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T10889CRTh2 antagonist 2CRTh2 antagonist 2,CRTh-2 antagonist 2
CRTh2 antagonist 2 is a selective and potent CRTH2 antagonist, IC50≤10 nM. CRTh2 antagonist 2 can be used to study the direction of androgenic alopecia.
价 格：￥电议型 号：T10889产 地：中国大陆
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TN1089Hydroxy-β-sanshool
Hydroxy-β-sanshool is a pungent compound obtained from Zanthoxylum piperitum.
价 格：￥电议型 号：TN1089产 地：中国大陆
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TP1086Men 10376 TFA(135306-85-3,free)Men 10376 TFA(135306853,free),Men 10376 TFA(135306 85 3,free)
Men 10376 TFA is an effective and selective tachykinin nk-2 receptor antagonist with a K I value of 4.4 M for the nk-2 receptor in the small intestine of rats.
价 格：￥电议型 号：TP1086产 地：中国大陆
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TQ0289LY450108Inhibitor,inhibit,AMPA,Parkinson’s,LY 450108,depression,iGluR,LY-450108,LY450108,Ionotropic
LY450108 is a potentiator of the AMPA receptor that can be used in Parkinson´s disease studies.
价 格：￥电议型 号：TQ0289产 地：中国大陆
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T6068MK-5108MK 5108,VX689,Aurora Kinase,VX 689,inhibit,Autophagy,MK-5108,Inhibitor
MK-5108 is a highly potent and specific Aurora-A kinase inhibitor with an IC50 value of 0.064 nM.
价 格：￥电议型 号：T6068产 地：中国大陆
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TN1108Kaempferol 3-O-sophorosideKaempferol 3 O sophoroside,Kaempferol 3Osophoroside,Inhibitor,inhibit
Kaempferol 3-O-beta-sophoroside has antibacterial and antiviral activities.
价 格：￥电议型 号：TN1108产 地：中国大陆
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T10874CP-060CP060,CP 060
CP-?060 is a potent Ca2+ antagonist and inhibits Ca2+ overload with antioxidant and cardioprotective activities.
价 格：￥电议型 号：T10874产 地：中国大陆
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T10852CNS-5161 hydrochloride
CNS-5161 hydrochloride is a new antagonist of NMDA ion-channel. It interacts with the NMDA receptor/ion channel site to produce a noncompetitive blockade of the actions of glutamate.
价 格：￥电议型 号：T10852产 地：中国大陆
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T10859COH34
COH34 is a selective inhibitor of PARG with an IC50 of 0.37 nM and a Kd of 0.547 μM. COH34 prolongs PARylation at DNA lesions and traps DNA repair factors.
价 格：￥电议型 号：T10859产 地：中国大陆
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T10883LCRA-026440 hydrochloride
CRA-026440 hydrochloride is a potent and broad-spectrum HDAC inhibitor. CRA-026440 hydrochloride exhibits Ki values against recombinant HDAC isoenzymes HDAC1, HDAC2, HDAC3, HDAC6, HDAC8, and HDAC10 are 4 nM, 14 nM, 11 nM, 15 nM, 7 nM, and 20 nM, respectively. CRA-026440 hydrochloride exhibits antitumor and antiangiogenic activities.
价 格：￥电议型 号：T10883L产 地：中国大陆
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T8649TMBIM6 antagonist-1TMBIM-6 antagonist-1,TMBIM6 antagonist 1,HT1080,SKBR3,TMBIM6 antagonist1,MCF7,Mam
BIA is a bax inhibitor
价 格：￥电议型 号：T8649产 地：中国大陆
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TN2108ProtohypericinProtohypericin,naphthodianthrone,Inhibitor,NSCLC,inhibit
Protohypericin is a naturally occurring naphthodianthrone derived from plant Hypericum perforatum.Radioiodinated protohypericin is used in Tumor necrosis targeted radiotherapy. Protohypericin exhibits photocytotoxicity.
价 格：￥电议型 号：TN2108产 地：中国大陆
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T10837Clocapramine dihydrochloride hydrateClocapramine dihydrochloride hydrate
Clocapramine dihydrochloride hydrate is an antagonist of the 5-HT2A and D2 receptors.
价 格：￥电议型 号：T10837产 地：中国大陆
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T10863Complement C5-IN-1Complement C-5-IN-1,Complement C5 IN 1,Complement C5IN1
Complement C5-IN-1 is a small-molecule inhibitor of complement component 5 protein (C5).
价 格：￥电议型 号：T10863产 地：中国大陆
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T10896LCSRM617 hydrochloride
CSRM617 hydrochloride is a selective small-molecule inhibitor of the transcription factor ONECUT2 ( OC2, a master regulator of androgen receptor) with a K d of 7.43 uM in SPR assays, directly binds to OC2-HOX domain. CSRM617 hydrochloride induces apoptosis through the appearance of cleaved Caspase-3 and PARP. CSRM617 hydrochloride is well tolerated in the mouse model of prostate cancer [1]
价 格：￥电议型 号：T10896L产 地：中国大陆
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TN1085Dehydrotumulosic acidinhibit,Inhibitor,Dehydrotumulosic acid
Dehydrotumulosic acid shows anti-inflammatory activity.
价 格：￥电议型 号：TN1085产 地：中国大陆
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T101083-Bromocytisine
3-Bromocytisine is an effective agonist of nAChR (IC50s: 0.28, 0.30 and 31.6 nM for hα4β4, hα4β2, and hα7).
价 格：￥电议型 号：T10108产 地：中国大陆
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T61112SLF1081851
SLF1081851 is a Spns2 inhibitor. SLF1081851 inhibits S1P release with IC50 of 1.93 μM.
价 格：￥电议型 号：T61112产 地：中国大陆
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T10824cis-Urocanic acid
cis-Urocanic acid is a 5-HT2A receptor agonist (Kd: 4.6 nM). It is an immune modulator that induces immunosuppression by binding to the 5-HT2A receptor.
价 格：￥电议型 号：T10824产 地：中国大陆
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T60108PDGFR Tyrosine Kinase Inhibitor III
PDGFR Tyrosine Kinase Inhibitor III (PDGF Receptor Tyrosine Kinase Inhibitor III) is a multikinase inhibitor that inhibits PDGFR, EGFR, FGFR, PKA, and PKC, respectively. PDGFR Tyrosine Kinase Inhibitor III can be used for the research of amyotrophic lateral sclerosis [1].
价 格：￥电议型 号：T60108产 地：中国大陆
