino]bicyclo[2.2.1]hept-5-ene-2-carboxylic acid; BOC-3-EXO-AMINOBICYCLO[2.2.1]HEPT-5-ENE-2-EXO-CARBOXYLIC ACID; DIEXO-3-TERT-BUTOXYCARBONYLAMINO-BICYCLO[2.2.1]HEPT-5-ENE-2-CARBOXYLIC ACID. Grade: 95%. CAS No. 148257-06-1. Molecular formula: C13H19NO4. Mole weight: 253.29. | |
| Butyrylcholinesterase (BCHE), Horse Serum | Butyrylcholinesterase (BCHE), Horse Serum (BCHE, BuChE, PCHE, pseudocholinesterase, plasma cholinesterase, Acylcholine acyl-hydrolase, Choline esterase, butyryl) is a biological material or organic compound that can be used in life science research[1][2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: BCHE, BuChE, PCHE, pseudocholinesterase, plasma cholinesterase, Acylcholine acyl-hydrolase, Choline esterase, butyryl. Pack Sizes: 200 U; 500 U. Product ID: HY-E70362. | |
| Fmoc-NH-2,6,6-Me3-BCheptane-COOH(R,R,S,R) | Fmoc-NH-2,6,6-Me3-BCheptane-COOH(R,R,S,R). Synonyms: (1R,2R,3S,5R)-2-{[(9H-fluoren-9-ylmethoxy)carbonyl]amino}-2,6,6-trimethylbicyclo[3.1.1]heptane-3-carboxylic acid. CAS No. 1335031-79-2. Molecular formula: C26H29NO4. Mole weight: 419.5. | |
| Fmoc-NH-2,6,6-Me3-BCheptane-COOH(S,S,R,S) | Fmoc-NH-2,6,6-Me3-BCheptane-COOH(S,S,R,S). Synonyms: (1S,2S,3R,5S)-2-{[(9H-fluoren-9-ylmethoxy)carbonyl]amino}-2,6,6-trimethylbicyclo[3.1.1]heptane-3-carboxylic acid; N-Fmoc-(1S,2S,3R,5S)-2-amino-2,6,6-trimethylbicyclo[3.1.1]heptane-3-carboxylic acid. CAS No. 1335031-88-3. Molecular formula: C26H29NO4. Mole weight: 419.5. | |
| (Fmoc-NH-3,3-Me2-BChept-2-yl)acetic acid(R,S,S) | (Fmoc-NH-3,3-Me2-BChept-2-yl)acetic acid(R,S,S). Synonyms: [(1R,2S,4S)-2-{[(9H-fluoren-9-ylmethoxy)carbonyl]amino}-3,3-dimethylbicyclo[2.2.1]hept-2-yl]acetic acid. CAS No. 1335031-67-8. Molecular formula: C26H29NO4. Mole weight: 419.5. | |
| (Fmoc-NH-6,6-Me2-BChept-2-yl)acetic acid(R,S,S) | (Fmoc-NH-6,6-Me2-BChept-2-yl)acetic acid(R,S,S). Synonyms: N-Fmoc-[(1R,2S,5S)-2-amino-6,6-dimethylbicyclo[3.1.1]hept-2-yl]acetic acid; [(1R,2S,5S)-2-{[(9H-fluoren-9-ylmethoxy)carbonyl]amino}-6,6-dimethylbicyclo[3.1.1]hept-2-yl]acetic acid. CAS No. 1335031-68-9. Molecular formula: C26H29NO4. Mole weight: 419.5. | |
| (Fmoc-NH-7,7-Me2-BChept-3-yl)acetic acid(R,R,S,S) | (Fmoc-NH-7,7-Me2-BChept-3-yl)acetic acid(R,R,S,S). Synonyms: (1R,3R,4S,6S)-4-{[(9H-fluoren-9-ylmethoxy)carbonyl]amino}-4,7,7-trimethylbicyclo[4.1.0]heptane-3-carboxylic acid. CAS No. 1335034-84-8. Molecular formula: C26H29NO4. Mole weight: 419.5. | |
| Fmoc-NH-cis-BCheptane-COOH | Fmoc-NH-cis-BCheptane-COOH. Synonyms: (1S,2R,3S,4R/1R,2S,3R,4S)-3-{[(9H-fluoren-9-ylmethoxy)carbonyl]amino}bicyclo[2.2.1]heptane-2-carboxylic acid; Fmoc-3-exo-aminobicyclo[2.2.1]-heptane-2-exo-carboxylic acid; 3-(9H-fluoren-9-ylmethoxycarbonylamino)bicyclo[2.2.1]heptane-2-carboxylic acid. Grade: ≥ 99% (HPLC). CAS No. 352707-75-6. Molecular formula: C23H23NO4. Mole weight: 377.43. | |
| Fmoc-NH-cis-BCheptene-COOH | Fmoc-NH-cis-BCheptene-COOH. Synonyms: (1S,2S,3R,4R/1R,2R,3S,4S)-3-{[(9H-fluoren-9-ylmethoxy)carbonyl]amino}bicyclo[2.2.1]hept-5-ene-2-carboxylic acid. CAS No. 1217848-39-9. Molecular formula: C23H21NO4. Mole weight: 375.4. | |
| Lamivudine (3TC, (-)-BCH-189, 3-Thia-2,3-dideoxycytidine) | A reverse transcriptase inhibitor. Group: Biochemicals. Alternative Names: 3TC, (-)-BCH-189, 3-Thia-2,3-dideoxycytidine. Grades: Highly Purified. Pack Sizes: 25mg. US Biological Life Sciences. | Worldwide |
| PSMA-BCH | PSMA-BCH (NOTA-PSMA) is a NOTA-conjugated precursor. NOTA is a bifunctional chelate which acts as the framework to construct PET imaging tools [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: NOTA-PSMA. CAS No. 1703768-73-3. Pack Sizes: 5 mg; 10 mg. Product ID: HY-155483. | |
| 2',3'-Dideoxy-3'-thiacytidine | An enantiomer of Lamivudine, which is a potent nucleoside analog reverse transcriptase inhibitor, used for the treatment of chronic HBV and HIV/AIDS. Synonyms: Lamivudine Impurity D (Lamivudine Enantiomer); 4-Amino-1-[(2S,5R)-2-(hydroxymethyl)-1,3-oxathiolan-5-yl]pyrimidin-2(1H)-one; 4-Amino-1-[(2S,5R)-2-(hydroxymethyl)-1,3-oxathiolan-5-yl]-2(1H)-pyrimidinone; (2S-cis)-4-Amino-1-[2-(hydroxymethyl)-1,3-oxathiolan-5-yl]-2(1H)-pyrimidinone; (+)-BCH 189; Lamivudine EP Impurity D; 2'-Deoxy-3'-thiacytidine; 3TC; NSC 620753; cis(+)-2-Hydroxymethyl-5-(cytosin-1-yl)-1,3-oxathiolane; ent-Lamivudine; (+)-cis-Lamivudine. Grade: 95%. CAS No. 134680-32-3. Molecular formula: C8H11N3O3S. Mole weight: 229.26. | |
| 3-Hydroxy Anagrelide-[13C3] | 3-Hydroxy Anagrelide-[13C3] is the labelled analogue of 3-Hydroxy Anagrelide, which is a metabolite of Anagrelide. Anagrelide is a medication used for the treatment of essential thrombocytosis (ET). Synonyms: 3-Hydroxy Anagrelide-13C3; 6,7-Dichloro-1,5-dihydro-3-hydroxyimidazo[2,1-b]quinazolin-2(3H)-one-13C3; BCH 24426-13C3. Grade: >95%. CAS No. 1219393-12-0. Molecular formula: C7[13C]3H7Cl2N3O2. Mole weight: 275.06. | |
| 4-Hydroxyisophthalic acid | 4-Hydroxyisophthalic acid activates antioxidant enzymes (such as catalase CAT and superoxide dismutase SOD ), scavenges free radicals, and exhibits antioxidant property. 4-Hydroxyisophthalic acid activates AChE and BChE , enhances neuronal function and improves Tau-induced neurobehavioral defects. 4-Hydroxyisophthalic acid improves the cognitive defects, and ameliorates circadian rhythm disorders of fruit flies [1]. Uses: Scientific research. Group: Natural products. CAS No. 636-46-4. Pack Sizes: 10 mM * 1 mL; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-76632. | |
| 4'-(trans-4-Propylcyclohexyl)-3,4-difluorobiphenyl | 4'-(trans-4-Propylcyclohexyl)-3,4-difluorobiphenyl. Group: Liquid crystal (lc) materials. Alternative Names: trans-4'(4-n-Propylcyclohexyl)-3,4-difluor-1,1'-biphenyl(bch-3f.f); 4''-(TRANS-4-PROPYLCYCLOHEXYL)-3,4-DIFLUOROBIPHENYL. CAS No. 85312-59-0. Product ID: 1,2-difluoro-4-[4-(4-propylcyclohexyl)phenyl]benzene. Molecular formula: 314.417. Mole weight: C21< / sub>H24< / sub>F2< / sub>. VULXHDGYVHCLLN-UHFFFAOYSA-N. 98%. |  |
| ACG548B | ACG548B is a potent inhibitor of acetyl- and butyrylcholinesterase (AChE and BChE) with IC50s of 1.78 and 0.496 μM, respectively. It has higher AChE affinity and selectivity over BChE and ChoK (choline kinase). Synonyms: ACG-548B; 1,1'-([1,1'-biphenyl]-3,3'-diylbis(methylene))bis(4-((4-chlorophenyl)(methyl)amino)pyridin-1-ium) bromide. CAS No. 795316-16-4. Molecular formula: C38H34Br2Cl2N4. Mole weight: 777.42. | |
| Apricitabine | Apricitabine is a highly selective and orally active HIV-1 reverse transcriptase (RT) inhibitor (Ki = 0.08 μM), with Kis of 300, 12 and 112.25 μM against DNA polymerase α, β and γ, respectively. It has been used in trials studying the treatment of HIV Infections. Synonyms: Apricitabine; 160707-69-7; AVX754; AVX-754; SPD754; Apricitabine [INN]; BCH 10618; BCH-10618; SPD-754; (-)-dOTC; 4-Amino-1-((2R,4R)-2-(hydroxymethyl)-1,3-oxathiolan-4-yl)pyrimidin-2(1H)-one; 4-amino-1-[(2R,4R)-2-(hydroxymethyl)-1,3-oxathiolan-4-yl]pyrimidin-2-one; K1YX059ML1; SPD -754; BCH-10619; BCH-10652; BCH-10652, (-)-; AVX 754; (-)-2'-Deoxy-3'-oxa-4'-thiocytidine (apricitabine); 2(1H)-Pyrimid. Grade: 95%. CAS No. 160707-69-7. Molecular formula: C8H11N3O3S. Mole weight: 229.26. | |
| bacteriochlorophyll a synthase | The enzyme catalyses the addition of a geranylgeranyl hydrophobic chain to bacteriochlorophyllide a via an ester bond with the 17-propionate residue. The side chain is later modified to a phytyl chain, resulting in bacteriochlorophyll a. Group: Enzymes. Synonyms: bchG (gene name). Enzyme Commission Number: EC 2.5.1.133. 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-2749; bacteriochlorophyll a synthase; EC 2.5.1.133; bchG (gene name). Cat No: EXWM-2749. |  |
| bacteriochlorophyllide a dehydrogenase | The enzyme, together with EC 1.3.7.15, chlorophyllide-a reductase, and EC 4.2.1.165, chlorophyllide-a 31-hydratase, is involved in the conversion of chlorophyllide a to bacteriochlorophyllide a. The enzymes can act in multiple orders, resulting in the formation of different intermediates, but the final product of the cumulative action of the three enzymes is always bacteriochlorophyllide a. The enzyme oxidizes a hydroxyl group on ring A, converting it to an oxo group. Group: Enzymes. Synonyms: bchC (gene name). Enzyme Commission Number: EC 1.1.1.396. 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-0316; bacteriochlorophyllide a dehydrogenase; EC 1.1.1.396; bchC (gene name). Cat No: EXWM-0316. | |
| Benactyzine hydrochloride | Benactyzine hydrochloride is a competitive BChE inhibitor with a K i of 0.01 mM. Benactyzine hydrochloride is an anticholinergic drug. Benactyzine hydrochloride has the potential for organophosphate poisoning research [1] [2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 57-37-4. Pack Sizes: 10 mM * 1 mL; 100 mg. Product ID: HY-B1542A. | |
| Benactyzine hydrochloride | Benactyzine is an antagonist of acetylcholine in the central and peripheral nervous system. Benactyzine is used as an antispasmodic. Benactyzine hydrochloride is also a butyrylcholinesterase (BChE) inhibitor with a Ki of 0.010 mM. Uses: Parasympatholytics. Synonyms: EA 2092; EA-2092; EA2092; Suavitil; Phebex; Phobex; Cedad; Cevanol; Deprol; Lucidil; Morcain; Nutinal; Parasan. Grade: ≥98%. CAS No. 57-37-4. Molecular formula: C20H25NO3·HCl. Mole weight: 363.88. | |
| chlorophyllide a 31-hydratase | The enzyme, together with EC 1.3.7.15, chlorophyllide-a reductase, and EC 1.1.1.396, bacteriochlorophyllide-a dehydrogenase, is involved in the conversion of chlorophyllide a to bacteriochlorophyllide a. The enzymes can act in multiple orders, resulting in the formation of different intermediates, but the final product of the cumulative action of the three enzymes is always bacteriochlorophyllide a. The enzyme catalyses the hydration of a vinyl group on ring A, converting it to a hydroxyethyl group. Group: Enzymes. Synonyms: bchF (gene name). Enzyme Commission Number: EC 4.2.1.165. 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-5006; chlorophyllide a 31-hydratase; EC 4.2.1.165; bchF (gene name). Cat No: EXWM-5006. | |
| chlorophyllide a reductase | The enzyme, together with EC 1.1.1.396, bacteriochlorophyllide-a dehydrogenase, and EC 4.2.1.165, chlorophyllide-a 31-hydratase, is involved in the conversion of chlorophyllide a to bacteriochlorophyllide a. These enzymes can act in multiple orders, resulting in the formation of different intermediates, but the final product of the cumulative action of the three enzymes is always bacteriochlorophyllide a. This enzyme catalyses a trans-reduction of the B-ring; the product has the (7R,8R)-configuration. In addition, the enzyme has a latent activity of EC 1.3.7.13, 3,8-divinyl protochlorophyllide a 8-vinyl-reductase (ferredoxin). The enzyme contains a [4Fe-4S] cluster, and structurally resembles the Fe protein/MoFe protein complex of nitrogenase (EC 1.18.6.1), which catalyses an ATP-driven reduction. Group: Enzymes. Synonyms: bchX (gene name); bchY (gene name); bchZ (gene name); COR. Enzyme Commission Number: EC 1.3.7.15. 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-1396; chlorophyllide a reductase; EC 1.3.7.15; bchX (gene name); bchY (gene name); bchZ (gene name); COR. Cat No: EXWM-1396. | |
| cholinesterase | Acts on a variety of choline esters and a few other compounds. Group: Enzymes. Synonyms: pseudocholinesterase; butyrylcholine esterase; non-specific cholinesterase; choline esterase II (unspecific); benzoylcholinesterase; choline esterase; butyrylcholinesterase; propionylcholinesterase; BtChoEase. Enzyme Commission Number: EC 3.1.1.8. CAS No. 9001-8-5. BCHE. 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-3508; cholinesterase; EC 3.1.1.8; 9001-08-5; pseudocholinesterase; butyrylcholine esterase; non-specific cholinesterase; choline esterase II (unspecific); benzoylcholinesterase; choline esterase; butyrylcholinesterase; propionylcholinesterase; BtChoEase. Cat No: EXWM-3508. | |
| Cholinesterase, Horse serum | Cholinesterase, Horse serum infers to acetylcholinesterase (AChE) and butyryl cholinesterase (BChE). AChE and BChE catalyze the hydrolysis of 6-MAM to morphine [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: EC 3.1.1.8; BCHE, Horse serum. CAS No. 9001-8-5. Pack Sizes: 100 U. Product ID: HY-P2798. | |
| Cimifugin | Cimifugin, isolated from Peucedanum schottii, displays low to moderate inhibition towards AChE and BChE (3.12 and 21.63%, respectively) at 200ug ml-1.[1]Cimifugin appears to inhibit FITC-induced type 2 allergic contact dermatitis and its mechanism might be related to regulating the balance of Th1 /Th2 by inhibiting type 2 cytokines.[2]. Group: Biochemicals. Alternative Names: 2,3-Dihydro-4-methoxy-7-(hydroxymethyl)-2-(1-hydroxy-1-methylethyl)-5H-furo[3,2-g][1]benzopyran-5-one; Cimitin; 1-Naphtyl β-D-galactopyranoside. Grades: Highly Purified. CAS No. 37921-38-3. Pack Sizes: 5mg, 10mg, 25mg. Molecular Formula: C16H18O6, Molecular Weight: 306.31. US Biological Life Sciences. | Worldwide |
| cis-(±)-2-Hydroxymethyl-5-(cytosin-1-yl)-1,3-oxathiolane | cis-(±)-2-Hydroxymethyl-5-(cytosin-1-yl)-1,3-oxathiolane is a derivative of Lamivudine, which is a potent nucleoside analog reverse transcriptase inhibitor, used for the treatment of chronic HBV and HIV/AIDS. Synonyms: 2(1H)-Pyrimidinone, 4-amino-1-[(2R,5S)-2-(hydroxymethyl)-1,3-oxathiolan-5-yl]-, rel-; 1,3-Oxathiolane, 2(1H)-pyrimidinone deriv.; 2(1H)-Pyrimidinone, 4-amino-1-[2-(hydroxymethyl)-1,3-oxathiolan-5-yl]-, cis-(±)-; 2(1H)-Pyrimidinone, 4-amino-1-[2-(hydroxymethyl)-1,3-oxathiolan-5-yl]-, cis-; BCH 189. Grade: ≥95%. CAS No. 131086-21-0. Molecular formula: C8H11N3O3S. Mole weight: 229.26. | |
| Coumarin 106 | Coumarin 106 (Coumarin 478) is a dipolar laser dye. Coumarin 106 is an inhibitor of AChE and BChE. Coumarin 106 displays mixed-type AChE inhibition with a pIC 50 =4.97 and K i =2.36 μM. Coumarin 106 inhibits BChE with slightly lower potency ( pIC 50 =4.56) [1] [2]. Uses: Scientific research. Group: Fluorescent dye. Alternative Names: Coumarin 478. CAS No. 41175-45-5. Pack Sizes: 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-W324391. | |
| Drofenine hydrochloride | Drofenine hydrochloride is a widely used anticholinergic acts on smooth muscle to stop muscle spasms. Uses: A potent competitive inhibitor of bche. Synonyms: 2-(diethylamino)ethyl 2-cyclohexyl-2-phenylacetate; hydrochloride; α-Cyclohexyl-benzeneacetic Acid 2-(Diethylamino)ethyl Ester Hydrochloride. Grade: ≥98%. CAS No. 548-66-3. Molecular formula: C20H32ClNO2. Mole weight: 353.93. | |
| ent-Lamivudine | An enantiomer of Lamivudine ; an antiviral that inhibits HIV-reverse transcriptase. Group: Biochemicals. Alternative Names: 4-Amino-1-[(2S,5R)-2-(hydroxymethyl)-1,3-oxathiolan-5-yl]-2(1H)-pyrimidinone; (2S-cis)-4-Amino-1-[2-(hydroxymethyl)-1,3-oxathiolan-5-yl]-2(1H)-pyrimidinone; (+)-BCH 189; 2',3'-Dideoxy-3'-thiacytidine; 2'-Deoxy-3'-thiacytidine; 3TC; NSC 620753; cis(+)-2-Hydroxymethyl-5-(cytosin-1-yl)-1,3-oxathiolane. Grades: Highly Purified. CAS No. 134680-32-3. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Ethopropazine hydrochloride | Ethopropazine (Isothazine) hydrochloride is a potent, selective BChE inhibitor and a poor AChE inhibitor. Ethopropazine hydrochloride is a phenothiazine compound with anticholinergic properties. Ethopropazine hydrochloride can be used for the research of Parkinsons disease [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Isothazine hydrochloride; Lysivane hydrochloride; Parsidol hydrochloride. CAS No. 1094-08-2. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-107922. | |
| Ethyl triphenylphosphoranylidene acetate | Ethyl triphenylphosphoranylidene acetate is a Horner-Wittig reagent generally used in Horner-Wadsworth-Emmons (HWE) reaction. It may act as an inhibitor of cholinesterase that inhibits AChE and BChE. Synonyms: (Carbethoxymethylene)triphenylphosphorane; Triphenylcarbethoxymethylenephosphorane; Ethyl 2-(triphenylphosphoranylidene)acetate. Grade: ≥ 95 %. CAS No. 1099-45-2. Molecular formula: C22H21O2P. Mole weight: 348.37. | |
| Floramultine | Floramultine is an isoquinoline alkaloid originally isolated from C. speciosum. It inhibits butyrylcholinesterase (BChE) and acetylcholinesterase (AChE, Kis = 23.44 and 151.3 μM, respectively). Synonyms: (S)-Floramultine; (S)-Bechuanine; Merenderine. Grade: ≥95%. CAS No. 1354-66-1. Molecular formula: C21H25NO5. Mole weight: 371.43. | |
| Frakefamide | Frakefamide is a peripheral active μ-selective receptor agonist and used as a potent analgesic. Synonyms: BCH-3963; L-Tyrosyl-D-alanyl-L-(4-fluoro)phenylalanyl-L-phenylalanylamide. CAS No. 188196-22-7. Molecular formula: C30H34FN5O5. Mole weight: 563.63. | |
| Garcinol | Garcinol, a polyisoprenylated benzophenone harvested from Garcinia indica , exerts anti-cholinesterase properties towards acetyl cholinesterase (AChE) and butyrylcholinesterase (BChE) with IC 50 s of 0.66 μM and 7.39 μM, respectively [1]. Garcinol also inhibits histone acetyltransferases ( HATs , IC 50 = 7 μM) and p300/CPB-associated factor ( PCAF , IC 50 = 5 μM). Garcinol has anti-inflammatory and anti-cancer activity [2]. Uses: Scientific research. Group: Natural products. CAS No. 78824-30-3. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg. Product ID: HY-107569. | |
| geranylgeranyl-bacteriochlorophyllide a reductase | The enzyme catalyses the successive reduction of the geranylgeraniol esterifying group to phytol, reducing three out of four double bonds, and transforming geranylgeranyl bacteriochlorophyllide a via dihydrogeranylgeranyl bacteriochlorophyllide a and tetrahydrogeranylgeranyl bacteriochlorophyllide a to bacteriochlorophyll a. The enzyme can also accept the pheophytin derivative geranylgeranyl bacteriopheophytin, converting it to bacteriopheophytin a. Group: Enzymes. Synonyms: geranylgeranyl-bacteriopheophytin reductase; bchP (gene name). Enzyme Commission Number: EC 1.3.1.111. 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-1284; geranylgeranyl-bacteriochlorophyllide a reductase; EC 1.3.1.111; geranylgeranyl-bacteriopheophytin reductase; bchP (gene name). Cat No: EXWM-1284. | |
| Imperatorin | Imperatorin is an effective of NO synthesis inhibitor ( IC 50 =9.2 μmol), which also is a BChE inhibitor ( IC 50 =31.4 μmol). Imperatorin is a weak agonist of TRPV1 with EC 50 of 12.6±3.2 μM. Uses: Scientific research. Group: Natural products. Alternative Names: Ammidin. CAS No. 482-44-0. Pack Sizes: 10 mM * 1 mL; 25 mg; 50 mg; 100 mg. Product ID: HY-N0285. | |
| Lamivudine | Lamivudine (BCH-189) is an orally active nucleoside reverse transcriptase inhibitor (NRTI). Lamivudine can inhibit HIV reverse transcriptase 1/2 and also the reverse transcriptase of hepatitis B virus. Lamivudine salicylate can penetrate the CNS [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: BCH-189. CAS No. 134678-17-4. Pack Sizes: 10 mM * 1 mL; 100 mg; 500 mg. Product ID: HY-B0250. | |
| Lamivudine | Lamivudine (BCH-189) is an orally active nucleoside reverse transcriptase inhibitor (NRTI). Lamivudine can inhibit HIV reverse transcriptase 1/2 and also the reverse transcriptase of hepatitis B virus. Lamivudine salicylate can penetrate the CNS. Uses: Designed for use in research and industrial production. Additional or Alternative Names: (-)-BCH-189;(-)-BETA-L-2,3-DIDEOXY-3-THIACYTIDINE;(-)-B-L-2,3-DIDEOXY-3-THIACYTIDINE;(2r-cis)-4-amino-1-[2-(hydroxymethyl)-1,3-oxathiolan-5-yl]-2(1h)-pyrimidinone;2-deoxy-3-thiacytidine;4-AMINO-1-((2R,5S)-2-HYDROXYMETHYL-[1,3]OXATHIOLAN-5-YL)-1H-PYRIMIDIN-2-ONE;3TC;3-THIA-2,3-DIDEOXYCYTIDINE. Product Category: Inhibitors. Appearance: Solid. CAS No. 134678-17-4. Molecular formula: C8H11N3O3S. Mole weight: 229.26. Purity: 0.9985. Canonical SMILES: OC[C@H]1SC[C@@H](N2C(N=C(N)C=C2)=O)O1. Product ID: ACM134678174. Alfa Chemistry ISO 9001:2015 Certified. |  |
| Lamivudine | Lamivudine. Group: Biochemicals. Alternative Names: 3TC; 2',3'-Dideoxy-3'-thiacytidine; (-)-BCH-189. Grades: Highly Purified. CAS No. 134678-17-4. Pack Sizes: 5g, 10g, 25g, 50g, 100g. Molecular Formula: C8H11N3O3S. US Biological Life Sciences. | Worldwide |
| Lamivudine | Lamivudine is a potent nucleoside analog reverse transcriptase inhibitor, used for treatment of chronic HBV and HIV/AIDS. Synonyms: GR109714X; Epivir; Zeffix; Heptovir; BCH-189; BCH 189; BCH189. Grade: >98%. CAS No. 134678-17-4. Molecular formula: C8H11N3O3S. Mole weight: 229.26. | |
| Lamivudine salicylate | Lamivudine (BCH-189) salicylate is an orally active nucleoside reverse transcriptase inhibitor (NRTI). Lamivudine salicylate can inhibit HIV reverse transcriptase 1/2 and also the reverse transcriptase of hepatitis B virus. Lamivudine salicylate can penetrate the CNS. Uses: Designed for use in research and industrial production. Additional or Alternative Names: (2r-cis)-4-amino-1-[2-(hydroxymethyl)-1,3-oxathiolan-5-yl]-2(1h)-pyrimidinone 2-hydroxybenzoate;lamivudine salicylate;2r-(Hydroxymethyl)-5(S)-Cytosin-1-Yl-1,3-Oxathiolanesalicycic Acid Salt;2R-(hydroxymethyl)-5(s)-cytosin-1-yl-[1,3]-oxathiolane salicylic. Product Category: Inhibitors. CAS No. 173522-96-8. Molecular formula: C8H11N3O3S?C7H6O3. Mole weight: 367.38. Canonical SMILES: OC[C@H]1SC[C@@H](N2C(N=C(N)C=C2)=O)O1.OC3=C(C(O)=O)C=CC=C3. Product ID: ACM173522968. Alfa Chemistry ISO 9001:2015 Certified. Categories: Benzoic acid. | |
| Lamivudine (Standard) | Lamivudine (Standard) is the analytical standard of Lamivudine. This product is intended for research and analytical applications. Lamivudine (BCH-189) is an orally active nucleoside reverse transcriptase inhibitor (NRTI). Lamivudine can inhibit HIV reverse transcriptase 1/2 and also the reverse transcriptase of hepatitis B virus. Lamivudine salicylate can penetrate the CNS [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: BCH-189 (Standard). CAS No. 134678-17-4. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-B0250R. | |
| Native Equine Butyrylcholinesterase | Butyrylcholinesterase (BChE) is a serine hydrolase that is structurally similar to acetylcholinesterase (AChE), but differs in substRate specificities and inhibitor sensitivities. BChE can, unlike AChE, efficiently hydrolyze larger esters of choline such as butyrylcholine and benzoylcholine. The enzyme is a tetrameric glycoprotein with four equal subunits (110 kDa each). The enzyme is activated by Ca2+ and Mg2+ and the activity is constant over the pH range 6.0-8.0. It is inhibited by Betaine, nicotine, organophosphates, carbamates. This product is prepared from equine serum using ammonium sulfate fractionation and supplied as a lyophilized powder. Applications: Butyrylchol...vestigations into selective inhibitors may provide a clearer picture of the physiological role of bche in both healthy and diseased individuals. this product has been used for the screening of cholineesterase inhibitors in selected fruits and vegetables, for restoring cognitive function and improving memory. it has also been used to develop a butyrylcholinesterase and choline oxidase immobilized bio-sniffer for the detection of nicotine. nicotine inhibits bche activity. a decrease in the byproducts of bche activity reflects the volume of nicotine. Group: Enzymes. Synonyms: Butyrylcholinesterase; BCHE; BuChE; pseudocholinesterase; plasma cholinesterase; EC 3.1.1.8; 9001-08-5; | |
| Native Human Butyrylcholinesterase | Butyrylcholinesterase (BChE) is a serine hydrolase that is structurally similar to acetylcholinesterase (AChE), but differs in substRate specificities and inhibitor sensitivities. BChE can, unlike AChE, efficiently hydrolyze larger esters of choline such as butyrylcholine and benzoylcholine. The enzyme is a tetrameric glycoprotein with four equal subunits (110 kDa each). The enzyme is activated by Ca2+ and Mg2+ and the activity is constant over the pH range 6.0-8.0. It is inhibited by Betaine, nicotine, organophosphates, carbamates. Applications: Butyrylcholinesterase (bche) is a serine hydrolase that shares substantial structural similarities with acetylcholinesterase (ache) but has different substrate and inhibitor specificities. bche is found in the serum, hemopoietic cells, liver, lung, heart and the central nervous system of vertebrates. Group: Enzymes. Synonyms: Butyrylcholinesterase; BCHE; BuChE; pseudocholinesterase; plasma cholinesterase; EC 3.1.1.8; 9001-08-5; Acylcholine acyl-hydrolase; Choline esterase; butyryl. Enzyme Commission Number: EC 3.1.1.8. CAS No. 9001-8-5. BCHE. Activity: > 50 U/mg protein. Source: Human serum. Species: Human. Butyrylcholinesterase; BCHE; BuChE; pseudocholinesterase; plasma cholinesterase; EC 3.1.1.8; 9001-08-5; Acylcholine acyl-hydrolase; Choline esterase; butyryl. Cat No: NATE-0093. | |
| N-Boc-[(1R,2S,4S)-2-amino-3,3-dimethylbicyclo[2.2.1]hept-2-yl]acetic acid | N-Boc-[(1R,2S,4S)-2-amino-3,3-dimethylbicyclo[2.2.1]hept-2-yl]acetic acid. Synonyms: (Boc-NH-3,3-Me2-BChept-2-yl)acetic acid(R,S,S); {(1R,2S,4S)-2-[(tert-butoxycarbonyl)amino]-3,3-dimethylbicyclo[2.2.1]hept-2-yl}acetic acid. CAS No. 1335031-80-5. Molecular formula: C16H27NO4. Mole weight: 297.39. | |
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