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Chemical Structure Cat. No. Product Name CAS No.
DATP-N3 Chemical Structure
BCP46395 DATP-N3 1048021-78-8
Fenquizone Chemical Structure
BCP46379 Fenquizone 20287-37-0
Fenquizone is a member of quinazolines.
TC-FPR 43 Chemical Structure
BCP46377 TC-FPR 43 903895-98-7
TC-FPR 43 is a potent formyl peptide receptor 2 (FPR2) agonist.
GSK2256294A Chemical Structure
BCP46295 GSK2256294A 1142090-23-0
GSK2256294A is a potent and selective sEH inhibitor, which is in investigation in patients with endothelial dysfunction or abnormal tissue repair, such as diabetes, wound healing or COPD. GSK2256294 exhibited potent cell-based activity, a concentration-dependent inhibition of the conversion of 14,15-EET to 14,15-DHET in human, rat and mouse whole blood in vitro, and a dose-dependent increase in the LTX/LTX diol ratio in rat plasma following oral administration.
Cedazuridine Chemical Structure
BCP46046 Cedazuridine 1141397-80-9
Cedazuridine, also known as E 7727 and WHO 10741, is a cytidine deaminase inhibitor. Decitabine/cedazuridine, sold under the brand name Inqovi, is a fixed-dosed combination medication for the treatment of adults with myelodysplastic syndromes (MDS) and chronic myelomonocytic leukemia (CMML). It is a combination of decitabine, a nucleoside metabolic inhibitor, and cedazuridine, a cytidine deaminase inhibitor.
Propylthiouracil Chemical Structure
BCP22165 Propylthiouracil 51-52-5
Propylthiouracil is a Thyroid Hormone Synthesis Inhibitor. The mechanism of action of propylthiouracil is as a Thyroid Hormone Synthesis Inhibitor.
Dov-Val-Dil-OH TFA Chemical Structure
BCP46016 Dov-Val-Dil-OH TFA 133120-90-8
Dov-Val-Dil-OH is a useful chemical intermediate for synthesis of auristatin-related compounds, such as Monomethyl auristatin E (MMAE), Auristatins are antimitotic agents which inhibits cell division by blocking the polymerisation of tubulin.
Fluphenazine enanthate Chemical Structure
BCP45972 Fluphenazine enanthate 2746-81-8
Fluphenazine enanthate is a member of phenothiazines.
BC-1471 Chemical Structure
BCP45967 BC-1471 896683-84-4
BC-1471 is a selective antagonist of deubiquitinase STAM-binding protein (STAMBP) which decreases NALP7 protein levels and suppresses IL-1β release after TLR agonism.
AGI-25696 Chemical Structure
BCP45966 AGI-25696 2201066-35-3
AGI-25696 is a methionine adenosyltransferase 2A (MATA2 ) inhibitors useful for treatment of cancer. AGI-25696 blocks growth of MTAP-deleted tumors in vivo.
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