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T12774RSV-IN-1RSV-IN-1
RSV-IN-1 is an inhibitor of human respiratory syncytical virus (hRSV)(IC50 of 0.11 μM).
价 格：￥电议型 号：T12774产 地：美洲
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T12781RV01RV01
RV01 is an analogue of resveratrol. RV01 decreases iNOS expression, with anti-neuroinflammatory activity.
价 格：￥电议型 号：T12781产 地：美洲
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T12783RWJ 50271RWJ 50271
RWJ 50271 is a selective lymphocyte function-associated antigen-1/intercellular adhesion molecule-1(LFA-1/ICAM-1) interaction inhibitor( IC50 of 5.0 μM in HL60 cells).
价 格：￥电议型 号：T12783产 地：美洲
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T13080Taranabant ((1R,2R)stereoisomer)Taranabant ((1R,2R)stereoisomer),MK0364 (1R,2R)stereoisomer,
Taranabant (1R,2R)stereoisomer is the R-enantiomer of Taranabant. Taranabant is a highly potent and selective inverse agonist of cannabinoid 1 (CB1) receptor.
价 格：￥电议型 号：T13080产 地：美洲
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T13194CSF1R-IN-2CSF1R-IN-2
CSF1R-IN-2 is an oral-active SRC, MET and c-FMS inhibitor(IC50 of 0.12 nM, 0.14 nM and 0.76 nM for SRC, MET and c-FMS respectively).
价 格：￥电议型 号：T13194产 地：美洲
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T13423(1R,2R)-2-PCCA(hydrochloride)(1R,2R)-2-PCCA(hydrochloride)
(1R,2R)-2-PCCA hydrochloride is a diastereomer of 2-PCCA, and is a potent agonist of GPR88 receptor(EC50 of 3 nM and 603 nM in cell-free assay and in cell assay).
价 格：￥电议型 号：T13423产 地：美洲
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T13424(1R,2S)-VU0155041(1R,2S)-VU0155041
(1R,2S)-VU0155041 is a partial agonist of mGluR4(EC50 of 2.35 μM).
价 格：￥电议型 号：T13424产 地：美洲
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T13462(+)-DHMEQ(+)-DHMEQ,(1R,2R,6R)-Dehydroxymethylepoxyquinomicin,(1R,2R,6R)-DHMEQ
(+)-DHMEQ is an antioxidant transcription factor Nrf2 activator. (+)-DHMEQ is the enantiomer of (-)-DHMEQ.
价 格：￥电议型 号：T13462产 地：美洲
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T16776RO9021RO9021
RO9021 is an orally bioavailable, novel ATP-competitive SYK inhibitor (average IC50: 5.6 nM).
价 格：￥电议型 号：T16776产 地：美洲
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T17424E1rcat4E1rcat
4E1RCat is a dual inhibitor of eIF4E:eIF4G and eIF4E:4E-BP1 interaction. And it inhibits the binding of eIF4G to eIF4E with IC50 of 3.2 μM.
价 格：￥电议型 号：T1742产 地：美洲
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T2236RU58841RU58841,HMR-3841,PSK-3841
RU 58841 is a specific androgen receptor antagonist or anti-androgen; RU 58841 has a significant effect on hair regrowth.
价 格：￥电议型 号：T2236产 地：美洲
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T2282RPI-1RPI-1,RPI1,RPI 1
RPI-1 is a competitive, potent ATP-dependent Ret kinase inhibitor.?
价 格：￥电议型 号：T2282产 地：美洲
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T5486RU320521RU320521,RU.521,
RU.521 (RU320521) is a potent dsDNA inhibitor (IC50 : 700 nM), inhibition of the dsDNA pathway by RU.521 requires the presence of cGAS.
价 格：￥电议型 号：T5486产 地：美洲
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T8746LI-49 free base；化合物I-49 free basePyrido[4,3-d]pyrimidin-7(6H)-one, 2-methyl-4-[[(1R)-1-[2-methyl-3-(t
I-49 free base (Pyrido[4,3-d]pyrimidin-7(6H)-one, 2-methyl-4-[[(1R)-1-[2-methyl-3-(trifluoromethyl)phenyl]ethyl]amino]-6-(tetrahydro-2H-pyran-4-yl)-) is a novel benzylamino substituted pyridopyrimidinone as SOS1 inhibitor.
价 格：￥电议型 号：T8746L产 地：中国大陆
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T8467RET V804M-IN-1；化合物RET V804M-IN-1RETV804M kinase inhibitor|||LUN09945；RETV804M kinase inhibitor|||LUN
RET V804M-IN-1 (RETV804M kinase inhibitor) is a wt-RET -selective RETV804M kinase inhibitors(IC50 = 20 nM).
价 格：￥电议型 号：T8467产 地：中国大陆
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T8409SYN1143；化合物AMG-1RON-IN-1|||AMG-1；RON-IN-1|||AMG-1
SYN1143 (AMG-1) is a potent inhibitor of human RON and c-Met.In vitro kinase assays showed that compound I is a potent inhibitor of human RON and c-Met with IC50s of 9 and 4 nmol/L, respectively.
价 格：￥电议型 号：T8409产 地：中国大陆
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T83576(1R)-Deruxtecan；化合物 (1R)-Deruxtecan(1R)-Deruxtecan
Deruxtecan (1R) is a drug-linker conjugate for antibody-drug conjugates (ADC) [1].
价 格：￥电议型 号：T83576产 地：中国大陆
