| RH131542 |
JP1302 |
JP1302 is a potent, selective, high affinity antagonist of the α2C-adrenoceptor,
|
| RH131543 |
JP1302 dihydrochloride |
JP1302 dihydrochloride is a potent, selective, high affinity antagonist of the α
|
| RH131544 |
Y11 |
Y11 inhibits FAK1 autophosphorylation by blocking phosphorylation of Y397 and de
|
| RH131545 |
3-亚环己基-1,3-二氢-2H-吲哚-2-酮 |
3-Cyclohexylidene-1,3-dihydro-2H-indol-2-one
|
| RH131546 |
Raf inhibitor 2 |
Raf inhibitor 2 is a potent raf kinase (IC50<1.0 μM) inhibitor, compound 32,
|
| RH131547 |
DC260126 |
DC260126 is a potent antagonist of GPR40 (FFAR1). DC260126 dose-dependently inhi
|
| RH131548 |
2,3-Diphenylquinoxaline-6-carboxylic acid |
2,3-Diphenylquinoxaline-6-carboxylic acid is used for end-capping in the synthes
|
| RH131549 |
NLRP3/AIM2-IN-2 |
NLRP3/aim2-in-2 (compound 8) is a new potent inhibitor with different species-sp
|
| RH131550 |
CID 60168009 |
CID 60168009
|
| RH131551 |
3-苯基-2-硫代-2,3-二氢-4(1H)-喹唑啉酮 |
3-PHENYL-2-THIOXO-1,2,3,4-TETRAHYDROQUINAZOLIN-4-ONE
|
| RH131552 |
WAY-313356 |
WAY-313356
|
| RH131553 |
1-Cinnamoylpyrrolidine |
1-Cinnamoylpyrrolidine (Compound 3), a crude extract prepared from Piper caninum
|
| RH131554 |
Tyrosinase-IN-2 |
Tyrosinase-IN-2 (compound 67) is a potent inhibitor of tyrosinase. Tyrosinase is
|
| RH131555 |
Resorcinolnaphthalein |
Resorcinolnaphthalein is a specific angiotensin-converting enzyme 2 (ACE2)
|
| RH131556 |
4-(N-(1,8-萘酰亚胺))-N-丁酸 |
Virstatin inhibits the pili system synthesis and prevents A. baumannii biofilm f
|
| RH131557 |
Hepln-13 |
Hepln-13 is a potent and orally active Hepsin inhibitor with an IC50 of 0.33 µM.
|
| RH131558 |
硫酸盐离子载体I |
sulfate-ionophore i
|
| RH131559 |
NSC756093 |
NSC756093
|
| RH131560 |
M-31850 |
M-31850 is a potent, selective and competitive β-hexosaminidase (Hex) inhibitor
|
| RH131561 |
FQ |
FQ is a tyrosinase inhibitor that effectively inhibits the diphenolase activity
|
| RH131562 |
Difluorinated Curcumin(3,4-Difluorobenzylidene curcumin) |
Difluorinated Curcumin (3,4-Difluorobenzylidene curcumin) is a fluorinated curcu
|
| RH131563 |
Zoldonrasib(RMC-9805; KRAS G12D inhibitor 18) |
RMC-9805 (KRAS G12D inhibitor 18) is a potent and orally active KRAS G12D inhibi
|
| RH131564 |
Z-LEED-FMK |
Z-LEED-FMK is a caspase-13 and caspase-4 inhibitor. Z-LEED-FMK also inhibits cas
|
| RH131565 |
Z-LEVD-FMK |
Z-LEVD-FMK is a cell-permeable caspase-4 inhibitor. Z-LEVD-FMK blocks ER stress-
|
| RH131566 |
Z-LEHD-FMK |
Z-LEHD-FMK is a selective and irreversible inhibitor of caspase-9, protects agai
|