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T22697CS 2100；化合物CS 21001-[[4-Ethyl-5-[5-(4-phenoxyphenyl)-1,2,4-oxadiazol-3-yl]-2-thienyl]methyl]-3-azeti
CS 2100 (1-[[4-Ethyl-5-[5-(4-phenoxyphenyl)-1,2,4-oxadiazol-3-yl]-2-thienyl]methyl]-3-azetidinecarboxylic acid) is an S1P1 agonist.
价 格：￥电议型 号：T22697产 地：中国大陆
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T21100Dodecanedinitrile；化合物 T211001,10-Decamethylenedinitrile|||Decamethylenedinitrile|||1,12-Dodecanedini
Dodecanedinitrile is a bioactive chemical.
价 格：￥电议型 号：T21100产 地：中国大陆
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T16829(S)-BI-1001；化合物 T16829(S)-BI-1001
(S)-BI-1001 is an active S-enantiomer of BI-1001. (S)-BI-1001 has antiviral potency against HIV-1 integrase (IC50: 28 nM, and EC50: 450 nM and a Kd: 4.7 μM).
价 格：￥电议型 号：T16829产 地：中国大陆
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T15480HG6-64-1；化合物 T15480HMSL 10017-101-1；HMSL 10017-101-1
HG6-64-1 is a potent and selective inhibitor of B-Raf (IC50: 0.09 μM on B-raf V600E transformed Ba/F3 cells).
价 格：￥电议型 号：T15480产 地：中国大陆
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T15166DPM-1001；化合物 T15166DPM-1001
DPM-1001 is an orally bioavailable and non-competitive protein-tyrosine phosphatase (PTP1B) inhibitor (IC50: 100 nM) with the anti-diabetic property.
价 格：￥电议型 号：T15166产 地：中国大陆
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T13294Veledimex (S enantiomer)；化合物 T13294RG-115932 S enantiome|||INXN-1001 S enantiome；RG-115932 S enantio
Veledimex S enantiomer is the S enantiomer of veledimex. Veledimex is an oral activator ligand for a proprietary gene therapy promoter system and CYP3A4/5 inhibitor.
价 格：￥电议型 号：T13294产 地：中国大陆
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T13293LVeledimex；化合物 T13293LRG-115932|||INXN-1001；RG-115932|||INXN-1001
Veledimex is an oral activator ligand for a proprietary gene therapy promoter system. It is also a moderate inhibitor of and substrate for CYP3A4/5.
价 格：￥电议型 号：T13293L产 地：中国大陆
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T13293Veledimex racemate；化合物 T13293RG-115932 racemate|||INXN-1001 racemate；RG-115932 racemate|||INXN-1001
Veledimex racemate, the racemic form of veledimex, is an orally available, small-molecule ligand that activates the RheoSwitch Therapeutic System.
价 格：￥电议型 号：T13293产 地：中国大陆
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T12782RWJ-445167；化合物 T127823DP-10017；3DP-10017
RWJ-445167 is a thrombin and factor Xa dual inhibitor(Ki of 4.0 nM and 230 nM, respectively), with potent antithrombotic activity.
价 格：￥电议型 号：T12782产 地：中国大陆
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T12609R-10015；化合物R-10015R-10015
R-10015 is a highly potent and selective LIMK inhibitor that blocks LIMK by binding to the ATP-binding pocket. It inhibits human LIMK1 with an IC50 value of 38 nM. It also exerts broad-spectrum antiviral effects and may be used in HIV infection research.
价 格：￥电议型 号：T12609产 地：中国大陆
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T11001L1N-Desethyl Chloroquine Hydrochloride；化合物T11001L1(±)-Desethylchloroquine 2HCl；(±)-Desethylchloroquine
N-Desethyl Chloroquine Hydrochloride ((±)-Desethylchloroquine 2HCl) is a desethylchloroquine derivative. desethylchloroquine competitively inhibits cyp2d1 /6-mediated reactions in vitro and in vivo.
价 格：￥电议型 号：T11001L1产 地：中国大陆
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T11001LDesethyl chloroquine diphosphate；化合物 T11001LDesethyl chloroquine diphosphate
Desethyl chloroquine diphosphate is the main deethyl metabolite of chloroquine. Chloroquine diphosphate is an inhibitor of autophagy and toll-like receptors (TLRs). Chloroquine diphosphate has anti-plasma activity.
价 格：￥电议型 号：T11001L产 地：中国大陆
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T11001Desethyl chloroquine；去乙基氯喹Monodesethylchloroquine|||N-deethylchloroquine；Monodesethylchloroquine|||N
Desethyl chloroquine (Monodesethylchloroquine) is a major metabolite of Chloroquine which is a TLR inhibitor. Desethyl chloroquine shows antiplasmodic activity.
价 格：￥电议型 号：T11001产 地：中国大陆
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T10585Bozitinib；化合物BozitinibCBT-101|||PLB-1001；CBT-101|||PLB-1001
Bozitinib (PLB-1001) (PLB-1001) is a highly selective inhibitor of the c-MET kinase with blood-brain barrier permeability. Bozitinib binds to the conventional ATP-binding pocket of the tyrosine kinase superfamily.
价 格：￥电议型 号：T10585产 地：中国大陆
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T10565BMS-1001 hydrochloride；化合物BMS-1001 hydrochlorideBMS-1001 hydrochloride
BMS-1001 hydrochloride is an orally active inhibitor of human PD-1/PD-L1 immune checkpoint with low-toxicity in cells.BMS-1001 alleviates the inhibitory effect of the soluble PD-L1 on the T-cell receptor-mediated activation of T-lymphocytes. BMS-1001 is capable of alleviating the PD-1/PD-L1 immune checkpoint-mediated exhaustion of Jurkat T-lymphocytes.
价 格：￥电议型 号：T10565产 地：中国大陆
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T10462LBavisant dihydrochloride hydrate；化合物 T10462LJNJ31001074AAC；JNJ31001074AAC
Bavisant dihydrochloride hydrate (JNJ31001074AAC) is a highly selective, orally active antagonist of the human H3 receptor with a novel mechanism of action, involving wakefulness and cognition, with potential as a treatment for ADHD. in vivo: Mean change from baseline in the total ADHD-RS-IV score at day 42 (primary efficacy endpoint) was -8.8 in the placebo group versus -9.3, -11.2 and -12.2 in the bavisant 1 mg/day, 3 mg/day and 10 mg/day groups, respectively; the change in the 10 mg/day group
价 格：￥电议型 号：T10462L产 地：中国大陆
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T100191-Methylcytosine1-甲基胞嘧啶1-methylcytosin|||4-amino-1-methylpyrimidin-2(1H)-one|||1-甲基胞嘧啶|||N-Methylcyt
1-Methylcytosine (4-amino-1-methylpyrimidin-2(1H)-one) is a methylated form of the cytosine and can be used as the nucleobase of hachimoji DNA paired with isoguanine.
价 格：￥电议型 号：T10019产 地：中国大陆
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T100171-Linoleoyl Glycerol一亚油酸甘油酯Glycerol 1-monolinolate|||Monolinolein|||一亚油酸甘油酯|||Glyceryl monolinoleate
1-Linoleoyl Glycerol (Monolinolein) is fatty acid glycerol that has been isolated from Saururus Chinensis roots. The (R)-1-Linoleoyl Glycerol and (S)-1-Linoleoyl Glycerol exhibit Lipoprotein-associated phospholipase A2 (Lp-PLA2) inhibitory activities with IC50 values of 45.0 and 52.0 μM, respectively.
价 格：￥电议型 号：T10017产 地：中国大陆
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T100151-Deazaadenosine；化合物 T100151-Deazaadenosine
1-Deazaadenosine is a potent Adenosine deaminase inhibitor (Ki: 0.66 μM). It exhibits anti-cancer activities in vitro and has the potential to be a chemotherapy agent for lymphoproliferative disorders.
价 格：￥电议型 号：T10015产 地：中国大陆
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T100131-Acetyl-3-o-toluyl-5-fluorouracil；化合物 T10013A-?OT-?Fu；A-?OT-?Fu
1-Acetyl-3-o-toluyl-5-fluorouracil is a potent antineoplastic agent.
价 格：￥电议型 号：T10013产 地：中国大陆
