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T7519RS-127445 hydrochlorideInhibitor,RS127445,5-HT Receptor,inhibit,RS-127445,RS127445 hydrochloride,Ser
RS 127445 is a selective, high affinity, orally bioavailable 5-HT2B receptor antagonist(pKi : 9.5).
价 格：￥电议型 号：T7519产 地：中国大陆
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T10436AZD4573AZD 4573,inhibit,CDK,AZD4573,AZD-4573,Inhibitor,Cyclin dependent kinase
AZD4573 is an effective and selective CDK9 inhibitor (IC50: <4 nM). It enables transient target engagement for the treatment of hematologic malignancies.
价 格：￥电议型 号：T10436产 地：中国大陆
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TN2080Pinoresinolapoptotic,sensitizer,Pinoresinol,caterpillar,inhibit,cancer,Apoptosis,Inhibitor,lignol,gl
Pinoresinol has antiinflammatory, hepatoprotective, and fungicidal activities, it can protect pial microcirculation from I-reperfusion injury, to increase nitric oxide release and to reduce oxidative stress preserving pial blood flow distribution; it may exert pharmacologically interesting effects via modulation of the insulin-like signalling pathway in C.elegans. Pinoresinol causes an upregulation of the CDK inhibitor p21(WAF1/Cip1) both at mRNA and protein levels, inhibits NF-kappaB and activa
价 格：￥电议型 号：TN2080产 地：中国大陆
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T27026LCJ-13,610 hydrochlorideCJ 13,610 hydrochloride,CJ13,610 hydrochloride
CJ-13,610 hydrochloride is an orally active nonredox-type inhibitor of 5-LOX and can be used in studies about the prevention of untoward pathophysiological effects of LTs.
价 格：￥电议型 号：T27026L产 地：中国大陆
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T12569LPSB-12379 ditriethylamine saltPSB 12379 disodium,PSB12379 disodium
PSB-12379 ditriethylamine salt, a nucleotide analogue, is a potent Ecto-5´-Nucleotidase (CD73) inhibitor with Kis of 9.03 nM (rat) and 2.21 nM (human).
价 格：￥电议型 号：T12569L产 地：中国大陆
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TQ0050NCGC00244536NCGC 00244536,inhibit,Histone Demethylase,NCGC00244536,Inhibitor,NCGC-00244536
NCGC00244536 is a potent KDM4B inhibitor (IC50: 10 nM).
价 格：￥电议型 号：TQ0050产 地：中国大陆
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T6S0657Isorhynchophyllineinhibit,Inhibitor,Isorhynchophylline
1. Isorhyncophylline and rhyncophylline can directly inhibit the contractile responses induced by several agonists in small blood vessels of rat, they also can inhibit the hypertensive effect of angiotensin Ⅱ.
价 格：￥电议型 号：T6S0657产 地：中国大陆
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T6725VU 0357121inhibit,VU-0357121,VU 0357121,VU0357121,Inhibitor,Metabotropic glutamate receptors,mGluR
VU0357121, a positive allosteric modulator of mGlu5 (EC50: 33 nM), is inactive or very weakly antagonizing at other mGlu receptor subtypes.
价 格：￥电议型 号：T6725产 地：中国大陆
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TP1179LPorcine dynorphin A(1-13) acetatePorcine dynorphin A(113) acetate,Porcine dynorphin A(1 13) acetate
Porcine dynorphin A(1-13) acetate is a potent, endogenous κ opioid receptor agonist and is antinociceptive at physiological concentrations. Exposure to dynorphin A (1-13) causes acute increases in [Ca2+]i in individual neurons similar to increases seen with acute NMDA treatment.
价 格：￥电议型 号：TP1179L产 地：中国大陆
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T9184LCompound 3344 hydrochlorideCompound 3344 hydrochloride
Compound 3344 hydrochloride is an inhibitor of KRAS-effector interactions，with an affnity of 126nm.
价 格：￥电议型 号：T9184L产 地：中国大陆
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T89102-AMINO-5-PHENYL-THIOPHENE-3-CARBOXYLIC2 AMINO 5 PHENYL THIOPHENE 3 CARBOXYLIC,2AMINO5PHENYLTHIOPHEN
2-AMINO-5-PHENYL-THIOPHENE-3-CARBOXYLIC is Inhibitior of IKKβ.
价 格：￥电议型 号：T8910产 地：中国大陆
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T7665[Leu5]-Enkephalin TFA(58822-25-6(free bas))[Leu5] Enkephalin TFA(58822 25 6(free bas)),[Leu-5]-Enkep
[Leu5]-Enkephalin is the most potent δ-receptor ago
价 格：￥电议型 号：T7665产 地：中国大陆
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T15612JH-VIII-157-02CD246,Cluster of differentiation 246,inhibit,Anaplastic lymphoma kinase,Anaplastic lym
JH-VIII-157-02 is an inhibitor of ALK and inhibits echinoderm microtubule-associated protein-like 4-ALK (EML4-ALK) with IC50s of 2 nM for EML4-ALK G1202R, EML4-ALKwt, EML4-ALK C1156Y, EML4-ALK F1174L, and EML4-ALK F1174L.
价 格：￥电议型 号：T15612产 地：中国大陆
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T9179CLP-3094LNCaP,Inhibitor,Androgen Receptor,CLP3094,inhibit,prostate,CLP 3094,resistance,CLP-3094,anti
CLP-3094 is a potent androgen receptor BF3 (binding function 3) inhibitor. BF3-IN-1 inhibits AR transcriptional activity with IC50 of 4 μM. CLP-3094 is a selective and potent GPR142 antagonist.
价 格：￥电议型 号：T9179产 地：中国大陆
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T6557KU-0060648mTOR,inhibit,KU-0060648,Phosphoinositide 3-kinase,Inhibitor,Mammalian target of Rapamycin,
KU-0060648 is a dual inhibitor of DNA-PK and PI3Kα, PI3Kβ, PI3Kδ with IC50 of 8.6 nM and 4 nM, 0.5 nM, 0.1 nM respectively, less inhibition of PI3Kγ with IC50 of 0.59 μM.
价 格：￥电议型 号：T6557产 地：中国大陆
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T12721Rho-Kinase-IN-1Rho Kinase IN 1,RhoKinaseIN1
Rho-Kinase-IN-1 is an inhibitor of ROCK with Kis of 30.5 nM and 3.9 nM for ROCK1 and ROCK2, respectively. Rho-Kinase-IN-1 can be used in studies about excessive cell proliferation, remodeling, edema and inflammation diseases.
价 格：￥电议型 号：T12721产 地：中国大陆
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T87246-Methoxydihydrosanguinarinecancer,6-Methoxydihydrosanguinarine,SF-268,6 Methoxydihydrosanguinarine,
6-Methoxydihydrosanguinarine is a natural product. 6-Methoxydihydrosanguinarine shows strong cytotoxicity against MCF-7 and SF-268 cell lines with IC50 values of 0.61 μM and 0.54 μM, respectively.It has antibacterial activity against Methicillin-resistant Staphylococcus aureus (MRSA) strains with minimum inhibitory concentrations (MICs) ranging from1.9 to 3.9 microg/ml
价 格：￥电议型 号：T8724产 地：中国大陆
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T8192Pentacosanoic acidesters,fatty,Endogenous Metabolite,adrenoleukodystrophy,Inhibitor,cholesterol,acid
Pentacosanoic acid, belongs to the class of organic compounds known as very long-chain fatty acids.
价 格：￥电议型 号：T8192产 地：中国大陆
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TP1895L1KYL acetate(676657-00-4 free base)KYL acetate(676657 00 4 free base),KYL acetate(676657004 free base
EphA4 receptor tyrosine kinase inhibitor (Kd = 0.8 μM); inhibits EphA4-EphrinA5 interactions (IC50 = 6.34 μM). Prevents AβO induced synaptic damage, dendritic spine loss and prevents the blocking of LTP in hippocampal CA3-CA1 transmissions. Exhibits a long half life in cell culture media (8 and 12 hours in PC3 and C2C12 media respectively). Neuroprotective.
价 格：￥电议型 号：TP1895L1产 地：中国大陆
