Home   >  

Classified by application

All Products

Signaling Pathways

Research Areas

Nature products






Raw Materials


Chemical Structure Cat. No. Product Name CAS No.
Sinapic acid Chemical Structure
BCP25316 Sinapic acid 530-59-6
Sinapic acid is found in american cranberry. Sinapic acid is a common constituent of plants and fruit.
RBN-2397 Chemical Structure
BCP33764 RBN-2397 2381037-82-5
RBN-2397 is a potent, accross species and orally active NAD+ competitive inhibitor of PARP7 (IC50<3 nM).
PF-06826647 Chemical Structure
BCP33615 PF-06826647 2127109-84-4
PF-06826647(Tyk2-IN-8) is a selective TYK2 inhibitor, which binds to TYK2 catalytically active JH1 domain with an IC50 of 17 nM, used in the treatment of psoriasis.
Alobresib Chemical Structure
BCP33313 Alobresib 1637771-14-2
Alobresib is an antineoplastic drug candidate.
Phthalazinone pyrazole Chemical Structure
BCP33311 Phthalazinone pyrazole 880487-62-7
Phthalazinone pyrazole is a potent, selective and orally bioavailable inhibitor of Aurora-A kinase.
UNC-926 Hydochloride Chemical Structure
BCP25396 UNC-926 Hydochloride 1782573-49-2
UNC-926 is a methyl-lysine (Kme) reader domain inhibitor; inhibits L3MBTL1 with an IC50 of 3.9 μM.
BETd-260 Chemical Structure
BCP33276 BETd-260 2093388-62-4
BETd-260 is a potent BET degrader based on PROTAC technology, with as low as 30 pM against BRD4 protein in RS4;11 leukemia cell line.
Rucaparib camsylate Chemical Structure
BCP25678 Rucaparib camsylate 1327258-57-0
Rucaparib camsylate is a camphorsulfonate salt obtained by reaction of rucaparib with one molar equivalent of (1S,4R)-camphorsulfonic acid. It is an inhibitor of poly (ADP-ribose) polymerase and is used as monotherapy for advanced ovarian cancer and deleterious germline or somatic BRCA mutation.
CC-90011 besylate Chemical Structure
BCP33218 CC-90011 besylate 2097523-60-7
CC-90011 is a potent and orally active LSD1 inhibitor. CC-90011 binds to and inhibits LSD1, a demethylase that suppresses the expression of target genes by converting the di- and mono-methylated forms of lysine at position 4 of histone H3 (H3K4) to mono- and unmethylated H3K4, respectively.
Valproic acid Chemical Structure
BCP33204 Valproic acid 99-66-1
Valproic acid is an inhibitor of histone deacetylase (HDAC) inhibitor, which has an anticancer effect. Valproic acid was shown to induce proliferation and enhance self-renewal of hematopoietic stem cells (HSC).
123下一页末页共 522 条记录 1 / 53 页