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T24642YH-306
YH-306 is a modulator of the FAK signaling pathway that acts by suppressing colorectal tumor growth and metastasis.
价 格：￥电议型 号：T24642产 地：中国大陆
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T6800CCF642calcium,Inhibitor,PDI,CCF642,apoptosis,isomerases,disulfide,myeloma,CCF-642,protein,multiple,r
CCF642 is a novel PDI-inhibiting compound with antimyeloma activity.
价 格：￥电议型 号：T6800产 地：中国大陆
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T86424-CMTBshort-chain,4 CMTB,fatty,acids,ECL2,FFAR,Free Fatty Acid Receptor,4CMTB,GPCRs,4-CMTB,ago-allos
4-CMTB is a selective agonist of FFA2 and GPR43.It also is a positive allosteric modulator (pEC50=6.38).
价 格：￥电议型 号：T8642产 地：中国大陆
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T6425BTZ043 RacemateBenzothiazinone10526038,inhibit,Benzothiazinone-10526038,BTZ043 Racemate,BTZ 10526038
BTZ043 racemate is a decaprenylphosphoryl-β-D-ribose 2´-epimerase (DprE1) inhibitor, used as a new antimycobacterial agent.
价 格：￥电议型 号：T6425产 地：中国大陆
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T6424Bromfenac SodiumInhibitor,inhibit,Bromfenac,Cyclooxygenase,HLEC-B3,Bromfenac Sodium,COX,ocular infla
Bromfenac Sodium is a nonsteroidal anti-inflammatory drug (NSAID), which has anti-inflammatory activity and may block prostaglandin synthesis by inhibiting cyclooxygenase 1 and 2.
价 格：￥电议型 号：T6424产 地：中国大陆
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T6422Brimonidine TartrateUK-14304,UK14304,AGN190342,Brimonidine,Adrenergic Receptor,AGN-190342,AGN 190342
Brimonidine tartrate is a quinoxaline derivative and adrenergic α-2 receptor agonist (EC50: 0.45 nM) that is used to manage intraocular pressure associated with open-angle glaucoma or ocular hypertension.
价 格：￥电议型 号：T6422产 地：中国大陆
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T6429Caffeic Acid Phenethyl EsterApoptosis,Caffeic Acid Phenethyl Ester,Nuclear factor-kappaB,Inhibitor,N
Caffeic Acid Phenethyl Ester (CAPE) inhibits the activation of nuclear transcription factor NF-kappa B and may suppress p70S6K and Akt-driven signaling pathways, with antineoplastic, cytoprotective and immunomodulating activities. CAPE is the phenethyl alcohol ester of caffeic acid and a bioactive component of honeybee hive propolis. In addition, CAPE inhibits PDGF-induced proliferation of vascular smooth muscle cells through the activation of p38 mitogen-activated protein kinase (MAPK) and hypo
价 格：￥电议型 号：T6429产 地：中国大陆
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TP1459LGly-Arg-Gly-Asp-Ser acetate(96426-21-0 free base)GlyArgGlyAspSer acetate(96426210 free base),Gly Arg
Gly-Arg-Gly-Asp-Ser (GRGDS) acetate is a cell binding protein domain derived from the cell-binding region of fibronectin.
价 格：￥电议型 号：TP1459L产 地：中国大陆
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T6427ButeinPDE4,Epidermal growth factor receptor,Inhibitor,EGFR,MAPK,ErbB-1,Apoptosis,Autophagy,FoxO3a,in
Butein, a plant polyphenol, is isolated from Rhus verniciflua. It can inhibit the activation of protein tyrosine kinase, NF-κB and STAT3, and also can inhibit EGFR.
价 格：￥电议型 号：T6427产 地：中国大陆
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T6428BV6inhibit,Inhibitor,BV6,IAP,BV-6,BV 6
BV6 is an antagonist of c-IAP1 and XIAP, members of the inhibitors of apoptosis (IAP) family.
价 格：￥电议型 号：T6428产 地：中国大陆
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T16425PA452PA452,PA-452
PA452 is a selective antagonist of retinoic X receptor (RXR) and suppresses the effect of Retinoic acid on Th1/Th2 development.
价 格：￥电议型 号：T16425产 地：中国大陆
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T6420BMS-707035BMS 707035,HIV-1 integrase strand transfer,HIV,Human immunodeficiency virus,antiviral,BMS7
BMS-707035 is a specific HIV-I integrase (IN) inhibitor with IC50 of 15 nM. Phase 2.
价 格：￥电议型 号：T6420产 地：中国大陆
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T6423BRL-15572 dihydrochlorideh5-HT1D,BRL 15572 dihydrochloride,BRL15572,BRL 15572,5-HT Receptor,BRL-1557
BRL-15572 is a 5-HT1D receptor antagonist with pKi of 7.9, also shows a considerable affinity at 5-HT1A and 5-HT2B receptors, exhibiting 60-fold selectivity over 5-HT1B receptor.
价 格：￥电议型 号：T6423产 地：中国大陆
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T9642ZW4864 free baseZW4864 free base
ZW4864 free base is an orally active and selective inhibitor of β catenin/B-Cell lymphoma 9 protein?protein interaction (β catenin/BCL9 PPI, Ki= 0.76 μM, IC50= 0.87 μM).
价 格：￥电议型 号：T9642产 地：中国大陆
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T6426Buclizine dihydrochlorideteratogen,Inhibitor,MCF-7,anti-tumor activity,antiallergic,antihistamine,in
Buclizine HCl is the hydrochloride salt form of buclizine, a piperazine histamine H1 receptor antagonist with primarily antiemetic and antivertigo activities. Buclizine binds to and blocks the histamine H1 receptor, thereby preventing the symptoms that are caused by histamine activity. Buclizine exerts its anti-emetic effect by binding to and blocking the muscarinic and histamine receptors in the vomiting center of the central nervous system (CNS). This may prevent activation of the chemorecepto
价 格：￥电议型 号：T6426产 地：中国大陆
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T7642CilostamideOPC-3689,OPC 3689,Cilostamide,Phosphodiesterase (PDE),Inhibitor,inhibit
Cilostamide is a selective phosphodiesterase (PDE)3A and PDE3B inhibitor(IC50 values of 27 and 50 nM, respectively)
价 格：￥电议型 号：T7642产 地：中国大陆
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T6421BRD73954Inhibitor,BRD73954,Ac-Tubulin,inhibit,α-tubulin acetylation,HeLa cells,BRD-73954,BRD 73954,H
BRD73954, an effective and specific HDAC inhibitor, which is with IC50 of 36 nM and 120 nM for HDAC6 and HDAC8, respectively.
价 格：￥电议型 号：T6421产 地：中国大陆
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T12642(R)-Simurosertib
(R)-Simurosertib is an inhibitor of the ATP-competitive cell division cycle 7 (CDC7) kinase.
价 格：￥电议型 号：T12642产 地：中国大陆
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T6108Ki16425Debio 0719
Ki16425 is a competitive, potent and reversible antagonist to LPA1, LPA2 and LPA3 with Ki of 0.34 μM, 6.5 μM and 0.93 μM, respectively.
价 格：￥电议型 号：T6108产 地：中国大陆
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T5642TegatrabetanBC2059
BC2059 is a small molecule inhibitor of the Wnt/beta-catenin pathway with potential antineoplastic activity.
价 格：￥电议型 号：T5642产 地：中国大陆
