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T7691NSC 3852NSC 3852
NSC 3852 is a potent inhibitor of histone deacetylase.
价 格：￥电议型 号：T7691产 地：中国大陆
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T8408GKT136901peroxynitrite,scavenger,neurodegeneration,NOX1/4,NADPH,oxidase,inhibit,NOX,NADPH Oxidase,GK
GKT136901 is an inhibitor of NOX1/4.It acts as Selective and Direct Scavenger of Peroxynitrite
价 格：￥电议型 号：T8408产 地：中国大陆
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T8116Azulenenaphthalene,chamomile,scaffold,Azulene,oil,Cyclopentacycloheptene,distillation,inhibit,Human
Bicyclo[5.3.0]Decapentaene is a natural product.
价 格：￥电议型 号：T8116产 地：中国大陆
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T87944-MMPBLOX,4 MMPB,radical,Inhibitor,inhibit,4-MMPB,scavenging,Lipoxygenase,cancer,Apoptosis,4MMPB,inh
15-Lipoxygenase Inhibitor 1 is a selective inhibitor of 15-lipoxygenase, with an IC50 of 18 μM. 4-MMPB has IC50s of 19.5 μM and 19.1 μM for soybean 15-lipoxygenase (SLO) and human 15-lipoxygenase-1 (15-LOX-1), respectively. 4-MMPB has potential for the research of prostate cancer.
价 格：￥电议型 号：T8794产 地：中国大陆
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T9929RamucirumabRamucirumab,NSCLC,non–small-cell lung cancer,gastric cancer,Inhibitor,VEGFR,Vascular endo
Ramucirumab is a human VEGFR-2 antagonist for the treatment of solid tumors.
价 格：￥电议型 号：T9929产 地：中国大陆
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T9636DalpiciclibMCF7,BT-474/T,Cyclin dependent kinase,Eca 109,MCF7/TR,and KYSE-510 ESCC,SHR6390,Inhibitor
Dalpiciclib is a highly selective, orally bioavailable, and comparable potency inhibitor of CDK4 and CKD6 with IC50s of 12.4?nM and 9.9?nM, respectively. Dalpiciclib exerts potent antitumor activity in esophageal squamous cell carcinoma by inhibiting phosphorylated tumor suppressor retinoblastoma protein (Rb) and inducing G1 cell cycle arrest.
价 格：￥电议型 号：T9636产 地：中国大陆
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T7525DidoxInhibitor,DNA/RNA Synthesis,inhibit,Didox,NSC 324360,NSC324360
Didox is a synthetic ribonucleotide reductase (RR) inhibitor that has been found to reduce the levels of oxidative injury markers in the brains of HIV patients with dementia.
价 格：￥电议型 号：T7525产 地：中国大陆
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T6517GolvatinibE7050,Golvatinib,c-Met/HGFR,VEGFR,Inhibitor,Vascular endothelial growth factor receptor,E
Golvatinib is an orally bioavailable dual kinase inhibitor of c-Met (hepatocyte growth factor receptor) and VEGFR-2 (vascular endothelial growth factor receptor-2) tyrosine kinases with potential antineoplastic activity. c-Met/VEGFR kinase inhibitor E7050 binds to and inhibits the activities of both c-Met and VEGFR-2, which may inhibit tumor cell growth and survival of tumor cells that overexpress these receptor tyrosine kinases. c-Met and VEGFR-2 are upregulated in a variety of tumor cell types
价 格：￥电议型 号：T6517产 地：中国大陆
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T9183RalmitarontRO 6889450,TAAR1,Schizoaffective Disorder,Inhibitor,SCZ,Ralmitaront,Negative Symptom,inhi
Ralmitaront is a potent, orally active partial agonist of the trace amine-associated receptor 1 (TAAR1).
价 格：￥电议型 号：T9183产 地：中国大陆
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T8656CAY10404Bcl-XL,CAY10404,cancer,COX,anti-inflammatory,Bcl-2,Apoptosis,Akt,H-1703,Cyclooxygenase,NSCLC
CAY10404 is a potent and highly selective inhibitor of COX-2 and COX-1. It is also a potent inhibitor of PKB/Akt and MAPK signalling pathways and induces apoptosis in NSCLC cells, with analgesic, anti-inflammatory and anti-cancer activities.
价 格：￥电议型 号：T8656产 地：中国大陆
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T8157CenthaquinPMZ2010,inhibit,systemic vascular resistance,Inhibitor,Centhaquin,haemorrhagic shock,PMZ 2
Centhaquine is an adrenergic receptor potentially for the treatment of postoperative pain and for the resuscitation of hypovolemic shock
价 格：￥电议型 号：T8157产 地：中国大陆
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T7392RevefenacinRevefenacin,TD4208,TD 4208,inhibit,Muscarinic acetylcholine receptor,Inhibitor,mAChR,GSK
Revefenacin is a mAChR antagonist has a high affinity on M3 receptor( Ki : 0.18 nM),and potentially useful for the treatment of respiratory disease.
价 格：￥电议型 号：T7392产 地：中国大陆
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T7133Anagliptinlipid‐lowering,smooth muscle cell,SK0403,inhibit,DPP-4,Anagliptin,Dipeptidyl Peptidase,DPP
Anagliptin is a potent Inhibitor of DPP-4(IC50 of 3.8 nM), for the treatment of type 2 diabetes mellitus.
价 格：￥电议型 号：T7133产 地：中国大陆
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T8342BRD9876Kinesin,microtubule,Inhibitor,BRD9876,BMSC,multiple,myeloma,α4-α6,CD34,tyrosine,ATP,MM1S,G2/M
BRD9876 is a selective inhibitor of MM1S growth.
价 格：￥电议型 号：T8342产 地：中国大陆
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T7186CZC-8004CZC 8004,HER1,Vascular endothelial growth factor receptor,ErbB-1,Epidermal growth factor rec
CZC-8004 is a pan-kinase(ABL kinase) inhibitor and binds a range of tyrosine kinases.
价 格：￥电议型 号：T7186产 地：中国大陆
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T7945SU14813c-Kit,Inhibitor,VEGFR,Vascular endothelial growth factor receptor,SU 14813,PDGFR,CD117,Platel
SU14813 is a multi-receptor tyrosine kinase inhibitor with potent antiangiogenesis and antitumor activity (IC50s of 50, 2, 4, 15 nM for VEGFR2, VEGFR1, PDGFRβ and KIT).
价 格：￥电议型 号：T7945产 地：中国大陆
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T6455CP-91149diabetes,CP91149,CP-91149,A549,CP 91149,NSCLC,Inhibitor,inhibit
CP-91149 is a selective glycogen phosphorylase (GP) inhibitor with IC50 of 0.13 μM in the presence of glucose, 5- to 10-fold less potent in the absence of glucose.
价 格：￥电议型 号：T6455产 地：中国大陆
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T60078NSC2805
NSC2805 is an inhibitor of WWP2, an E3 ubiquitin ligase with an IC50 of 0.38 μM. NSC2805 can be used in anticancer studies.
价 格：￥电议型 号：T60078产 地：中国大陆
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T8984FLTX1cancer,Estrogen Receptor/ERR,FLTX1,FLTX 1,Inhibitor,fluorescent,Tamoxifen,antiestrogenic,inhibi
FLTX1, a fluorescent Tamoxifen derivative that can specifically label intracellular Tamoxifen-binding sites (estrogen receptors) under permeabilized and non-permeabilized conditions. FLTX1 exhibits the potent antiestrogenic properties of Tamoxifen in breast cancer cells. FLTX1 is devoid of the estrogenic agonistic effect on the uterus.
价 格：￥电议型 号：T8984产 地：中国大陆
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T8213IsolinderalactoneSurvivin,VEGFR,Isolinderalactone,Vascular endothelial growth factor receptor,Inhibi
Isolinderalactone shows anti-inflammatory and anticancer capacity, and it exhibits moderate iNOS inhibitory activity, with the IC50 value of 0.30 uM.
价 格：￥电议型 号：T8213产 地：中国大陆
