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T11137(E)-GABAB receptor antagonist 1(E) GABAB receptor antagonist 1,(E)GABAB receptor antagonist 1
(E)-GABAB receptor antagonist 1 is a trans-GABAB receptor antagonist 1. (E)-GABAB receptor antagonist 1 decreases GABA-induced IP3 (inositol trisphosphate) production with IC50 of 37.9 μM. GABAB receptor antagonist 1 is a selective and negative allosteric modulator of GABAB (γ-Aminobutyric acid) receptors.
价 格：￥电议型 号：T11137产 地：中国大陆
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T12320ORL1 antagonist 1ORL-1 antagonist 1,ORL1 antagonist 1
ORL1 antagonist 1 is an o antagonist of pioid receptor-like 1 (ORL1) (IC50 of 61 nM).
价 格：￥电议型 号：T12320产 地：中国大陆
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T7053p-Hydroxycinnamic acidInhibitor,Prostaglandin Receptor,p Hydroxycinnamic acid,p-Hydroxycinnamic acid
p-Hydroxycinnamic acid can inhibit platelet activity, with IC50s of 371 μM, 126 μM for thromboxane B2 production and lipopolysaccharide-induced prostaglandin E2 generation, respectively.
价 格：￥电议型 号：T7053产 地：中国大陆
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T11077Dopamine D2 receptor antagonist-1Dopamine D-2 receptor antagonist-1,Dopamine D2 receptor antagonist
Dopamine D2 receptor antagonist-1 is a negative allosteric modulator (NAM) of dopamine D2 receptor (D2R), with sub-mM affinity.
价 格：￥电议型 号：T11077产 地：中国大陆
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T9983CCR8 antagonist 1
CCR8 antagonist 1 is an antagonist of C-C Motif Chemokine Receptor 8 (CCR8) with a Ki value of 1.6 nM.
价 格：￥电议型 号：T9983产 地：中国大陆
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T2S0765Epibetulinic acidNO Synthase,Nitric oxide synthases,Prostaglandin Receptor,NOS,inhibit,Inhibitor,Epi
Epibetulinic acid has anti-inflammatory activity, it exhibits potent inhibitory effects on NO and prostaglandin E(2) production in mouse macrophages (RAW 264.7) stimulated with bacterial endotoxin.
价 格：￥电议型 号：T2S0765产 地：中国大陆
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T67733BT44RETagonistBT44
BT44 is a novel, second-generation glial cell linederived neurotropic factor mimetic with improved biological activity and is a lead compound for the treatment of neurodegenerative disorders.
价 格：￥电议型 号：T67733产 地：中国大陆
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TQ0290ONO-AE3-208ONOAE3208,ONO AE3 208,Prostaglandin Receptor,inhibit,ONO-AE-3-208,Inhibitor
ONO-AE3-208 is an EP4 antagonist. It suppresses cell migration, invasion, and metastasis of prostate cancer.
价 格：￥电议型 号：TQ0290产 地：中国大陆
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T125975-HT2 antagonist 15HT2 antagonist 1,5 HT2 antagonist 1,5-HT-2 antagonist 1
5-HT2 antagonist 1 is a potent 5-HT2 receptor antagonist, has weak α1 adrenoceptor blocking activity.
价 格：￥电议型 号：T12597产 地：中国大陆
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T39762AHR antagonist 5 free baseAHR antagonist 5 free base
AHR antagonist 5 free base is an orally active antagonist of AHR with IC50s of ~35-150 nM in human and rodent cell lines.
价 格：￥电议型 号：T39762产 地：中国大陆
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T8294Quercetagitrininhibit,Quercetagitrin,Inhibitor
Quercetagitrin, isolated from the African Marigold (Tagetes erecta), has anti-inflammatory activity.
价 格：￥电议型 号：T8294产 地：中国大陆
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T7086Tris(benzyltriazolylmethyl)aminechemical,tagging,Inhibitor,inhibit,proteins,Tris(benzyltriazolylmeth
TBTA is a tertiary amine with three 1, 2, 3-triazole groups. It complexes with, and stabilizes, copper(I) to accelerate azide-alkyne cycloadditions, as used in click chemistry.
价 格：￥电议型 号：T7086产 地：中国大陆
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T9244σ1 Receptor antagonist-1anti-nociceptive,Sigma Receptor,cycle,σ1 Receptor antagonist1,σ1 Receptor an
σ1 Receptor antagonist-1 is a selective sigma 1 receptor antagonist.
价 格：￥电议型 号：T9244产 地：中国大陆
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T17232VidupiprantProstaglandin Receptor,AMG-853,Inhibitor,orally,acid,cAMP,phenylacetic,asthma,PGD2,AMG 00
Vidupiprant is an effective dual antagonist of CRTH2 and prostanoid D receptor with IC50s of 8 nM and 35 nM in human plasma. Vidupiprant can be used in studies about the treatment of asthma.
价 格：￥电议型 号：T17232产 地：中国大陆
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TP1935L1RAGE antagonist peptide acetateRAGE antagonist peptide acetate
RAGE antagonist peptide acetate is an advanced antagonist of glycation end products (RAGE). RAGE antagonist peptide acetate possesses anti-tumor and anti-inflammatory activities. RAGE antagonist peptide acetate prevents RAGE from binding with several of its most important ligands, including HMGB-1, S100P, and S100A4.
价 格：￥电议型 号：TP1935L1产 地：中国大陆
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T9709TRPM8 antagonist 3TRPM8 antagonist 3,TRP Channel,Transient receptor potential channels,inhibit,TRPM-
TRPM8 antagonist 3 is a blocker of TRPM8 (IC50 = 11 nM).
价 格：￥电议型 号：T9709产 地：中国大陆
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T6399AZD1981Prostaglandin Receptor,AZD 1981,AZD1981,Inhibitor,AZD-1981,inhibit
AZD1981 is an effective and specific CRTh2 (DP2) receptor antagonist (IC50: 4 nM), showing >1000-fold selectivity over more than 340 other enzymes and receptors, including DP1. AZD1981 has been used in trials studying the treatment and basic science of Asthma, Postmenopausal, Pharmakokinetic, Asthma Patients, and Drug Interaction, among others.
价 格：￥电议型 号：T6399产 地：中国大陆
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T9622MF-766EP4,arthritis,inflammation disease,AIA,inhibit,anti-tumor,MF766,MF 766,MF-766,Prostaglandin Re
MF-766 is a highly potent, selective and orally active EP4 antagonist with a Ki of 0.23 nM. It behaves as a full antagonist with an IC50 of 1.4 nM (shifted to 1.8 nM in the presence of 10% HS) in the functional assay. It can be used for cancer and inflammation diseases research[1][2].
价 格：￥电议型 号：T9622产 地：中国大陆
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T10058A2B receptor antagonist 1A-2B receptor antagonist 1,A2B receptor antagonist 1
A2B receptor antagonist 1 (EXAMPLE 9B) is a potent A2B adenosine receptor antagonist extracted from patent WO 2009157938 A1.
价 格：￥电议型 号：T10058产 地：中国大陆
