A directory of where to buy chemicals in the USA, including: distributors, industrial manufacturers, bulk supplies and wholesalers of raw ingredients & finished goods.
Dehydroxy Terfenadine. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 100mg. Molecular Formula: C32H41NO, Molecular Weight: 455.67. US Biological Life Sciences.
Worldwide
Dehydroxytramadol Hydrochloride
Dehydroxytramadol Hydrochloride is an impurity of Tramadol Hydrochloride (T712500), an analgesic. Group: Biochemicals. Grades: Highly Purified. CAS No. 66170-32-9. Pack Sizes: 10mg, 100mg. Molecular Formula: C16H23NO; (HCl), Molecular Weight: 245.363645999999. US Biological Life Sciences.
Worldwide
Dehydrozingerone
Dehydrozingerone (Compound 10), a structural half analogue of Curcumin (HY-N0005), is a phenolic compound with antibacterial, anticancer, antioxidant, anti-Alzheimers and antifungal activity, which is isolated from ginger ( Zingiber officinale ) rhizomes. Dehydrozingerone shows moderate inhibitory activities on the secretion of HBsAg in HepG 2 cells with an IC 50 value of 0.50 mM [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. CAS No. 1080-12-2. Pack Sizes: 5 g; 10 g; 25 g. Product ID: HY-134635.
Deiodo Amiodarone. Uses: For analytical and research use. Group: Impurity standards. Alternative Names: Amiodarone Hydrochloride Imp. C (EP), Amiodarone Hydrochloride Imp. C (EP) as Hydrochloride, Amiodarone Imp. C (EP), (2-Butylbenzofuran-3-yl)[4-[2-(diethylamino)ethoxy]-3-iodo-phenyl]methanone Hydrochloride. Pack Sizes: 10MG. IUPAC Name: (2-butyl-1-benzofuran-3-yl)-[4-[2-(diethylamino)ethoxy]-3-iodophenyl]methanone;hydrochloride. Molecular formula: C25H30INO3.ClH. Mole weight: 555.88. Catalog: APS007355. SMILES: Cl.CCCCc1oc2ccccc2c1C(=O)c3ccc(OCCN(CC)CC)c(I)c3. Format: Neat. Shipping: Room Temperature.
De-Ionised Distilled Water
5lt Pack Size. Group: Analytical Reagents, Solvents, Water Analysis. Formula: H_{2}O. CAS No. 7732-18-5. Prepack ID 34750941-5lt. Molecular Weight 18.0153. See USA prepack pricing.
Deisovalerylblastmycin
Deisovalerylblastmycin is an antimycin antibiotic produced by Streptomyces sp. 5140-A. It has a strong resistance to the rice pear (Magnae grisea) activity, with a MIC of 0.8 μg/mL. Synonyms: Deisovalerylblastmycin; Blastmycin, deisovalery-; N-(7-Butyl-8-hydroxy-4,9-dimethyl-2,6-dioxo-1,5-dioxonan-3-yl)-3-formamidosalicylamide; Salicylamide, N-(7-butyl-4,9-dimethyl-2,6-dioxo-8-hydroxy-1,5-dioxonan-3-yl)-3-formamido-. Grades: >98%. CAS No. 60504-95-2. Molecular formula: C21H28N2O8. Mole weight: 436.45.
DEL22379
DEL22379, also known as NPX800, is ERK dimerization inhibitor. DEL-22379 has been reported to inhibit ERK dimerization which was unaffected by drug-resistant mechanism reactivating the ERK signaling. Uses: Designed for use in research and industrial production. Additional or Alternative Names: DEL22379; DEL-22379; DEL 22379; NPX800; NPX 800; NPX-800. Product Category: Inhibitors. Appearance: To be determined. CAS No. 1693734-80-3. Molecular formula: C26H28N4O3. Mole weight: 444.53. Purity: >98%. IUPACName: N-[2,3-Dihydro-3-[(5-methoxy-1H-indol-3-yl)methylene]-2-oxo-1H-indol-5-yl]-1-piperidinepropanamide. Canonical SMILES: O=C(NC1=CC2=C(NC(/C2=C/C3=CNC4=C3C=C(OC)C=C4)=O)C=C1)CCN5CCCCC5. Product ID: ACM1693734803. Alfa Chemistry ISO 9001:2015 Certified.
DEL-22379
DEL-22379 is a water-soluble ERK dimerization inhibitor with IC50 of ?0.5 μM. Synonyms: DEL-22379; DEL 22379; DEL22379. Grades: 98%. CAS No. 181223-80-3. Molecular formula: C26H28N4O3. Mole weight: 444.53.
Delactamimipenem Monosodium (Mixture of Diastereomers)
Delactamimipenem Monosodium (Mixture of Diastereomers). Group: Biochemicals. Alternative Names: 5-Carboxysodium-3, 4-dihydro-α - (1-hydroxyethyl) -4-[[2-[ (iminomethyl) amino]ethyl]thio]-2H-Pyrrole-2-acetic Acid; Imipenem Amino Acid. Grades: Highly Purified. Pack Sizes: 10mg. Molecular Formula: C12H18N3NaO5S, Molecular Weight: 339.34. US Biological Life Sciences.
Worldwide
Delafloxacin
Delafloxacin is a fluoroquinolone antibiotic that demonstrates extremely high potency against a wide range of bacteria in vitro, including levofloxacin-resistant strains of S. pneumoniae and methicillin-resistant S. aureus. It has an anionic structure, which enhances its potency in acidic environments and in skin and soft tissue infections. Uses: Anti-infective agents. Synonyms: ABT-492; RX-3341; WQ-3034; Abt 492. Grades: 98%. CAS No. 189279-58-1. Molecular formula: C18H12ClF3N4O4. Mole weight: 440.8.
Delafloxacin (RX-3341; WQ-3034; ABT492) is a broad-spectrum fluoroquinolone antibiotic. Delafloxacin has a broad spectrum of activity that includes drug-resistant Staphylococcus aureus , Streptococcus pneumoniae , and Klebsiella pneumonia [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: RX-3341; WQ-3034; ABT492. CAS No. 189279-58-1. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg. Product ID: HY-14814.
delafloxacin meglumine
Delafloxacin meglumine is a fluoroquinolone that can be used to treat acute bacterial skin and skin structure infections (ABSSSI) in adult patients. Studies indicated that it has excellent tolerance and low toxicity to liver and kidney. Uses: The treatment of cute bacterial skin and skin structure infections (absssi). Synonyms: Baxdela; 1-(6-amino-3,5-difluoropyridin-2-yl)-8-chloro-6-fluoro-7-(3-hydroxyazetidin-1-yl)-4-oxoquinoline-3-carboxylic acid;(2R,3R,4R,5S)-6-(methylamino)hexane-1,2,3,4,5-pentol. CAS No. 352458-37-8. Molecular formula: C25H29ClF3N5O9. Mole weight: 635.978.
Delafloxacin meglumine
Delafloxacin meglumine (ABT492 meglumine; RX-3341 meglumine; WQ-3034 meglumine) is a broad-spectrum fluoroquinolone antibiotic. Delafloxacin has a broad spectrum of activity that includes drug-resistant Staphylococcus aureus , Streptococcus pneumoniae , and Klebsiella pneumonia [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: ABT492 meglumine; RX-3341 meglumine; WQ-3034 meglumine. CAS No. 352458-37-8. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-14814A.
Delamanid
25mg Pack Size. Group: Antibiotics, Bioactive Small Molecules, Research Organics & Inorganics. Formula: C25H25F3N4O5. CAS No. 681492-22-8. Prepack ID 90026659-25mg. Molecular Weight 534.48. See USA prepack pricing.
Delamanid
Delamanid is used for the treatment of multi-drug-resistant tuberculosis. It functions by blocking the synthesis of mycolic acids in Mycobacterium tuberculosis, the organism which causes tuberculosis, thus destabilising its cell wall. Uses: The treatment of multi-drug-resistant tuberculosis. Synonyms: OPC-67683; OPC 67683; OPC67683; Deltyba; (2R)-2-methyl-6-nitro-2-[[4-[4-[4-(trifluoromethoxy)phenoxy]piperidin-1-yl]phenoxy]methyl]-3H-imidazo[2,1-b][1,3]oxazole. Grades: ≥98%. CAS No. 681492-22-8. Molecular formula: C25H25F3N4O6. Mole weight: 534.492.
Delamanid
Delamanid, a newer mycobacterial cell wall synthesis inhibitor, inhibits the synthesisi of mucolic acids [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: OPC-67683. CAS No. 681492-22-8. Pack Sizes: 10 mM * 1 mL; 2 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-10846.
Delaminomycin A
Delaminomycin A is an extracellular Matrix receptor antagonist and immunomodulator produced by Streptomyces albulus MJ202-72F3. It inhibits cell adhesion ECM (Extracellular matrix), reduces immune response activity, and inhibits Gram-positive bacteria. Synonyms: 2H-Imidazol-2-one, 3-((2-(2,8-dihydroxy-7-methyl-3,5-decadienyl)-1,2,4a,5,6,7,8,8a-octahydro-1,6,8-trimethyl-1-naphthalenyl)carbonyl)-1,5-dihydro-4,5-dihydroxy-5-methoxy-; 2H-Pyrrol-2-one, 1,5-dihydro-4,5-dihydroxy-3-((2-(2,8-dihydroxy-7-methyl-3,5-decadienyl)-1,2,4a,5,6,7,8,8a-octahydrox-1,6,8-trimethyl-1-naphthalenyl)carbonyl)-. CAS No. 149779-38-4. Molecular formula: C29H43NO6. Mole weight: 501.65.
Delaminomycin B
Delaminomycin B is an extracellular Matrix receptor antagonist and immunomodulator produced by Streptomyces albulus MJ202-72F3. It inhibits cell adhesion ECM (Extracellular matrix), reduces immune response activity, and inhibits Gram-positive bacteria. CAS No. 149779-39-5. Molecular formula: C30H45NO6. Mole weight: 515.68.
Delaminomycin C
Delaminomycin C is an extracellular Matrix receptor antagonist and immunomodulator produced by Streptomyces albulus MJ202-72F3. It inhibits cell adhesion ECM (Extracellular matrix), reduces immune response activity, and inhibits Gram-positive bacteria. Synonyms: (3Z)-3-[[2-[(3E,5E)-2,8-dihydroxy-7-methyldeca-3,5-dienyl]-1,6,8-trimethyl-4a,5,6,7,8,8a-hexahydro-2H-naphthalen-1-yl]-hydroxymethylidene]pyrrolidine-2,4-dione; 2H-Imidazol-2-one, 3-((2-(2,8-dihydroxy-7-methyl-3,5-decadienyl)-1,2,4a,5,6,7,8,8a-octahydro-1,6,8-trimethyl-1-naphthalenyl)carbonyl)-1,5-dihydro-4-hydroxy-. CAS No. 149779-40-8. Molecular formula: C29H43NO5. Mole weight: 485.65.
Delanzomib
Delanzomib is an orally active proteasome inhibitor. Delanzomib has been shown to down-modulate NF-κB, induce apoptosis, inhibit angiogenesis and M-CSF-RANKL-induced osteoclastogenesis. Group: Biochemicals. Alternative Names: [ (1R) -1- [ [ (2S, 3R) -3-Hydroxy-1-oxo-2- [ [ (6-phenyl-2-pyridinyl) carbonyl] amino] butyl] amino] -3-methylbutyl] boronic Acid; CEP 18770; CIP 18770; CT 47098; NPH 007098; [(1R)-1-[[(2S,3R)-3-Hydroxy-2-[[(6-phenylpyridin-2-yl)carbonyl]amino]-1-oxobutyl]amino]-3-methylbutyl]boronic Acid. Grades: Highly Purified. CAS No. 847499-27-8. Pack Sizes: 5mg. US Biological Life Sciences.
Worldwide
Delanzomib
Delanzomib (CEP-18770) is a potent and orally active chymotrypsin-like activity of the proteasome inhibitor with an IC50 of 3.8 nM. Delanzomib inhibits NF-?B activity, induces cancer cell apoptotic, and has strong antiangiogenic and anti-cancer activities[1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: CEP-18770. CAS No. 847499-27-8. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-10454.
Delanzomib
Delanzomib, also known as CEP-18770, is An orally bioavailable synthetic P2 threonine boronic acid inhibitor of the chymotrypsin-like activity of the proteasome, with potential antineoplastic activity. Proteasome inhibitor CEP 18770 represses the proteasomal degradation of a variety of proteins, including inhibitory kappaBalpha (IkappaBalpha), resulting in the cytoplasmic sequestration of the transcription factor NF-kappaB; inhibition of NF-kappaB nuclear translocation and transcriptional up-regulation of a variety of cell growth-promoting factors; and apoptotic cell death in susceptible tumor cell populations. In vitro studies indicate that this agent exhibits a favorable cytotoxicity profile toward normal human epithelial cells, bone marrow progenitors, and bone marrow-derived stromal cells relative to the proteasome inhibitor bortezomib. The intracellular protein IkappaBalpha functions as a primary inhibitor of the proinflammatory transcription factor NF-kappaB. Uses: Proteasome inhibitors. Synonyms: CEP18770; CEP 18770; CEP-18770; Delanzomib. CAS No. 847499-27-8. Molecular formula: C21H28BN3O5. Mole weight: 413.27.
Delapril
Delapril. Uses: Designed for use in research and industrial production. Additional or Alternative Names: DELAPRIL;Alindapril;Glycine, N-(2,3-dihydro-1H-inden-2-yl)-N-[N-[1-(ethoxycarbonyl)-3-phenylpropyl]-L-alanyl]-, (S)-;Glycine, N-[(1S)-1-(ethoxycarbonyl)-3-phenylpropyl]-L-alanyl-N-(2,3-dihydro-1H-inden-2-yl)-;Indalapril;N-[N-[(S)-1-(Ethoxycarbonyl)-3-phe. Product Category: Heterocyclic Organic Compound. CAS No. 83435-66-9. Molecular formula: C26H32N2O5. Mole weight: 452.548. Product ID: ACM83435669. Alfa Chemistry ISO 9001:2015 Certified.
DelapRil HCl
DelapRil HCl. Group: Biochemicals. Grades: Highly Purified. CAS No. 83435-67-0. Pack Sizes: 50mg, 100mg, 250mg, 500mg, 1g. US Biological Life Sciences.
Worldwide
Delapril hydrochloride
Delapril hydrochloride is an angiotensin-converting enzyme ( ACE ) inhibitor for the treatment of cardiovascular diseases [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 83435-67-0. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-107337.
Delapril hydrochloride
Delapril Hydrochloride is the hydrochloride salt form of delapril, which is a lipophilic, non-sulfhydryl angiotensin-converting enzyme (ACE) inhibitor with antihypertensive effect. Synonyms: Alindapril hydrochloride; Delapril HCl; CV 3317; UNII-2SMM3M5ZMH. CAS No. 83435-67-0. Molecular formula: C26H33ClN2O5. Mole weight: 489.
De-(L-Asn)-L-Gln Vancomycin B
An impurity of Vancomycin. Vancomycin is a glycopeptide antibiotic for the treatment of gram-positive bacteria. Vancomycin exhibits an antibacterial effect by inhibiting bacterial cell wall synthesis. Molecular formula: C67H77Cl2N9O24 HCl. Mole weight: 1499.77.
Delavinone
Delavinone is an alkaloid isolated from the bulbs of Fritillaria yuminensis. Synonyms: Puqiedinone; Sinpeinine A; 3-Hydroxycevan-6-one. Grades: >98%. CAS No. 96997-98-7. Molecular formula: C27H43NO2. Mole weight: 413.646.
Delavirdine
Delavirdine (U 90152) is a potent, highly specific and orally active non-nucleoside reverse transcriptase inhibitor (NNRTI). Delavirdine selectively inhibits HIV-1 reverse transcriptase (RT) ( IC 50=0.26 μM) over DNA polymerase α (IC 50=440 μM) and polymerase δ (IC 50 >550 μM). Delavirdine is an inhibitor of HIV-1 replication and can can be used for the study of AIDs [1]. Uses: Scientific research. Group: Natural products. Alternative Names: U 90152; BHAP-U 90152. CAS No. 136817-59-9. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg; 200 mg. Product ID: HY-10571.
Delavirdine
Delavirdine is a non-nucleoside reverse transcriptase inhibitor (NNRTI). It is used as part of highly active antiretroviral therapy (HAART) for the treatment of human immunodeficiency virus (HIV) type 1. Synonyms: U 90152; U90152; U-90152; BHAP-U 90152. Grades: >98%. CAS No. 136817-59-9. Molecular formula: C22H28N6O3S. Mole weight: 456.56.
Delavirdine
Delavirdine. Group: Biochemicals. Alternative Names: N-[2-[[4-[3-[(1-Methylethyl)amino]-2-pyridinyl]-1-piperazinyl]carbonyl]-1H-indol-5-yl]methanesulfonamide; BHAP-U 90152; U-90152. Grades: Highly Purified. CAS No. 136817-59-9. Pack Sizes: 5mg, 10mg, 25mg, 50mg, 100mg. Molecular Formula: C22H28N6O3S. US Biological Life Sciences.
Worldwide
Delavirdine mesylate
Delavirdine is a non-nucleoside reverse transcriptase inhibitor (NNRTI). It is used as part of highly active antiretroviral therapy (HAART) for the treatment of human immunodeficiency virus (HIV) type 1. Uses: Anti-hiv agents. Synonyms: Delavirdine mesylate; Rescriptor; U-90152S; U 90152S; U90152S; U 90152T U-90152T; U90152T; U 90152E; U-90152E; U90152E. Grades: >98%. CAS No. 147221-93-0. Molecular formula: C23H32N6O6S2. Mole weight: 552.67.
Delavirdine mesylate
Delavirdine mesylate. Group: Biochemicals. Alternative Names: N-[2-[[4-[3-[(1-Methylethyl)amino]-2-pyridinyl]-1-piperazinyl]carbonyl]-1H-indol-5-yl]methanesulfonamide methanesulfonate; U-90152S. Grades: Highly Purified. CAS No. 147221-93-0. Pack Sizes: 5mg, 10mg, 25mg, 50mg, 100mg. Molecular Formula: C23H32N6O6S2. US Biological Life Sciences.
Delavirdine (U 90152) mesylate is a potent, highly specific and orally active non-nucleoside reverse transcriptase inhibitor (NNRTI). Delavirdine mesylate selectively inhibits HIV-1 reverse transcriptase (RT) ( IC 50=0.26 μM) over DNA polymerase α (IC 50=440 μM) and polymerase δ (IC 50 >550 μM). Delavirdine mesylate is an inhibitor of HIV-1 replication and can can be used for the study of AIDs [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: U 90152 mesylate; BHAP-U 90152 mesylate. CAS No. 147221-93-0. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg; 200 mg. Product ID: HY-10571A.
Delavirdine, Mesylate (U-90152S)
A bisheteroaryl piperazine (BHAP) reverse transcriptase inhibitor. Group: Biochemicals. Alternative Names: U-90152S. Grades: Highly Purified. Pack Sizes: 10mg. US Biological Life Sciences.
Worldwide
Delavirdine (U-90152)
A bisheteroaryl piperazine (BHAP) reverse transcriptase inhibitor. Group: Biochemicals. Alternative Names: U-90152. Grades: Highly Purified. Pack Sizes: 10mg. US Biological Life Sciences.
Worldwide
Deleobuvir
Deleobuvir, also known as BI207127, a non-nucleoside hepatitis C virus NS5B polymerase inhibitor for the treatment of hepatitis C. Deleobuvir was tested in combination regimens with pegylated interferon and ribavirin, and in interferon-free regimens with other direct-acting antiviral agents including faldaprevir. Deleobuvir showed that a triple combination of deleobuvir, faldaprevir, and ribavirin performed well in HCV genotype 1b patients. Efficacy fell below 50%, however, for dual regimens without ribavirin and for genotype 1a patients. In December 2013, deleobuvir was discontinued since recent findings from phase III trials did not suggest sufficient efficacy. Uses: Designed for use in research and industrial production. Additional or Alternative Names: BI207127; BI-207127; BI 207127; Deleobuvir; BI-207127NA; BI-207127Na. Product Category: Inhibitors. Appearance: Solid powder. CAS No. 863884-77-9. Molecular formula: C34H33BrN6O3. Mole weight: 653.58. Purity: >98%. IUPACName: (E)-3-(2-(1-(2-(5-bromopyrimidin-2-yl)-3-cyclopentyl-1-methyl-1H-indole-6-carboxamido)cyclobutyl)-1-methyl-1H-benzo[d]imidazol-6-yl)acrylic acid. Canonical SMILES: O=C(O)/C=C/C1=CC=C2N=C(C3(NC(C4=CC5=C(C=C4)C(C6CCCC6)=C(C7=NC=C(Br)C=N7)N5C)=O)CCC3)N(C)C2=C1. Product ID: ACM863884779. Alfa Chemistry ISO 9001:2015 Certified.
Deleobuvir
Deleobuvir (BI 207127) is a potent non-nucleoside hepatitis C virus (HCV) NS5B polymerase inhibitor. Uses: Scientific research. Group: Signaling pathways. Alternative Names: BI 207127. CAS No. 863884-77-9. Pack Sizes: 1 mg. Product ID: HY-12634.
Delgocitinib
Delgocitinib, also known as LEO-124249 and JTE052, is a potent and selective JAK inhibitor. JTE-052 reduces skin inflammation and ameliorates chronic dermatitis in rodent models: Comparison with conventional therapeutic agents. JTE-052 regulates contact hypersensitivity by downmodulating T cell activation and differentiation. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Delgocitinib; LEO-124249; LEO124249; LEO 124249; JTE-052; JTE 052; JTE052. Product Category: Inhibitors. Appearance: Solid powder. CAS No. 1263774-59-9. Molecular formula: C16H18N6O. Mole weight: 310.36. Purity: >98%. IUPACName: 3-[(3S,4R)-3-methyl-6-(7H-pyrrolo[2,3-d]pyrimidin-4-yl)-1,6-diazaspiro[3.4]octan-1-yl]-3-oxopropanenitrile. Canonical SMILES: N#CCC(N1C[C@H](C)[C@]12CN(C3=C4C(NC=C4)=NC=N3)CC2)=O. Product ID: ACM1263774599. Alfa Chemistry ISO 9001:2015 Certified.
Delgocitinib
Delgocitinib (JTE-052) is a specific JAK inhibitor with IC 50 s of 2.8, 2.6, 13 and 58 nM for JAK1, JAK2, JAK3 and Tyk2, respectively [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: JTE-052. CAS No. 1263774-59-9. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-109053.
Delmadinone
Delmadinone. Group: Biochemicals. Alternative Names: 6-Chloro-17-hydroxypregna-1,4,6-triene-3,20-dione; Δ1-Chlormadinone. Grades: Highly Purified. CAS No. 15262-77-8. Pack Sizes: 5mg, 10mg, 25mg, 50mg, 100mg. Molecular Formula: C21H25ClO3. US Biological Life Sciences.
Worldwide
Delmadinone Acetate
Progesterone with antiestrogen and antiandrogen activity. Group: Biochemicals. Alternative Names: 17-(Acetyloxy)-6-chloropregna-1,4,6-triene-3,20-dione; 17-Acetoxy-6-chloropregna-1,4,6-triene-3,20-dione; 17α-Acetoxy-6-chloropregna-1,4,6-triene-3,20-dione; 6-Chloro-17-hydroxypregna-1,4,6-triene-3,20-dione Acetate; Delminal; Estrex; RS 1301; Tardastrex; Tarden; Zenadrex; Δ1-Chlormadinone Acetate. Grades: Highly Purified. CAS No. 13698-49-2. Pack Sizes: 5mg. US Biological Life Sciences.
Worldwide
Delmitide
Delmitide is a TNF-alpha production inhibitor potentially for the treatment of Crohn's disease and ulcerative colitis. Synonyms: Allotrap 1258; RDP 58. Grades: >98%. CAS No. 287096-87-1. Molecular formula: C59H105N17O11. Mole weight: 1228.59.
Delmopinol
Delmopinol. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Delmopinol;(+-)-3-(4-Propylheptyl)-4-morpholineethanol;Decapinol;(Rs)-2-(3-(4-propylheptyl)morpholino)ethanol;4-Morpholineethanol, 3-(4-propylheptyl)-, ( -)-;Decapinolum;Delmopinolum;Delmopinolum [inn-latin]. CAS No. 79874-76-3. Molecular formula: C16H33NO2. Mole weight: 0. Purity: 95%+. IUPACName: 2-[3-(4-propylheptyl)morpholin-4-yl]ethanol. Canonical SMILES: CCCC(CCC)CCCC1COCCN1CCO. Density: 0.924g/cm³. Product ID: ACM79874763. Alfa Chemistry ISO 9001:2015 Certified.
Delorazepam
Delorazepam. Group: Biochemicals. Alternative Names: 7-Chloro-5-(2-chlorophenyl)-1,3-dihydro-2H-1,4-benzodiazepin-2-one; 2'-Chloronordiazepam; 7-Chloro-5-(2-chlorophenyl)-3H-1,4-benzodiazepin-2(1H)-one. Grades: Highly Purified. CAS No. 2894-67-9. Pack Sizes: 10mg, 25mg, 50mg, 100mg, 250mg. Molecular Formula: C15H10Cl2N2O. US Biological Life Sciences.
Worldwide
Delpacibart
Delpacibart is a humanized IgG1κ antibody targeting TFRC. TFRC is the most important membrane protein that regulates intracellular iron transport processes [1]. Uses: Scientific research. Group: Inhibitory antibodies. CAS No. 2653183-66-3. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P990051.
Delpazolid
Delpazolid is a novel oxazolidinone antibiotic agent which can inhibit the growth of MSSA and MRSA with a MIC 90 of 2 μg/mL for both of them. Uses: Scientific research. Group: Signaling pathways. Alternative Names: LCB01-0371. CAS No. 1219707-39-7. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-100180.