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T4053AST 487；化合物AST 487NVP-AST 487；NVP-AST 487
AST 487 (NVP-AST 487) is a RET kinase inhibitor, inhibiting RET autophosphorylation and activation of downstream effectors. It also can inhibit Flt-3.
价 格：￥电议型 号：T4053产 地：中国大陆
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T40292Opnurasib；化合物OpnurasibNVP-JDQ443|||JDQ-443|||Opnurasib；NVP-JDQ443|||JDQ-443|||Opnurasib
Opnurasib (JDQ-443) is an orally available and selective and potent covalent KRAS G12C inhibitor with antitumor activity for the study of advanced non-small cell lung cancer.
价 格：￥电议型 号：T40292产 地：中国大陆
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T39858NVP-BSK805 trihydrochlorideNVP-BSK805 trihydrochlorideNVP-BSK805 trihydrochloride
NVP-BSK805 trihydrochloride is a potent ATP-competitive inhibitor of JAK2, exhibiting IC50 values of 0.48 nM, 31.63 nM, 18.68 nM, and 10.76 nM against JAK2 JH1, JAK1 JH1, JAK3 JH1, and TYK2 JH1, respectively.
价 格：￥电议型 号：T39858产 地：中国大陆
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T3965Fevipiprant；非维匹仑QAW039|||NVP-QAW039；QAW039|||NVP-QAW039|||非维匹仑
Fevipiprant (NVP-QAW039) is a selective, potent, reversible competitive CRTh2 antagonist.
价 格：￥电议型 号：T3965产 地：中国大陆
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T39481NVP-DPP728 dihydrochloride；NVP-DPP728 dihydrochlorideNVP-DPP728 dihydrochloride；NVP-DPP728 dihydroch
NVP-DPP728 dihydrochloride is a highly potent, selective, and orally active inhibitor of dipeptidyl peptidase IV (DPP-IV), with a binding affinity (K i ) of 11 nM. This compound proves useful for investigating diabetes mellitus in research studies.
价 格：￥电议型 号：T39481产 地：中国大陆
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T39472NVP-CGM097 (stereoisomer)；NVP-CGM097 (stereoisomer)NVP-CGM097 (stereoisomer)|||CGM097 stereoisomer||
NVP-CGM097 (stereoisomer) is a non-bioactive stereoisomer of NVP-CGM097, which is a potent and selective inhibitor of MDM2.
价 格：￥电议型 号：T39472产 地：中国大陆
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T38896VPM peptide；VPM peptideVPM peptide
VPM peptide functions as a protease-cleavable dithiol cross-linker. It is capable of integration into the PEG-diacrylate (PEG-DA) macromer backbone, resulting in the formation of PEG hydrogel.
价 格：￥电议型 号：T38896产 地：中国大陆
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T37086PDDHVPDDHVPDDHV
PDDHV is a resiniferatoxin-type phorboid vanilloid with capsaicin-like selectivity for the cloned rat transient receptor potential cation channel subfamily V member 1 (TRPV1), formerly known as vanilloid receptor 1. It induces Ca2+-uptake by rat dorsal root ganglion neurons with an EC50 value of 70 nM.
价 格：￥电议型 号：T37086产 地：中国大陆
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T3641NVP-BAW2881；化合物BAW2881BAW2881；BAW2881
NVP-BAW2881 (BAW2881) is a potent and selective VEGFR inhibitor (vascular endothelial growth factor receptor tyrosine kinase inhibitor) with activity to inhibit chronic and acute skin inflammation.
价 格：￥电议型 号：T3641产 地：中国大陆
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T36011p38 MAP Kinase Inhibitor IV；p38 MAPK Inhibitor IVp38 MAPK Inhibitor IV；p38 MAPK Inhibitor IV
p38 MAPK inhibitor IV is an ATP-competitive inhibitor of p38 MAP kinases with IC50 values of 0.13, 0.55, 5.47, and 8.63 μM for p38α, p38β, p38x, and p38δ, respectively, in vitro.[1] It also inhibits LPS-induced TNF-α and IL-1β cytokine production (IC50s = 22 and 44 nM, respectively) in human peripheral blood mononuclear cells.
价 格：￥电议型 号：T36011产 地：中国大陆
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T35071VPC32179；化合物 T35071VPC 32179|||VPC-32179；VPC 32179|||VPC-32179
VPC32179 is a bioactive chemical.
价 格：￥电议型 号：T35071产 地：中国大陆
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T3463NVP-ACC789；化合物NVP-ACC789ACC-789|||ZK202650；ACC-789|||ZK202650
ACC-789 (NVP-ACC789 (ZK202650); ZK-202650) is an effective, specific and orally active inhibitor of the VEGF receptor tyrosine kinases.
价 格：￥电议型 号：T3463产 地：中国大陆
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T33763NVP CXCR2 20；化合物 T33763NVP-CXCR2 20|||NVP CXCR2-20|||NVP CXCR220；NVP-CXCR2 20|||NVP CXCR2-20|||NVP C
NVP CXCR2 20 is an effective selective CXCR2 antagonist (IC50 = 40 nM) with oral bioavailability.
价 格：￥电议型 号：T33763产 地：中国大陆
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T32612LBX192；化合物 T32612NVP-LBX-192|||LBX-192|||LBX 192|||NVP-LBX192|||NVP-LBX 192；NVP-LBX-192|||LBX-192|||
LBX192( NVP-LBX192) is a liver-targeted glucokinase activator.
价 格：￥电议型 号：T32612产 地：中国大陆
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T3261NVP-TNKS656；化合物NVP-TNKS656TNKS656；TNKS656
NVP-TNKS656 (TNKS656) is a highly potent, selective, and orally active TNKS2 inhibitor.
价 格：￥电议型 号：T3261产 地：中国大陆
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T31733EVP-0015962；化合物 T31733EVP-0015962
EVP-0015962, which is bioavailable orally, is a potent and selective gamma-secretase regulator in vitro and in vivo, detectable in the brain.
价 格：￥电议型 号：T31733产 地：中国大陆
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T3114Povidone iodine；聚乙烯吡咯烷酮碘Betadine|||Povidone-iodine|||Isodine|||PVP iodine|||iodopovidone|||PVP-I；Bet
Povidone iodine (Povidone-iodine) exhibits superior antibacterial properties, effectively targeting both MRSA and MSSA strains with minimum inhibitory concentrations (MICs) of 31.25 mg/L and 7.82 mg/L, respectively.
价 格：￥电议型 号：T3114产 地：中国大陆
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T30215AUY-954 free base；化合物 T30215AUY 954|||NVP-AUY954|||AUY-954|||AUY954；AUY 954|||NVP-AUY954|||AUY-954||
AUY-954 is an effective selective S1P(1) modulator. It can significantly reduce the local expression of EAN rat sciatic nerve T cells, B cells, macrophage infiltration, inflammatory demyelination, interleukin-17 and matrix metalloproteinase-9.
价 格：￥电议型 号：T30215产 地：中国大陆
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T29112VPC171；(2-氨基-4-(3-(三氟甲基)苯基)噻吩-3-基)(苯基)甲酮VPC 171|||VPC-171；(2-氨基-4-(3-(三氟甲基)苯基)噻吩-3-基)(苯基)甲酮|||VPC 17
VPC171 is a novel adenosine A1 receptor positive allosteric modulator (PAM).
价 格：￥电议型 号：T29112产 地：中国大陆
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T29111VPC-13566；化合物VPC-13566VPC-13566
VPC-13566 is a BF3-specific small molecule, which effectively inhibited the androgen receptor transcriptional activity and displaced the BAG1L peptide from the BF3 pocket. VPC-13566 inhibits the growth of various prostate cancer cell lines and reduces the growth of AR-dependent prostate cancer xenograft tumors in mice.
价 格：￥电议型 号：T29111产 地：中国大陆
