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产品数：86101
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T7101Tyrphostin AG30HER1,ErbB-1,Inhibitor,EGFR,Tyrphostin AG30,Epidermal growth factor receptor,Tyrphosti
Tyrphostin AG30 (AG30) is a potent protein tyrosine kinases (PTK) inhibitor.
价 格：￥电议型 号：T7101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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T9501EnterobactinEnterobactin
Enterobactin is a high-affinity siderophore that acquires iron for microbial systems.
价 格：￥电议型 号：T9501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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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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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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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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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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T60081BV02
BV02 is an inhibitor of 14-3-3 protein-protein interactions and can be used in studies about the treatment of chronic myeloid leukemia. BV02 disrupts hematopoietic cells expressing the IM-resistant T315I mutation and the IM-sensitive wild-type Bcr-Abl.
价 格：￥电议型 号：T60081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
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T61148Flutrimazole
Flutrimazole is an imidazole antifungal with dual anti-inflammatory and antifungal activity. Flutrimazole shows scarce transdermal penetration. Flutrimazole has the advantageous in the research of topical fungal infections with an inflammatory component.
价 格：￥电议型 号：T61148产 地：中国大陆
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T9230KM 91104V-ATPase human HSC,a3-b2 subunits,KM-91104,KM 91104,Inhibitor,KM91104,Proton Pump,cell-perme
KM 91104 is a cell permeable inhibitor of V-ATPase. KM91104 specifically targets the interaction between V-ATPase subunit A3 and subunit B2.
价 格：￥电议型 号：T9230产 地：中国大陆
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T8101Nepsilon-Acetyl-L-lysineinhibit,Nepsilon Acetyl L lysine,NepsilonAcetylLlysine,Inhibitor,Endogenous
Nepsilon-Acetyl-L-lysine is a derivative of the lysine.
价 格：￥电议型 号：T8101产 地：中国大陆
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T9279nerolidol acetatenerolidol acetate
Nerolidyl acetate is a sesquiterpenoid.
价 格：￥电议型 号：T9279产 地：中国大陆
