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T10643c-Fms-IN-1；化合物c-Fms-IN-1c-Fms-IN-1
c-Fms-IN-1 is an inhibitor of c-FMS kinase (IC50 = 0.8 nM).
价 格：￥电议型 号：T10643产 地：中国大陆
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T10642c-di-AMP；环二腺苷酸Cyclic diadenylate|||Cyclic-di-AMP；环二腺苷酸|||Cyclic diadenylate|||Cyclic-di-AMP
c-di-AMP (Cyclic diadenylate) is a STING agonist. It binds to the transmembrane protein STING thereby activating the TBK3-IRF3 signaling pathway.
价 格：￥电议型 号：T10642产 地：中国大陆
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T10641C-82；化合物C-82C-82
C-82 is a specific CBP/β-catenin antagonist. It inhibits the binding between β-catenin and CBP and increases the binding between β-catenin and p300.
价 格：￥电议型 号：T10641产 地：中国大陆
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T10640C-11；化合物 T10640C-11
C-11 is a tubulin inhibitor and acts as an ADC cytotoxin with cytotoxicity for carcinoma cell lines.
价 格：￥电议型 号：T10640产 地：中国大陆
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T1064Norepinephrine bitartrate monohydrate；酒石酸去甲肾上腺素Levophed|||Noradrenaline bitartrate monohydrate；酒石酸去甲
Norepinephrine bitartrate monohydrate (Levophed) is a direct alpha-adrenergic receptors stimulator.
价 格：￥电议型 号：T1064产 地：中国大陆
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T10634Bunaftide；丁萘夫汀Bunaphtide|||Meregon|||Bunaftine；Bunaphtide|||Meregon|||Bunaftine
Bunaftide (Bunaphtid) has antiarrhythmic effects and inhibits aconitine-induced ventricular tachycardia.
价 格：￥电议型 号：T10634产 地：中国大陆
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T10631LBucindolol Formate；化合物Bucindolol FormateBucindolol Formate (71119-11-4 Free base)；Bucindolol Formate
Bucindolol Formatel is a blocker of β1-adrenergic receptor. Bucindolol exhibits intrinsic sympathomimetic activity. Bucindolol can be used in the research of heart failure.
价 格：￥电议型 号：T10631L产 地：中国大陆
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T10625L(Rac)-IBT6A hydrochloride (1412418-47-3 free base)；化合物 T10625L(Rac)-IBT6A hydrochloride；(Rac)-IBT6A
(Rac)-IBT6A hydrochloride is a racemate of IBT6A. IBT6A is an impurity of Ibrutinib. IBT6A can be used in the synthesis of IBT6A Ibrutinib dimer and IBT6A adduct. Ibrutinib is a Btk inhibitor (IC50: 0.5 nM).
价 格：￥电议型 号：T10625L产 地：中国大陆
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T10624BT-13；化合物BT-13BT-13
BT-13 is a selective agonist of glial cell line-derived neurotrophic factor (GDNF) receptor RET independently of GFLs. BT-13 promotes neurite growth from sensory neurons in vitro.
价 格：￥电议型 号：T10624产 地：中国大陆
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T10615BRL44385；化合物 T10615BRL44385
BRL44385 is an effective and selective inhibitor of the replication of HSV-1 and HSV2, Epstein-Barr virus (EBV), and varicella-zoster virus (VZV).
价 格：￥电议型 号：T10615产 地：中国大陆
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T10614BRL-42715；化合物 T10614BRL-42715
BRL-42715 is an effective inhibitor of bacterial beta-lactamases.
价 格：￥电议型 号：T10614产 地：中国大陆
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T10613BRL 37344 sodium；化合物 T10613BRL 37344A；BRL 37344A
BRL 37344 sodium is a specific agonist of the β3-adrenergic receptor. The treatment of BRL 37344 sodium significantly lowers the bodyweight of obese mice.
价 格：￥电议型 号：T10613产 地：中国大陆
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T10612Brexpiprazole S-oxide；化合物 T10612DM-3411；DM-3411
Brexpiprazole S-oxide (DM-3411) is a main metabolite of Brexpiprazole. Brexpiprazole is a partial agonist of human 5-HT1A and dopamine receptors (Kis: 0.12 nM and 0.3 nM).
价 格：￥电议型 号：T10612产 地：中国大陆
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T10610Brexpiprazole-d8；化合物 T10610OPC-34712 D8；OPC-34712 D8
Brexpiprazole D8 (OPC-34712 D8) is a deuterium-labeled Brexpiprazole. Brexpiprazole is a partial agonist of human 5-HT1A and dopamine receptors (Ki: 0.12 nM and 0.3 nM).
价 格：￥电议型 号：T10610产 地：中国大陆
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T1061Toltrazuril；妥曲珠利BAY-i 9142|||Toltrazurilo|||Baycox|||Toltrazurilum；BAY-i 9142|||Toltrazurilo|||妥曲珠利|
Toltrazuril (Toltrazurilo), an antiprotozoal agent, has effect on Coccidia parasites.
价 格：￥电议型 号：T1061产 地：中国大陆
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T10608BRD5648；化合物BRD5648(R)-BRD0705；(R)-BRD0705
BRD5648 ((R)-BRD0705) is an inactive (R)-enantiomer of BRD0705. BRD0705 is a GSK3α inhibitor (IC50: 66 nM; Kd: 4.8 μM) and can be used in acute myeloid leukemia (AML) studies.
价 格：￥电议型 号：T10608产 地：中国大陆
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T10605BRD-K98645985；化合物 T10605BRD-K98645985
BRD-K98645985 is a BAF transcriptional repression inhibitor (EC50: ~2.37 μM). It binds ARID1A-specific BAF complexes, potently reverses HIV-1 latency and prevents nucleosomal positioning.
价 格：￥电议型 号：T10605产 地：中国大陆
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T10604BRD-IN-3；化合物 T10604BRD-IN-3
BRD-IN-3 is a highly potent PCAF bromodomain (BRD) inhibitor (IC50: 7 nM). It also exhibits activity against GCN5 and FALZ.
价 格：￥电议型 号：T10604产 地：中国大陆
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T10602LBRD 4354；化合物BRD 4354BRD 4354
BRD 4354 is an inhibitor of HDAC5 and HDAC9. For HDAC5 and HDAC9, the IC50s values are 0.85 and 1.88 μM, respectively.
价 格：￥电议型 号：T10602L产 地：中国大陆
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T10602BRD 4354 ditrifluoroacetate；化合物 T10602BRD 4354 ditrifluoroacetate (315698-07-8 free base)；BRD 4354 d
BRD 4354 (ditrifluoroacetate) is a moderately potent inhibitor of HDAC5 and HDAC9 (IC50s: 0.85 and 1.88 μM).
价 格：￥电议型 号：T10602产 地：中国大陆
