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产品数：86101
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T8439Clobenpropit dihydrobromideApoptosis,inhibit,Clobenpropit dihydrobromide,histamine H3R,antagonist,in
Clobenpropit dihydrobromide is a potent antagonist and inverse agonist of histamine H3R (histamine H3LR,pEC50 of 8.07)
价 格：￥电议型 号：T8439产 地：中国大陆
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T8796CAN508inhibit,CAN 508,ATP-competitive,Cyclin dependent kinase,esophageal,cells,CDK,CAN508,Inhibitor,
CAN508 is a potent, ATP-competitive CDK9/cyclin T1 inhibitor with an IC50 of 0.35 μM. It is also a competitive inhibitor of Cdk2-cyclin E with respect to ATP, with Ki and IC50 values of 13.3 and 20 μM, respectively.CAN508 exhibits a 38-fold selectivity for CDK9/cyclin T over other CDK/cyclin complexes. Antitumor activity.
价 格：￥电议型 号：T8796产 地：中国大陆
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TP1545L1FFAGLDD amine saltFFAGLDD amine salt
FFAGLDD amine salt is MMP9 selective cleavage peptides, which used for cytosolic delivery of Doxorubi-cin (DOX) and achieve temporally and spatially controlled slow drug delivery and release.
价 格：￥电议型 号：TP1545L1产 地：中国大陆
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T38163ML-148ML-148,ML 148,selective,Inhibitor,prostaglandin-signaling,15-PGDH,15-Hydroxyprostaglandin dehy
ML-148 is a selective inhibitor of 15-hydroxy prostaglandin dehydrogenase (15-PGDH, IC50 = 56 nM). ML-148 can be used to profile across a panel of related dehydrogenase or reductase enzymes and in studies about prostaglandin-signaling pathways.
价 格：￥电议型 号：T38163产 地：中国大陆
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T9374AA38-3serine,ABHD6,Fatty acid amide hydrolase,AA38 3,Monoacylglycerol lipase,AA383,ABHD11,FAAH,MAGL,
AA38-3 inhibites three SHs (ABHD6, ABHD11, and FAAH)
价 格：￥电议型 号：T9374产 地：中国大陆
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T10889CRTh2 antagonist 2CRTh2 antagonist 2,CRTh-2 antagonist 2
CRTh2 antagonist 2 is a selective and potent CRTH2 antagonist, IC50≤10 nM. CRTh2 antagonist 2 can be used to study the direction of androgenic alopecia.
价 格：￥电议型 号：T10889产 地：中国大陆
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TN1482Chamaechromonehepatitis B,HBsAg,anti-HBV,Stellera chamaejasme L,HBV,inhibit,virus,Chamaechromone,Inh
Chamaechromone is a natural product isolated from the roots of Stellera chamaejasme L.. Chamaechromone has anti-HBV and insecticidal activity.
价 格：￥电议型 号：TN1482产 地：中国大陆
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T6S1683DemethoxycurcuminBacterial,Inhibitor,Autophagy,Demethoxycurcumin,inhibit,Apoptosis
1. Demethoxycurcumin has antioxidant activity. 2. Demethoxycurcumin has anti-inflammatory activity. 3. Demethoxycurcumin has anti-proliferative activity. 4. Demethoxycurcumin has anti-acanthamoebic effect. 5. Demethoxycurcumin is a potential additive natural product in combination with chemotherapeutic agents in drug-resistant cancers. 6. Demethoxycurcumin inhibits energy metabolic and oncogenic signaling pathways through AMPK activation in triple-negative breast cancer cells.
价 格：￥电议型 号：T6S1683产 地：中国大陆
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T9975GPR183GPR183 antagonist-1,SAE-14,inhibit,SAE 14,SAE14,HL-60,GPR183,Inhibitor,GPR183 antagonist SAE-1
GPR183 is a chemotactic receptor known for its role in the maturation of B cells, and the endogenous ligand is the oxysterol 7α,25-dihydroxycholesterol (7α,25-OHC). GPR183 can be used in research on inflammatory bowel disease (IBD).
价 格：￥电议型 号：T9975产 地：中国大陆
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T6952Prasugrel HydrochloridePCR4099,aggregation,platelet,Inhibitor,P2Y Receptor,antiplatelet,ADP,active,P
Prasugrel hydrochloride is a piperazine derivative and pletelet aggregation inhibitor that is used to prevent thrombosis in patients with acute coronary syndrome.
价 格：￥电议型 号：T6952产 地：中国大陆
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T10269AHR antagonist 2AHR antagonist 2
AHR antagonist 2 is an antagonist of the aryl hydrocarbon receptor. The IC50s for human AHR and mouse AHR are 0.885 and 2.03 nM, respectively.
价 格：￥电议型 号：T10269产 地：中国大陆
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T6841FumagillinFumagillin,NSC 9168,Antibiotic,inhibit,Human immunodeficiency virus,Parasite,Inhibitor,NSC
Fumagillin is a selective and potent irreversible inhibitor of Methionine aminopeptidase 2 (MetAP2), used as an antibiotic to treat microsporidiosis.
价 格：￥电议型 号：T6841产 地：中国大陆
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T8320J14cancer,inhibit,damage,Sulfiredoxin,J14,cytotoxicity,Reactive Oxygen Species,J 14,death,adenocarci
J-14 is an inhibitor of reversible sulfiredoxin(IC50 : 8.1 μM). J14 induces oxidative stress (intracellular ROS accumulation) by inhibiting sulfiredoxin, leading to cytotoxicity and cancer cell death
价 格：￥电议型 号：T8320产 地：中国大陆
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T6S0105PeiminineInhibitor,inhibit,Peiminine,Autophagy
1. Peiminine is an effective inhibitor for lung inflammation and pulmonary fibrosis in a rat model of bleomycin-induced lung injury.
价 格：￥电议型 号：T6S0105产 地：中国大陆
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TQ0187SR-3677Inhibitor,Rho-associated protein kinase,Autophagy,SR 3677,Rho-kinase,SR3677,ROCK,ROK,SR-3677,
SR-3677 is an effective and specific inhibitor of ROCK2 (IC50: 3 nM).
价 格：￥电议型 号：TQ0187产 地：中国大陆
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TN6732Oenothein Bantitumor,HCV,Hepatitis C virus,ellagitannin,antifungal,antioxidant,Bacterial,inhibit,Oen
Oenothein B is a specific inhibitor of poly(ADP-ribose) glycohydrolase. Oenothein B shows antioxidant, anti-inflammatory, antifungal, anti-HCV, and antitumor properties.
价 格：￥电议型 号：TN6732产 地：中国大陆
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T9459GR103545Inhibitor,Opioid Receptor,imaging,GR103545,inhibit,κ-OR,GR 103545,κ-opioid receptor,GR-10354
(R)-(-)-GR103545 fumarate is a chemical compound.
价 格：￥电议型 号：T9459产 地：中国大陆
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T63812MrgprX2 antagonist-8
MrgprX2 antagonist-8 is an MrgprX2 antagonist that can be used to study inflammatory diseases.
价 格：￥电议型 号：T63812产 地：中国大陆
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T61972Pomaglumetad methionil hydrochloride
Pomaglumetad methionine hydrochloride (LY2140023 hydrochloride) is a methionine prodrug of LY404039 with oral activity. LY404039 is a selective mGlu2/3 receptor agonist. Pomaglumetad methionil hydrochloride has research value in schizophrenia.
价 格：￥电议型 号：T61972产 地：中国大陆
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T7015Vps34-IN-1inhibit,Autophagy,Vps34IN1,PI3K,Vps-34-IN-1,Inhibitor,Phosphoinositide 3-kinase,Vps34 IN 1
Vps34-IN1 is a potent and highly selective Vps34 inhibitor with IC50 of 25 nM invitro, which does not significantly inhibit the isoforms of class I as well as class II PI3Ks.
价 格：￥电议型 号：T7015产 地：中国大陆
