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产品数：86101
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TN4782Picein
Picein is derived from Picrorhiza kurroa and shows antioxidant properties.
价 格：￥电议型 号：TN4782产 地：中国大陆
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T8951JTP 0819958 - HOIPIN-1JTP 0819958 HOIPIN1,JTP 0819958 HOIPIN 1
JTP-0819958 is a selective linear ubiquitin chain assembly complex (LUBAC) inhibitor with an IC50 of 2.8 μM[1]. JTP-0819958 suppress LUBAC-mediated NF-kB activation in vitro[2].
价 格：￥电议型 号：T8951产 地：中国大陆
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T7360GSK2018682LPL Receptor,Inhibitor,inhibit,Lysophospholipid Receptor,GSK-2018682,GSK 2018682,GSK201868
GSK2018682 is an agonist of sphingosine-1-phosphate receptor (s1p1) and (s1p5) agonist(pEC50s of 7.7 and 7.2,respectively).
价 格：￥电议型 号：T7360产 地：中国大陆
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T9307(E)-3-(3,4-dichlorophenyl)-N-(2-(4-(methylsulfonyl)piperazin-1-yl)-2-oxoethyl)acrylamide(E)3(3,4dich
(E)-3-(3,4-dichlorophenyl)-N-(2-(4-(methylsulfonyl)piperazin-1-yl)-2-oxoethyl)acrylamide is a chemical compound.
价 格：￥电议型 号：T9307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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T95101,2-Distearoyl-sn-glycero-3-phosphorylcholineinhibit,lipid,liposomes,1,2Distearoylsnglycero3phosphor
L-ALPHA-PHOSPHATIDYLCHOLINE, DISTEAROYL is a cylindrical-shaped lipid used to synthesize liposomes. L-ALPHA-PHOSPHATIDYLCHOLINE, DISTEAROYL is the lipid component in the lipid nanoparticle (LNP) system.
价 格：￥电议型 号：T9510产 地：中国大陆
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T60231N-[2-nitro-4-(trifluoromethyl)phenyl]piperazineN[2NITRO4(TRIFLUOROMETHYL)PHENYL]PIPERAZINE
N-[2-nitro-4-(trifluoromethyl)phenyl]piperazine is a bioactive substances.
价 格：￥电议型 号：T60231产 地：中国大陆
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T7044NorepinephrineAutophagy,L-Noradrenaline,Beta Receptor,inhibit,Levarterenol,Norepinephrine,Inhibitor,
Norepinephrine can stimulate apoptosis in adult rat ventricular myocytes by activation of the β-adrenergic pathway. It can up-regulate the expression of vascular endothelial growth factor, matrix metalloproteinase (MMP)-2, and MMP-9 in nasopharyngeal carcinoma tumour cells.
价 格：￥电议型 号：T7044产 地：中国大陆
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T8502N-(1-benzyl-4-piperidyl)adamantane-1-carboxamideN(1benzyl4piperidyl)adamantane1carboxamide,N (1 benz
N-(1-benzyl-4-piperidyl)adamantane-1-carboxamide inhibiting the entry of Ebola virus in host cells by binding to the surface glycoprotein, the compound inhibited the Ebola virus with EC50 of 3.9 μM.
价 格：￥电议型 号：T8502产 地：中国大陆
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T38699Piperafizine Ainhibit,Piperafizine A,N-monoalkylated plinabulin,piperafizine,anti-cancer,Inhibitor
Piperafizine A is isolated from Streptoverticillium aspergilloides and potentiates vincristine antitumor potency.
价 格：￥电议型 号：T38699产 地：中国大陆
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TN7041(-)-Epipodophyllotoxin( ) Epipodophyllotoxin,spindle,antiproliferative,Apoptosis,American,904166,can
(-)-Epipodophyllotoxin (2) is an antiproliferative agent against cancer cells with GI50s of 0.36 and 0.24 μM in HeLa cells and MCF-7 cells, respectively. (-)-Epipodophyllotoxin can inhibit mitotic spindle assembly in vitro.
价 格：￥电议型 号：TN7041产 地：中国大陆
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T7854Bortezomib-pinanediolBortezomibpinanediol,Bortezomib pinanediol
Bortezomib-pinanediol is a proteasome inhibitor. is a prodrug of Bortezomib.
价 格：￥电议型 号：T7854产 地：中国大陆
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T3148MK-571 sodiumMRP4,Lysophospholipid Receptor,human mast cells,LAD2,MK 571 sodium,MRP1,Leukotriene Rec
MK-571 is a selective, orally active antagonist of the CysLT1 receptor. MK571 is a multidrug resistance protein-2 (ABCC2, Mrp2) inhibitor used to demonstrate the role of Mrp2 in the cellular efflux of drugs, xenobiotics, and their conjugates. MK571 can inhibit the synthesis of K-4′-O-GlcA (19.7 μM). MK571 dose-dependently inhibits the intracellular biosynthesis of all flavonol sulphates and glucuronides by Caco-2 cells. MK571 significantly inhibits phase-2 conjugation of kaempferol by cell-free
价 格：￥电议型 号：T3148产 地：中国大陆
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T9552BAZ1A-IN-1leukemia,breast cancer,Epigenetic Reader Domain,BAZ1A IN 1,cancer,ZR-75–30,BAZ1A,BAZ1AIN1,
BAZ1A-IN-1 is a potent BAZ1A inhibitor with the KD value of 0.52 μM for the BAZ1A bromodomain. BAZ1A-IN-1 shows good anti-survival activity against cancer cell lines with high BAZ1A expression, but weak or no activity against cancer cells with low BAZ1A expression.
价 格：￥电议型 号：T9552产 地：中国大陆
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T7865DanofloxacinInhibitor,Antibiotic,DNA-gyrase,respiratory,mycoplasma,inhibit,Fluoroquinolone,Danofloxa
Danofloxacin is a fluoroquinolone antibiotic used in veterinary medicine.
价 格：￥电议型 号：T7865产 地：中国大陆
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T6727VU0364770inhibit,Metabotropic glutamate receptors,VU0364770,VU-0364770,Inhibitor,mGluR
VU 0364770(EC50=1.1 μM), a positive allosteric modulator(PAM) of mGlu4, shows insignificant activity at 68 other receptors, including other mGlu subtypes.
价 格：￥电议型 号：T6727产 地：中国大陆
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TN2252Syrosingopinecancer,Syrosingopine,NAD+,Su-3118,MCTs,Su 3118,synthetic lethality,inhibit,metformin,la
Syrosingopine has selective depleting effect on brain amines is potentiated by combined treatment with disulfiram or fusaric acid, a dopamine beta-hydroxylase inhibitor.
价 格：￥电议型 号：TN2252产 地：中国大陆
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T9710DazcapistatProteasome,Dazcapistat,inhibit,Inhibitor
Dazcapistat is a potent calpain inhibitor, with IC50s of <3 μM for calpain 1, calpain 2 and calpain 9, respectively.
价 格：￥电议型 号：T9710产 地：中国大陆
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T7550BarnidipineBarnidipine,Inhibitor,Ca2+ channels,Calcium Channel,inhibit,Ca channels
Barnidipine is a calcium channel blocker.
价 格：￥电议型 号：T7550产 地：中国大陆
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T6645Ropivacaine hydrochloride monohydratePotassium Channel,hypertension,Na channels,pain,K(2P),neuropath
Ropivacaine HCl is an anaesthetic agent and blocks impulse conduction in nerve fibres through inhibiting sodium ion influx reversibly.
价 格：￥电议型 号：T6645产 地：中国大陆
