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T643433-Methylcarbazole
3-Methylcarbazole is an carbazole alkaloid compound with anticancer effects.
价 格：￥电议型 号：T64343产 地：中国大陆
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T64375UNC?1021UNC?1021
UNC 1021 is a selective L3MBTL3 inhibitor (IC50 = 0.048 μM).
价 格：￥电议型 号：T64375产 地：中国大陆
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T6437CefoperazoneCefoperazone,inhibit,Inhibitor,Antibiotic,Bacterial
Cefoperazone binds to and inactivates penicillin-binding proteins (PBPs) located on the inner membrane of the bacterial cell wall. PBPs are enzymes involved in the terminal stages of assembling the bacterial cell wall and in reshaping the cell wall during growth and division. Inactivation of PBPs interferes with the cross-linkage of peptidoglycan chains necessary for bacterial cell wall strength and rigidity. It can inhibit rMrp2-mediated [3H]E217βG uptake (IC50: 199 μM).
价 格：￥电议型 号：T6437产 地：中国大陆
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T10649c-Fms-IN-3c Fms IN 3,cFmsIN3
c-Fms-IN-3 is a novel inhibitor of the c-FMS and can be used in studies about antirheumatic and anti-inflammatory diseases.
价 格：￥电议型 号：T10649产 地：中国大陆
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TP1364LALX 40-4C acetateALX 404C acetate,ALX 40 4C acetate
ALX 40-4C acetate is a CXCR4 inhibitor of the chemokine receptor (Ki = 1 μM) and suppresses the replication of X4 strains of HIV-1. ALX 40-4C acetate is an antagonist of the APJ receptor (IC50 = 2.9 μM).
价 格：￥电议型 号：TP1364L产 地：中国大陆
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T643872-Nitrobenzoic acid
2-Nitrobenzoic acid is a antiproliferation agent. 2-Nitrobenzoic acid shows IC50 of 8.3 μM to jurkat cell line expressing T type calcium channel alpha 1H or its splice variant delta 25.
价 格：￥电议型 号：T64387产 地：中国大陆
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T9167PF-9363CTx-648,cancer,patient-derived,anti-tumor,HAT,CTx648,Inhibitor,HATs,selective,xenograft,CTx 6
PF-9363 is a potent and high selective KAT6A/KAT6B inhibitor. PF-9363 can be used for the research of cancer.
价 格：￥电议型 号：T9167产 地：中国大陆
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T6424Bromfenac SodiumInhibitor,inhibit,Bromfenac,Cyclooxygenase,HLEC-B3,Bromfenac Sodium,COX,ocular infla
Bromfenac Sodium is a nonsteroidal anti-inflammatory drug (NSAID), which has anti-inflammatory activity and may block prostaglandin synthesis by inhibiting cyclooxygenase 1 and 2.
价 格：￥电议型 号：T6424产 地：中国大陆
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T6410Bexarotenecutaneous,lymphoma,selective,?retinoid,inhibit,Retinoic acid receptors,antineoplastic,T-ce
Bexarotene is a retinoid analogue that is used to treat the skin manifestations of cutaneous T cell lymphoma (CTCL).
价 格：￥电议型 号：T6410产 地：中国大陆
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T6557KU-0060648mTOR,inhibit,KU-0060648,Phosphoinositide 3-kinase,Inhibitor,Mammalian target of Rapamycin,
KU-0060648 is a dual inhibitor of DNA-PK and PI3Kα, PI3Kβ, PI3Kδ with IC50 of 8.6 nM and 4 nM, 0.5 nM, 0.1 nM respectively, less inhibition of PI3Kγ with IC50 of 0.59 μM.
价 格：￥电议型 号：T6557产 地：中国大陆
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T64354Cystathionine-γ-lyase-IN-1
Cystathionine-γ-lyase-IN-1 is a selective inhibitor of cystathionine γ-lyase (CSE) enzyme (IC50= 6.3 μM).
价 格：￥电议型 号：T64354产 地：中国大陆
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T6499Fenticonazole Nitrateinhibit,Fenticonazole,Fenticonazole Nitrate,Antibiotic,Fungal,Inhibitor
Fenticonazole Nitrate is an azole agent with antifungal activity.
价 格：￥电议型 号：T6499产 地：中国大陆
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T7964Isomaltoral,food,stabilizing,Inhibitor,Lactate Dehydrogenase,inhibit,agent,LDH,Isomalt,industry,exci
Palatinitol is a mixture of 1,6-mannitol glucopyranoside and 1,6-sorbitol glucopyranoside
价 格：￥电议型 号：T7964产 地：中国大陆
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T6446ClevudineOrthopoxvirus,half-life,nucleoside,DNA/RNA Synthesis,analog,Inhibitor,polymerase,Hepatitis
Clevudine is a synthetic pyrimidine analogue with activity against hepatitis B virus (HBV). Intracellularly, clevudine is phosphorylated to its active metabolites, clevudine monophosphate and triphosphate. The triphosphate metabolite competes with thymidine for incorporation into viral DNA, thereby causing DNA chain termination and inhibiting the function of HBV DNA polymerase (reverse transcriptase). Clevudine has a long half-life and shows significant reduction of covalently closed circular DN
价 格：￥电议型 号：T6446产 地：中国大陆
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T86486-AZATHYMINE6-Azathymine,6AZATHYMINE,antibacterial,nucleobase,Inhibitor,Influenza Virus,DNA,6-nitrog
6-azathymine is a potent inhibitors of D-3-aminoisobutyrate-pyruvate aminotransferase. 6-Azauracil acted as a competitive inhibitor with respect to beta-alanine, and was an uncompetitive inhibitor with respect to pyruvic acid with a Ki of approximately 8.9 mM.
价 格：￥电议型 号：T8648产 地：中国大陆
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T7364NNC-0640NNC-0640,Glucagon Receptor,NNC0640,GCGR,inhibit,Inhibitor,NNC 0640
NNC-0640 is a negative allosteric modulator of Human Glucagon Receptor with an IC50 of 69.2 nM.
价 格：￥电议型 号：T7364产 地：中国大陆
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T64337PF-04745637PF04745637,Inhibitor,bowel,TRPA1,disease,inhibit,respiratory,PF-04745637,Transient recept
PF-04745637 is a potent and selective TRPA1 antagonist with an IC50 of 17 nM[1].
价 格：￥电议型 号：T64337产 地：中国大陆
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T6422Brimonidine TartrateUK-14304,UK14304,AGN190342,Brimonidine,Adrenergic Receptor,AGN-190342,AGN 190342
Brimonidine tartrate is a quinoxaline derivative and adrenergic α-2 receptor agonist (EC50: 0.45 nM) that is used to manage intraocular pressure associated with open-angle glaucoma or ocular hypertension.
价 格：￥电议型 号：T6422产 地：中国大陆
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TP1875LCDK2 acetate(255064-79-0 free base)CDK2 acetate(255064790 free base),CDK-2 acetate(255064-79-0 free
CDK2 acetate is a member of the eukaryotic S/T protein kinase family and its function is to catalyze the phosphoryl transfer of ATP γ-phosphate to serine or threonine hydroxyl (denoted as S0/T0) in a protein substrate.
价 格：￥电议型 号：TP1875L产 地：中国大陆
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T6450ClinofibrateClinofibrate,HMG-CoA Reductase (HMGCR),Autophagy,inhibit,Inhibitor,S 8527,S8527
Clinofibrate（IC50 of 0.47 mM）, a lipid-lowering agent, inhibits hydroxymethylglutaryl coenzyme A reductase (HMGCR). It is utilized to control high cholesterol and triacylglyceride levels in the blood.
价 格：￥电议型 号：T6450产 地：中国大陆
