编号 | 化学名称 | Cas号 | 纯度 | 化学结构 |
---|---|---|---|---|
20624 | Pitolisant HCl | 903576-44-3 | 98% Min. | |
Pitolisant, also known as Tiprolisant, BF2649 and Ciproxidine, is a histamine recepto | ||||
20618 | Pirtobrutinib | 2101700-15-4 | 98% Min. | |
20613 | PLX8394 | 1393466-87-9 | 98% Min. | |
PLX8394 is an orally bioavailable inhibitor of serine/threonine-protein kinase B-raf | ||||
20593 | 吡咯-3-甲醛 | 7126 -39-8 | 98% Min. | |
231106 | PDS-0330 | 2904682-19-3 | ≧98.0% | |
PDS-0330 是一种特异性、有效的Claudin-1抑制剂。PDS-0330 干扰 claudin-1 | ||||
20548 | Pimicotinib | 2253123-16-7 | ≧98.0% | |
Pimicotinib是一种新型的 CSF-1R 小分子抑制剂,可口服、高选择性、 | ||||
20527 | PF-9363 | 98% Min. | ||
20511 | PDD4091 | 1373651-41-2 | ≧98.0% | |
PDD4091 是一种新颖的G6PD抑制剂。 | ||||
20500 | PD089828 | 179343-17-0 | 98% Min. | |
PD089828 is a potent FGFR inhibitor, which inhibits human full-length fibroblast grow | ||||
20499 | PD-173955 | 260415-63-2 | 98% Min. | |
PD-173955 is a src tyrosine kinase inhibitor. PD173955 inhibited Bcr-Abl-dependent ce | ||||
20481 | 6-环丙基-1H-嘧啶-4-酮 | 7038-75-7 | 98% Min. | |
20468 | PD-173212 | 217171-01-2 | 98% Min. | |
PD-173212 is a small molecule N-type calcium channel blocker. PD173212 fully reduced | ||||
20432 | 2-Pyridinamine, 3-(difluoromethoxy)-5-[2-(3,3-difluoro-1-pyrrolidinyl)-6-(1S,4S)-2-oxa-5-azabicyclo[2.2.1]hept-5-yl-4-pyrimidinyl]- | 1637394-01-4 | 98% Min. | |
171458 | Pyrido[2,3-d]pyrimidin-2(1H)-one, 1-[2-cyclobutyl-6-(methylsulfonyl)phenyl]-4-[(2S,5R)-2,5-dimethyl-4-(1-oxo-2-propen-1-yl)-1-piperazinyl]-6-fluoro-7-(2-fluoro-6-hydroxyphenyl)- | 2670380-82-0 | 98% Min. | |
171457 | 2-Pyridinecarboxylic acid, 4,5,6-trichloro-, methyl ester | 496849-76-4 | 98% Min. | |
20399 | 5-(1-propyloxy)-pyrrolidin-2-one | 111712-03-9 | 98% Min. | |
G20374 | (S)-2-甲基-5-氧代哌嗪-1-甲酸叔丁酯 | 1627749-02-3 | 98% Min. | |
20367 | Piflufolastat | 1423758-00-2 | ≧96% | |
Piflufolastat, also known as DCFPYL is a PSMA-targeted PET imaging agent for prostate | ||||
L20351 | PFM01 | 1558598-41-6 | 98% Min. | |
PFM01 is a nuclease-specific MRE11 inhibitor. PFM01 targets MRE11 at a site near the | ||||
L20349 | Poloxin | 321688-88-4 | 98% Min. | |
Poloxin is the first small-molecule inhibitor specifically targeting the function of | ||||
L20345 | Prexasertib free base | 1234015-52-1 | 98% Min. | |
Prexasertib, also know LY2606368, is a n inhibitor of checkpoint kinase 1 (chk1) with | ||||
L20333 | Parsaclisib HCl | 1995889-48-9 | 98% Min. | |
Parsaclisib, also known as INCB050465, is a novel PI3Kδ inhibitor which synergizes w | ||||
L20332 | Parsaclisib free base | 1426698-88-5 | 98% Min. | |
Parsaclisib, also known as INCB050465, is a novel PI3Kδ inhibitor which synergizes w | ||||
20294 | Paltusotine ( CRN-00808 ) | 2172870-89-0 | ≧98.0% | |
Paltusotine 是一类新型的、口服、选择性、非肽类2型生长抑素受体 | ||||
20282 | PS210 | 1221962-86-2 | 98% Min. | |
PS210 is a substrate-selective inhibitor of protein kinase PDK1. It acts by binding t | ||||
20278 | PD-159206 | 171744-42-6 | ≧94.0% | |
PD-159206 is a nucleocapsid inhibitor. It exhibits good antiviral activity against HI | ||||
21251 | PF-06882961 | 2230198-02-2 | 98% Min. | |
PF-06882961 is a potent, orally bioavailable agonist of the glucagon-like peptide-1 r | ||||
21227 | 3PO | 18550-98-6 | 98% Min. | |
3PO is a PFKFB3 (6-phosphofructo-2-kinase/fructose-2,6-bisphosphatase) inhibitor. 3PO | ||||
2073108 | PF-06802861 ( ARRY 371797 ; ARRY-797 ) | 1034189-82-6 | ≧98.0% | |
ARRY 797(也称为ARRY 371797或PF 06802861)是一种具有口服活性,选择性 | ||||
2071623 | PF-04745637 | 1917294-46-2 | 98% Min. | |
PF-04745637 is a TRPV1 antagonist. |