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T6481DroxinostatHDAC3,hepatocellular carcinoma (HCC),Droxinostat,NS-41080,Apoptosis,Histone deacetylases,
Droxinostat is a selective inhibitor of HDAC, mostly for HDACs 6 and 8 with IC50 of 2.47 μM and 1.46 μM, greater than 8-fold selective against HDAC3 and no inhibition to HDAC1, 2, 4, 5, 7, 9, and 10.
价 格：￥电议型 号：T6481产 地：中国大陆
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T7357(S)-b-aminoisobutyric acidEndogenous Metabolite,Inhibitor,inhibit,(S) b aminoisobutyric acid,(S)bami
(S)-b-aminoisobutyric acid is a non-protein amino acid originating from the catabolism of valine and thymine.
价 格：￥电议型 号：T7357产 地：中国大陆
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T21714BMS453Inhibitor,BMS453,retinoid,RAR/RXR,inhibit,BMS-453,BMS 189453,TGFβ,breast,RARβ,RARγ,Retinoid X
BMS453, a synthetic retinoid, is a potent and selective agonist of RARβ and a potent testicular toxin. BMS453 inhibits breast cell growth predominantly through the induction of active TGFβ.
价 格：￥电议型 号：T21714产 地：中国大陆
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T9461AZ194nociceptive neurotransmission,Inhibitor,CRMP2-Ubc9 interaction,Na+ channels,Na channels,inhibit
CRMP2-Ubc9-NaV1.7 inhibitor 194, is a CRMP2-Ubc9-NaV1.7 inhibitor.
价 格：￥电议型 号：T9461产 地：中国大陆
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T23445Anxiolytic/nonsedative agent-1
Anxiolytic/nonsedative agent-1 is a potent and selective GABAA agonist. Anxiolytic/nonsedative agent-1 shows appreciable affinity for the BzR in bovine brain membranes with Kis of 14, 121, 239 nM for α1β2γ2, α2β2γ2, α5β3γ2, respectively. Anxiolytic/nonsedative agent-1 shows α2 selective efficacy in vitro and anxioselective effects in vivo.
价 格：￥电议型 号：T23445产 地：中国大陆
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T7891IpidacrineIpidacrine,inhibit,cholinesterase,nootropic,Inhibitor,Cholinesterase (ChE),Alzheimer disea
Ipidacrine (NIK‐247) is an Antidementia Agent
价 格：￥电议型 号：T7891产 地：中国大陆
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T7167Purvalanol BPurvalanol B,cdc2,inhibit,cyclin,CDK2,CDK5,CDK,Parasite,P. falciparum,ATP,NG95,Cyclin de
Purvalanol B is a CDK inhibitor that inhibits Cdk2/cyclin A, Cdk2/cyclin E, Cdk5/p35, and Cdk2/cyclin B (IC50s = 6, 9, 6, and 6 nM, respectively)
价 格：￥电议型 号：T7167产 地：中国大陆
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T7305JQEZ5S-adenosyl,EZH2,JQEZ5,antitumor,methionine,JQEZ 5,H3K27me3,PRC2,inhibit,Inhibitor,JQEZ-5,Histon
JQEZ5 is an inhibitor of EZH2 lysine methyltransferase (IC50 = 11.1 nM).
价 格：￥电议型 号：T7305产 地：中国大陆
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T6737ZaltoprofenCN-100,anti-inflammatory,COX-2,inhibit,non-steroidal,Zaltoprofen,Inhibitor,COX,NSAID,COX-
Zaltoprofen is a Cox-1 and Cox-2 inhibitor, which is used for the treatment of arthritis.
价 格：￥电议型 号：T6737产 地：中国大陆
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T8238Fosamprenavir Calcium SaltHuman immunodeficiency virus,HIV,Fosamprenavir Calcium Salt,Inhibitor,inhi
Fosamprenavir Calcium Salt (GW433908G) is a phosphate ester prodrug of the antiretroviral protease inhibitor Amprenavir, with improved solubility. Fosamprenavir Calcium Salt has Anti-HIV infection.
价 格：￥电议型 号：T8238产 地：中国大陆
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TN12132-(Hydroxymethyl)anthraquinonesex pheromone,inhibit,2(Hydroxymethyl)anthraquinone,2 (Hydroxymethyl)a
2-(Hydroxymethyl)anthraquinone exhibits strong activity against Helicobacter pylori ATCC 43504 at 0.01 mg/disc.
价 格：￥电议型 号：TN1213产 地：中国大陆
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T8175DL-LaudanosineDrug Metabolite,DLLaudanosine,DL Laudanosine,DL-Laudanosine,Inhibitor,inhibit
Laudanosine is a recognized metabolite of atracurium and cisatracurium.
价 格：￥电议型 号：T8175产 地：中国大陆
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T7393ONO-7300243ONO7300243,inhibit,Inhibitor,ONO 7300243,ONO-7300243,LPL Receptor,Lysophospholipid Recept
ONO-7300243 is an antagonist of lysophosphatidic acid receptor 1 (LPA1; IC50 : 0.16 μM).
价 格：￥电议型 号：T7393产 地：中国大陆
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T36640Xanomeline
Xanomeline is a functionally selective M1/M4 activator used in the study of neurological disorders such as schizophrenia and has shown promising treatment in preclinical trials. Xanomeline is well absorbed orally, crosses the blood-brain barrier and undergoes extensive liver metabolism with at least six metabolites.
价 格：￥电议型 号：T36640产 地：中国大陆
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TN1480CephaelineNSC 32944,inhibit,Inhibitor,NSC32944,Ebola,Cephaeline,Filovirus,phenolic,alkaloid,virus,In
Cephaeline was highly active against protected primary CLL cells (relative IC50´s 35nM ) and acted by repressing HIF-1α± and disturbing intracellular redox homeostasis.
价 格：￥电议型 号：TN1480产 地：中国大陆
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T22286Cyanosafracin Binhibit,Inhibitor,Cyanosafracin B
Cyanosafracin B is a compound which can be used in the synthesis of ecteinascidin ET-743 (an antitumor chemotherapy drug).
价 格：￥电议型 号：T22286产 地：中国大陆
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T8875CD73-IN-3Inhibitor,cancer,CD73 IN 3,CD-73-IN-3,CD73IN3,CD73,Immunosuppression,tumor,inhibit
LY-3475070 is a potent and selective CD73 inhibitor with an IC50 of 28 nM, and its use alone or in combination with pembrolizumab is currently being tested in patients with advanced cancer.
价 格：￥电议型 号：T8875产 地：中国大陆
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T9493DL-2-AMINOOCTANOIC ACIDDL2AMINOOCTANOIC ACID,DL 2 AMINOOCTANOIC ACID
DL-2-Aminooctanoic acid, also known as a-aminocaprylate or alpha-aminocaprylic acid, belongs to the class of organic compounds known as alpha-amino acids.
价 格：￥电议型 号：T9493产 地：中国大陆
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T9289Phosphonoformic acid trisodium salt hexaPhosphonoformic acid trisodium salt hexa
Phosphonoformic acid trisodium salt hexa is an antiviral drug for the treatment of CMV retinitis.
价 格：￥电议型 号：T9289产 地：中国大陆
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T7523Guanidinosuccinic acidInhibitor,Endogenous Metabolite,Guanidinosuccinic acid,inhibit
Guanidinosuccinic acid (GSA) has been identified as a uremic toxin, is a nitrogenous metabolite isolated in excess from serum and urine.
价 格：￥电议型 号：T7523产 地：中国大陆
