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T70101EMD-66684；化合物 EMD-66684EMD-66684
EMD-66684 is a non-peptide angiotensin II receptor antagonist.
价 格：￥电议型 号：T70101产 地：中国大陆
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T70068AT-1015 hydrochloride monohydrate；化合物 AT-1015 hydrochloride monohydrateAT-1015 hydrochloride monohyd
AT-1015 hydrochloride monohydrate is a serotonin (5-HT)2 receptor antagonist that blocks vascular and platelet 5-HT2A receptors.
价 格：￥电议型 号：T70068产 地：中国大陆
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T70055CO-101244 Free Base；化合物 CO-101244 Free BaseCO-101244 Free Base
CO-101244 Free Base is an NMDA receptor NR2B subunit blocker.
价 格：￥电议型 号：T70055产 地：中国大陆
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T6S1917Schisandrol B；五味子醇乙Gomisin A|||TJN-101|||Besigomsin|||Gamma-Schisandrin|||Schizandrol B|||Wuweizi al
1. Schisandrol B (Besigomsin) may exert neuroprotective effects by attenuating the microglia-mediated neuroinflammatory response via inhibiting the TLR4-mediated NF-κB and MAPKs signaling pathways. 2. Schisandrol B has anti-inflammatory property, potentially result from the inhibition of COX-2, iNOS, IL-6, TNF-α and NO through the down-regulation of RIP2 and NF-κB activation. 3. Schisandrol B induces marked protective effects against hepatic and renal injury induced by CCl(4) exposure through di
价 格：￥电议型 号：T6S1917产 地：中国大陆
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T6S1101Astragalin；紫云英苷Kaempferol 3-D-glucoside|||Kaempferol 3-O-glucoside|||kaempferol-3-glucoside|||3-Gluc
Astragalin (Kaempferol 3-O-glucoside) is a biologically active natural flavonoid. It has a variety of pharmacological properties, including antioxidant, anti-inflammatory, anti-cancer, neuroprotective, and cardioprotective properties.
价 格：￥电议型 号：T6S1101产 地：中国大陆
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T6S1010Allomatrine别苦参碱槐定碱|||别苦参碱
Allomatrine is a natural product from Sophora alopecuroides L. Allomatrine, when given i.c.v., may stimulate the descending dynorphinergic neuron, resulting in the stimulation of KORs in the spinal cord.
价 格：￥电议型 号：T6S1010产 地：中国大陆
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T69912AS2541019；化合物 AS2541019AS2541019
AS2541019 is a selective Phosphatidylinositol-3-kinase p110δ (PI3Kδ) inhibitor.
价 格：￥电议型 号：T69912产 地：中国大陆
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T69732LEI 101 hydrochloride；化合物 LEI 101 hydrochlorideLEI 101 hydrochloride
LEI 101 hydrochloride is potent and selective CB2 partial agonist.
价 格：￥电议型 号：T69732产 地：中国大陆
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T6962Rasagiline Mesylate；甲磺酸雷沙吉兰TVP1012|||AGN1135|||Azilect；TVP1012|||甲磺酸雷沙吉兰|||AGN1135|||Azilect
Rasagiline Mesylate (AGN1135) is a novel MAO-B inhibitor, which can treat idiopathic Parkinson´s disease.
价 格：￥电议型 号：T6962产 地：中国大陆
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T69515R 101933；化合物 R 101933R 101933
R 101933 is a P-glycoprotein (P-gp) inhibitor.
价 格：￥电议型 号：T69515产 地：中国大陆
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T69496MCC1019；化合物 MCC1019MCC1019
MCC1019 is a novel selective inhibitor of the Polo-box domain of Polo-like kinase 1 (PLK1).
价 格：￥电议型 号：T69496产 地：中国大陆
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T69358S101；化合物 S101S101
S101 is an inhibitor of proliferating T-cells, rescuing mice from superantigen-induced shock.
价 格：￥电议型 号：T69358产 地：中国大陆
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T69101NSD-1034；化合物 NSD-1034NSD-1034
NSD-1034 is an amino acid decarboxylase inhibitor.
价 格：￥电议型 号：T69101产 地：中国大陆
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T68973EVT-101 free base；化合物 EVT-101 free baseEVT-101 free base
EVT-101, also known as ENS-101, is an experimental medication which originated from Roche and is under development by Evotec AG for the treatment of major depressive disorder. It acts as a selective NMDA receptor subunit 2B (NR2B) antagonist.
价 格：￥电议型 号：T68973产 地：中国大陆
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T68934VT101 free base；化合物 VT101 free baseVT101 free base
VT101 is a TEAD Auto-palmitoylation inhibitor that Selectively Inhibit Proliferation and Tumor Growth of NF2-deficient Mesothelioma. VT101 inhibited the firefly luciferase reporter dose-dependently and had no 204 effect on the Renilla luciferase reporter.
价 格：￥电议型 号：T68934产 地：中国大陆
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T6891MK-4101；化合物MK4101MK-4101
MK-4101, an effective inhibitor of the Hedgehog pathway, has anti-tumor activity through the induction of extensive apoptosis and inhibition of proliferation in tumor cells.
价 格：￥电议型 号：T6891产 地：中国大陆
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T6880Larotrectinib sulfate；化合物Larotrectinib sulfateLOXO-101 sulfate|||Larotrectinib (LOXO-101) sulfate|||
Larotrectinib sulfate (LOXO-101 sulfate) is an oral active and specific ATP-competitive inhibitor of tropomyosin receptor kinases (TRK).
价 格：￥电议型 号：T6880产 地：中国大陆
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T68796Thr101；化合物 Thr101Thr101
Thr101, also known as NOX Inhibitor VII, is a dose-dependent inhibitor of HDAC1, HDAC3, HDAC4, HDAC5, HDAC6, HDAC7, HDAC8, and HDAC9. Thr101 is also a NOX inhibitor.
价 格：￥电议型 号：T68796产 地：中国大陆
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T687813Ac-SL0101；化合物 3Ac-SL01013Ac-SL0101
3Ac-SL0101 is a potent RSK-specific inhibitor. It facilitates the development of RSK inhibitors as anti-cancer chemotherapeutic agents.
价 格：￥电议型 号：T68781产 地：中国大陆
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T68758UNC10112785；化合物 UNC10112785UNC10112785
UNC10112785 is a novel potent inhibitor of CDK8, CDK19, and CDK9 with IC50 at 1.05, 2.67, and 19.9 nM, respectively, causing MYC loss through both transcriptional and posttranslational mechanisms, and suppressing PDAC anchorage-dependent and anchorage-independent growth, inducing the substantial loss of MYC protein in both two-dimensional (2D) and 3D cell cultures.
价 格：￥电议型 号：T68758产 地：中国大陆
