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Chemical Structure Cat. No. Product Name CAS No.
2-Bromo-5-fluorothiazole Chemical Structure
BCP19804 2-Bromo-5-fluorothiazole 1209458-83-2
3-[(4-Fluorobenzyl)oxy]benzaldehyde Chemical Structure
BCP20760 3-[(4-Fluorobenzyl)oxy]benzaldehyde 168084-96-6
Intermediate of  PF06463922 Chemical Structure
BCP18904 Intermediate of PF06463922 1454852-76-6
1-Phenyl-1,3,8-triazaspiro[4.5]decan-4-one Chemical Structure
BCP20803 1-Phenyl-1,3,8-triazaspiro[4.5]decan-4-one 1021-25-6
Brivaracetam intermediate 3 Chemical Structure
BCP20788 Brivaracetam intermediate 3 2052297-74-0
(1R,2R)-1-amino-4,4-dimethyl-1,2,3,4-tetrahydronaphthalen-2-ol Chemical Structure
BCP20832 (1R,2R)-1-amino-4,4-dimethyl-1,2,3,4-tetrahydronaphthalen-2-ol 1610347-46-0
Brassinin Chemical Structure
BCP33962 Brassinin 105748-59-2
Brassinin is found in brassicas.
Phosphorus Nitride Chemical Structure
BCP05579 Phosphorus Nitride 61361-50-0
2-Ethynylbenzaldehyde Chemical Structure
BCP33961 2-Ethynylbenzaldehyde 38846-64-9
2'-Bromobiphenyl-2-amine Chemical Structure
BCP33960 2'-Bromobiphenyl-2-amine 54147-91-0
LY-2795050 Chemical Structure
BCP33958 LY-2795050 1346133-08-1
LY2795050 is a nobel kappa opioid receptor selective antagonist.
DTP3 Chemical Structure
BCP23603 DTP3 1809784-29-9
DTP3 is an inhibitor of GADD45β/MKK7 complex.
SEN177 Chemical Structure
BCP33954 SEN177 2117405-13-5
SEN177 is a Glutaminyl cyclase (QPCT) inhibitor.
BD 1047 Chemical Structure
BCP33959 BD 1047 138356-20-4
BD-1047 is a selective functional antagonist of sigma-1 receptor, shows antipsychotic activity in animal models predictive of efficacy in schizophrenia.
EIDD-1931 Chemical Structure
BCP33953 EIDD-1931 3258-02-4
Beta-d-N4-hydroxycytidine is a very potent anti-VEEV (venezuelan equine encephalitis virus) agent with EC50, EC90, and EC99 are 0.426, 1.036, and 2.5 μM, respectively.
ASP7663 Chemical Structure
BCP33952 ASP7663 1190217-35-6
ASP7663 has been found to be a TRPA1 activator and could show abdominal analgesic activities.
SC-43 Chemical Structure
BCP33951 SC-43 1400989-25-4
SC-43 is an agonist of Src-homology protein tyrosine phosphatase-1 (SHP-1) that inactivates STAT3 and reduces liver fibrosis.
2-Benzo[d]thiazolamine,6-[(6,7-dimethoxy-4-quinolinyl)oxy]-5-fluoro- Chemical Structure
BCP33950 2-Benzo[d]thiazolamine,6-[(6,7-dimethoxy-4-quinolinyl)oxy]-5-fluoro- 849217-30-7
Indibulin Chemical Structure
BCP33949 Indibulin 204205-90-3
Indibulin, an orally applicable inhibitor of tubulin assembly, shows potent anticancer activity with a minimal neurotoxicity. Indibulin reduces inter-kinetochoric tension, produces aberrant spindles, activates mitotic checkpoint proteins Mad2 and BubR1, and induces mitotic arrest and apoptosis.
MCHr1 antagonist 2 Chemical Structure
BCP33948 MCHr1 antagonist 2 863115-70-2
MCH-R1 antagonist 22 is a novel potent antagonist of melanin concentrating hormone receptor 1 (MCH-R1).
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