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Chemical Structure Cat. No. Product Name CAS No.
3,4-Diaminofurazan Chemical Structure
BCP00227 3,4-Diaminofurazan 17220-38-1
3,4-Diaminofurazan is a building block used to prepare magnesium and zinc alkynylated salicylaldehyde-diamine Schiff base complexes.
5-Bromo-2-methylbenzoic acid Chemical Structure
BCP08460 5-Bromo-2-methylbenzoic acid 79669-49-1
2-Amino-4-chlorobenzoic acid Chemical Structure
BCP30811 2-Amino-4-chlorobenzoic acid 89-77-0
2-Bromothiazole Chemical Structure
BCP29431 2-Bromothiazole 3034-53-5
2-Bromothiazole is a heterocyclic S compound to induce base-pair substitution and having mutagenic activity.
Ivacaftor Chemical Structure
BCP01857 Ivacaftor 873054-44-5
Ivacaftor is a CFTR activator (IC50 of 43 ± 38 nM).
Ostarine Chemical Structure
BCP02391 Ostarine 841205-47-8
Ostarine (MK-2866) is an androgen receptor modulator (SARM) with an ED50 of 0.44 mg/day.
GS441524 Chemical Structure
BCP35590 GS441524 1191237-69-0
GS-441524 is an adenosine nucleotide analog antiviral, similar to [remdesivir]. This molecule was patented in 2009. In vitro studies of GS-441524 have determined it has a higher EC50 than remdesivir against a number of viruses, meaning GS-441524 is less potent. GS-441524 continues to be studied in the treatment of Feline Infectious Peritonitis Virus, a coronavirus that only infects cats.
5-Methyl-2-(1-methylethoxy)-4-(4-piperidinyl)- benzenamine dihydrochloride Chemical Structure
BCP10607 5-Methyl-2-(1-methylethoxy)-4-(4-piperidinyl)- benzenamine dihydrochloride 1380575-45-0
LCZ696 Chemical Structure
BCP10630 LCZ696 936623-90-4
LCZ696 is a first-in-class dual inhibitor of the angiotensin II receptor(AT II receptor) and neprilysin; a novel single molecule comprising molecular moieties of valsartan and NEP inhibitor prodrug AHU377 .
2-Chloro-4-fluorobenzaldehyde Chemical Structure
BCP29326 2-Chloro-4-fluorobenzaldehyde 84194-36-5
Raltegravir potassium Chemical Structure
BCP01757 Raltegravir potassium 871038-72-1
Raltegravir Potassium Salt is a potent human immunodeficiency virus (HIV) integrase inhibitor
Roxadustat Chemical Structure
BCP02523 Roxadustat 808118-40-3
Roxadustat (FG-4592) is an oral hypoxia-inducible factor (HIF) prolyl hydroxylase inhibitor developed for the treatment of anemia.
2-Bromo-4-fluorobenzaldehyde Chemical Structure
BCP29430 2-Bromo-4-fluorobenzaldehyde 59142-68-6
Alogliptin benzoate Chemical Structure
BCP08885 Alogliptin benzoate 850649-62-6
Alogliptin benzoate is a potent, selective inhibitor of DPP-4 with IC50 of <10 nM, exhibits greater than 10,000-fold selectivity over DPP-8 and DPP-9.
Bilastine Chemical Structure
BCP02576 Bilastine 202189-78-4
Bilastine is a selective histamine H1 receptor antagonist used for treatment of allergic rhinoconjunctivitis and urticaria.
(R)-2-(2,5-difluorophenyl)pyrrolidine hydrochloride Chemical Structure
BCP25200 (R)-2-(2,5-difluorophenyl)pyrrolidine hydrochloride 1218935-60-4
6-Bromo-4-fluoro-1-isopropyl-2-methyl-1H-benzo[d]imidazole Chemical Structure
BCP14302 6-Bromo-4-fluoro-1-isopropyl-2-methyl-1H-benzo[d]imidazole 1231930-33-8
Nicotinamide Riboside Chloride Chemical Structure
BCP20094 Nicotinamide Riboside Chloride 23111-00-4
Nicotinamide riboside is a pyridine-nucleoside form of vitamin B3 that functions as a precursor to nicotinamide adenine dinucleotide or NAD+.
2-Bromo-N,N-dimethylacetamide Chemical Structure
BCP29819 2-Bromo-N,N-dimethylacetamide 5468-77-9
Etravirine Chemical Structure
BCP03562 Etravirine 269055-15-4
Etravirine is a novel HIV reverse transcriptase inhibitor useful in treatment of HIV infection.
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