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产品数：86101
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T7789DRB5,6-Dichlorobenzimidazole riboside,DRB,inhibit,Inhibitor,CDK,Cyclin dependent kinase
DRB is a nucleoside analog that inhibits several carboxyl-terminal domain (CTD) kinases including casein kinase II (IC50 range of 4-10 μM)
价 格：￥电议型 号：T7789产 地：中国大陆
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T78266-Chloropurine riboside6 Chloropurine riboside,6Chloropurine riboside
6-Chloropurine riboside is a chemical compound
价 格：￥电议型 号：T7826产 地：中国大陆
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T7655FialuridineFialuridine,NSC678514,DRG 0098,Orthopoxvirus,DNA/RNA Synthesis,DRG0098,inhibit,NSC 678514
Fialuridine is a DNA-directed DNA polymerase inhibitor potentially for the treatment of HBV infection with potent activity against hepatitis B virus in vitro and in vivo.
价 格：￥电议型 号：T7655产 地：中国大陆
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T7586trifaroteneRAR/RXR,inhibit,trifarotene,CD-5789,Autophagy,RAR,Retinoid X receptors,acne,CD 5789,Retin
trifarotene is a potent and selective RARγ agonist with 65-fold and 16-fold selectivitiy for the RARγ (EC50=7.7 nM) over RARα (EC50=500 nM) and RARβ (EC50=125 nM).
价 格：￥电议型 号：T7586产 地：中国大陆
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T9786Lu AF27139Inhibitor,P2XRs,oral,P2X7,rodent-active,Lu AF 27139,CNS-penetrant,CNS,Lu AF27139,Lu AF-271
Lu AF27139 is an effective and selective antagonist of P2X7 receptor (IC50s of 12 and 2.4 nM for human and rat, Kis of 22, 54, and 13 nM for mouse, human, and rat, respectively). Lu AF27139 can be used in CNS diseases studies.
价 格：￥电议型 号：T9786产 地：中国大陆
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TP13782-Furoyl-LIGRLO-amide TFA(729589-58-6 free base)2 Furoyl LIGRLO amide TFA(729589 58 6 free base),2Fu
2-Furoyl-LIGRLO-amide is a potent and selective protease-activated receptor 2 (PAR2) agonist.
价 格：￥电议型 号：TP1378产 地：中国大陆
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TP1370LCrosstide TFA(171783-05-4 free base)Crosstide TFA(171783 05 4 free base),Crosstide TFA(171783054 fre
Crosstide is a peptide analog of glycogen synthase kinase α/β fusion protein sequence which is a substrate for Akt.
价 格：￥电议型 号：TP1370L产 地：中国大陆
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T7885Afuresertib hydrochlorideAfuresertib,PKC,Protein kinase C,Akt,PKB,Rho-kinase,GSK2110183,ROK,Rho-asso
Afuresertib hydrochloride is an inhibitor of Akt kinase (Kis of 0.08/2/2.6 nM for Akt1/Akt2/Akt3 respectively)
价 格：￥电议型 号：T7885产 地：中国大陆
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T7829FK962Alzheimer,somatostatin,FK-962,FK 962,inhibit,FK962,Inhibitor,cognitive
FK962 is an somatostatin release enhancer , exerts cognitive-enhancing actions.
价 格：￥电议型 号：T7829产 地：中国大陆
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T19337GBR 12783 dihydrochloride
GBR 12783 dihydrochloride is a specific, potent and selective dopamine uptake inhibitor. GBR 12783 dihydrochloride inhibits the [3H]dopamine uptake by rat and mice striatal synaptosomes with IC50s of 1.8 nM and 1.2 nM, respectively.GBR 12783 dihydrochloride can improve memory performance and increase hippocampal acetylcholine release in rats.
价 格：￥电议型 号：T19337产 地：中国大陆
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TP1787LPKG Substrate acetate（81187-14-6 free base)PKG Substrate acetate（81187 14 6 free base),PKG Substrate
PKG Substrate acetate is a selective substrate for cGMP-dependent protein kinase (PKG).PKG Substrate is a selective substrate for protein kinase G (PKG) with a strong preference for PKG Iα (Km = 59 μM) over PKG II (Km = 305 μM).
价 格：￥电议型 号：TP1787L产 地：中国大陆
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T67882(2R,3S,11bS)-9,10-dimethoxy-3-(2-methylpropyl)-1H,2H,3H,4H,6H,7H,11bH-pyrido[2,1-a]isoquinolin-2-ol
(2R,3S,11bS)-9,10-dimethoxy-3-(2-methylpropyl)-1H,2H,3H,4H,6H,7H,11bH-pyrido[2,1-a]isoquinolin-2-ol is an impurity of Tetrabenazine, which is a VMAT inhibitor used in the treatment of hyperkinetic movement disorder.
价 格：￥电议型 号：T67882产 地：中国大陆
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T7845BTZO-1stress,inhibit,Cardiomyocyte,oxidative,Inhibitor,BTZO-1,Apoptosis,BTZO 1,BTZO1
BTZO-1 is an antioxidant response element (ARE) activator with cardioprotective activity.
价 格：￥电议型 号：T7845产 地：中国大陆
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T67783trans-isrib A17
trans-isrib A17 is an potent inhibitor of the integrated stress response with EC50 of 0.6 nM.
价 格：￥电议型 号：T67783产 地：中国大陆
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T7811Pilsicainide HClatrial tachyarrhythmias,SUN-1165,Pilsicainide HCl,antiarrhythmic,inhibit,orally acti
Pilsicainide HCl is a pure sodium channel blocker
价 格：￥电议型 号：T7811产 地：中国大陆
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T7858Ceftezole sodiumCTZ,Antibiotic,Ceftezole sodium,inhibit,Inhibitor,Bacterial,Ceftezole
Ceftezole sodium is a broad-spectrum cephalosporin antibiotic active gram-negative and gram-positive bacteria except for Proteus vulgaris, Pseudomonas aeruginosa, and Serratia marcescens. It has the inhibition of cell wall synthesis via affinity for penicillin-binding proteins. It also inhibits alpha-glucosidase.
价 格：￥电议型 号：T7858产 地：中国大陆
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TP1878LPACAP 1-38 acetatePACAP 138 acetate,PACAP 1 38 acetate
PACAP 1-38 acetate is a pituitary adenylate cyclase activating polypeptide (PACAP) analogue. PACAP 1-38 acetate binds to PACAP type I receptor(IC50 = 4 nM) and PACAP type II VIP2 receptor(IC50 = 1 nM) but not to PACAP type II, VIP1 receptor.
价 格：￥电议型 号：TP1878L产 地：中国大陆
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T8378AS2863619Cyclin dependent kinase,AS2863619,STAT,AS 2863619,Inhibitor,inhibit,CDK,AS-2863619
AS2863619 is an orally active inhibitor of cyclin-dependent kinase 8 (CDK8) and CDK19 (IC50s of 0.61 nM and 4.28 nM, respectively).
价 格：￥电议型 号：T8378产 地：中国大陆
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TP1430DTP3 TFA (1809784-29-9 free base)DTP3 TFA (1809784299 free base),DTP-3 TFA (1809784-29-9 free base),
DTP3 TFA is a potent and selective GADD45β/MKK7 (growth arrest and DNA-damage-inducible β/mitogen-activated protein kinase kinase 7) inhibitor.
价 格：￥电议型 号：TP1430产 地：中国大陆
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T67849O-Desethyl Dapagliflozin
O-Desethyl Dapagliflozin is a SGLT2 inhibitor, IC50=33nM.
价 格：￥电议型 号：T67849产 地：中国大陆
