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T10699L2CBB1007 trihydrochloride (1379573-92-8 free base)；化合物 T10699L2CBB1007 trihydrochloride；CBB1007 trihy
CBB1007 trihydrochloride is a selective, reversible, and substrate competitive LSD1 inhibitor (IC50: 5.27 μM for hLSD1).
价 格：￥电议型 号：T10699L2产 地：中国大陆
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T10699LCBB1007；化合物 T10699LCBB1007
CBB1007 is a potent, reversible, and substrate competitive LSD1 inhibitor (IC50: 5.27 μM for hLSD1).
价 格：￥电议型 号：T10699L产 地：中国大陆
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T10699CBB1007 hydrochloride (1379573-92-8 free base)；化合物 T10699CBB1007 hydrochloride；CBB1007 hydrochloride
CBB1007 Hcl is a selective, reversible, and substrate competitive LSD1 inhibitor (IC50: 5.27 μM for hLSD1).
价 格：￥电议型 号：T10699产 地：中国大陆
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T10698LCBB1003 hydrochloride (1379573-88-2 free base)；化合物 T10698LCBB1003 hydrochloride；CBB1003 hydrochlorid
CBB1003 hydrochloride is a new inhibitor of histone demethylase LSD1 (IC50: 10.54 μM).
价 格：￥电议型 号：T10698L产 地：中国大陆
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T10698CBB1003；化合物 T10698CBB1003
CBB1003 is a new inhibitor of histone demethylase LSD1 (IC50: 10.54 μM).
价 格：￥电议型 号：T10698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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T10282Aliskiren D6 Hydrochloride；化合物 T10282SPP 100 D6 Hydrochloride|||CGP60536B D6 Hydrochloride|||CGP 605
Aliskiren (CGP 60536) D6 Hydrochloride is a deuterium-labeled Aliskiren. Aliskiren hemifumarate is a direct and orally active renin inhibitor (IC50: 1.5 nM).
价 格：￥电议型 号：T10282产 地：中国大陆
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T10252L3ADU-S100；化合物 T10252L3ML RR-S2 CDA|||MIW815；ML RR-S2 CDA|||MIW815
ADU-S100 is an activator of stimulator of interferon genes (STING).
价 格：￥电议型 号：T10252L3产 地：中国大陆
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T10252L2ADU-S100 ammonium salt；化合物ADU-S100 ammonium saltML RR-S2 CDA ammonium salt|||MIW815 ammonium salt；ML
ADU-S100 ammonium salt (ML RR-S2 CDA ammonium salt) is an activator of stimulator of interferon genes (STING). ADU-S100 ammonium salt leads to potent and systemic tumor regression and immunity.
价 格：￥电议型 号：T10252L2产 地：中国大陆
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T10252LADU-S100 enantiomer ammonium salt；化合物 T10252LMIW815 enantiomer ammonium salt|||ML RR-S2 CDA enantiom
ADU-S100 (MIW815) enantiomer ammonium salt is the less active enantiomer of ADU-S100. ADU-S100 is an activator of the stimulator of interferon genes (STING).
价 格：￥电议型 号：T10252L产 地：中国大陆
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T10252ADU-S100 disodium salt；化合物 T10252ML RR-S2 CDA disodium salt|||MIW815 disodium salt；ML RR-S2 CDA diso
ADU-S100 (MIW815) disodium salt is an activator of stimulator of interferon genes (STING).
价 格：￥电议型 号：T10252产 地：中国大陆
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T10223ABT-100；化合物 T10223ABT-100
ABT-100 is a potent, highly selective, and orally active farnesyl transferase inhibitor with broad-spectrum antitumor activity.
价 格：￥电议型 号：T10223产 地：中国大陆
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T10100QF0301B；化合物QF0301BQF0301B
QF0301B is a potent α1-adrenergic receptor antagonist with inhibitory effects on α2-adrenergic receptors, 5-HT2A and histamine H1 receptors.
价 格：￥电议型 号：T10100产 地：中国大陆
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T10098PGS-IN-1；化合物PGS-IN-1KME-4；KME-4
PGS-IN-1 (KME-4) is a potent inhibitor of prostaglandin synthetase (PGS, IC50: 0.28 μM) and 5-lipoxygenase (IC50: 1.05 μM).
价 格：￥电议型 号：T10098产 地：中国大陆
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T10097(2S,3S)-E1R；化合物 T10097(2S,3S)-E1R
(2S,3S)-E1R (Compound 2d) is an enantiomer of E1R. (2R,3R)-E1R is a sigma-1 receptor positive allosteric modulator for the treatment of cognition/memory disorders.
价 格：￥电议型 号：T10097产 地：中国大陆
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T10096L2(2S,3R)-Voruciclib hydrochloride；化合物 T10096L2(2S,3R)-Voruciclib hydrochloride (1253731-24-6 free bas
(2S,3R)-Voruciclib hydrochloride is the (2S,3R)-enantiomer of Voruciclib. It is an orally active CDK inhibitor.
价 格：￥电议型 号：T10096L2产 地：中国大陆
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T10096LVoruciclib；化合物VoruciclibVoruciclib
Voruciclib is an orally active and selective CDK inhibitor (Ki: 0.626 nM-9.1 nM). Voruciclib represses the expression of MCL-1 in multiple models of diffuse large B-cell lymphoma. Voruciclib effectively blocks CDK9, the transcriptional regulator of MCL-1.
价 格：￥电议型 号：T10096L产 地：中国大陆
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T10096(2S,3R)-Voruciclib；化合物 T10096(2S,3R)-Voruciclib
(2S,3R)-Voruciclib is the (2S,3R)-enantiomer of Voruciclib. It is an orally active CDK inhibitor.
价 格：￥电议型 号：T10096产 地：中国大陆
