R21082488 |
Lats-IN-1 |
Lats-in-1 is a potent and ATP-competitive inhibitor of Lats1 and Lats2 kinases.
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R21082489 |
BMS-986177 |
Milvexian, also known as BMS-986177, is a blood coagulation factor XIa inhibitor
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R21082490 |
1808258-86-7 |
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R21082491 |
LSN3346149 |
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R21082492 |
IA-14069 |
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R21082493 |
ASTX-029 |
ASTX029 is a synthetic small molecule inhibitor of extracellular signal-regulate
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R21092501 |
Sulfopin(PIN1-3) |
Sulfopin (PIN1-3) is a highly selective covalent inhibitor of Pin1 wit
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R2109301 |
JTE-607 dihydrochloride |
Antiinfective therapy, Treatment of Septic Shock, Antiinflammatory Drugs, Cytoki
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R2110001 |
AR-C155858 |
AR-C155858 is a selective monocarboxylate transporter MCT1 and MC
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R21101501 |
DZD9008 |
DZD9008是一种设计合理、选择性强、不可逆的EGFR/HER2抑制剂。
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R21102501 |
TPX0131;TPX-0131 |
TPX-0131 is a potent, selective, CNS-penetrant and orally active inhibitor of&nb
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R21111201 |
BDA-366 |
BDA-366 is a Small-Molecule Bcl2 BH4 Antagonist for Lung Cancer Therapy.
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R21111202 |
DL-alpha-Tocopherol |
DL-alpha-Tocopherol is a synthetic vitamin E, with antioxidation effect. DL-alph
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R21111203 |
NVS-PAK1-1 |
NVS-PAK1-1 is a potent and selective allosteric PAK1 inhibitor with an IC50 of 5
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R21111204 |
CP-609754 (OSI754) |
CP-609754 (LNK-754) is a potent and reversible farnesyltransferase inhibitor wit
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R21111205 |
STK16-IN-1 |
STK16-IN-1 is a STK16 kinase inhibitor with an IC50 of 295 nM.
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R21111206 |
Pexidartinib hydrochloride;PLX-3397 HCl |
Pexidartinib hydrochloride (PLX-3397 hydrochloride) is a potent, orally active,
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R21111207 |
UT-155 |
UT-155 is a selective and potent androgen receptor (AR) antagonist, with a Ki of
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R21111208 |
Parsaclisib |
Parsaclisib (INCB050465) is a potent, selective and orally active inhibitor of P
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R21111209 |
Parsaclisib hydrochloride |
Parsaclisib hydrochloride (INCB050465 hydrochloride) is a potent, selective and
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R21111210 |
AZD-0284 |
AZD-0284 is a selective inverse agonist of the nuclear receptor RORγ. AZD-0284 h
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R21111211 |
Lumateperone tosylate |
Lumateperone tosylate (ITI-007 tosylate) is a 5-HT 2A receptor antagonist (KI= 0
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R21111212 |
Encorafenib |
Encorafenib (LGX818) is a highly potent BRAF inhibitor with selective anti-proli
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R21071288 |
Val-Cit-PAB-MMAE |
Val-Cit-PAB-MMAE is a drug-linker conjugate for ADC. Val-Cit-PAB-MMAE conta
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R21111501 |
IMP-1088 |
IMP-1088 is a potent human N-myristoyltransferases NMT1 and NMT2&
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