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T9681MAK-683 hydrochlorideEED inhibitor,MAK 683 hyrochloride,embryonic ectoderm development,Histone Methy
MAK683 hydrochloride is an inhibitor of embryonic ectoderm development (EED) (patent US20160176882 A1, compound example 2). MAK683 exhibits IC50s of 59, 26, 89 nM in EED Alphascreen binding, ELISA and LC-MS assay.
价 格：￥电议型 号：T9681产 地：中国大陆
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TN6798Progoitringlucosinolate,inhibit,turnip family,thioglycoside,Progoitrin,Inhibitor,antithyroid activit
Progoitrin is a biochemical from the glucosinolate family that is found in some food, which is inactive but after ingestion is converted to goitrin. Goitrin decreases the thyroid hormone production. Apart from goitrin, progoitrin hydrolysis yields the nitrile, 1-cyano-2-hydroxy-3-butene (CHB), and the epithionitrile, 1-cyano-2-hydroxy-3,4-epithiobutane (CHEB).
价 格：￥电议型 号：TN6798产 地：中国大陆
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T21747VU0483605Inhibitor,inhibit,VU0483605,Metabotropic glutamate receptors,allosteric modulator,brain pen
VU0483605 is an effective and selective positive allosteric modulator of mGluR1 with EC50s of 390 and 356 nM for human and rat, respectively.
价 格：￥电议型 号：T21747产 地：中国大陆
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T6606NicaravenNicaraven,Inhibitor,inhibit
Nicaraven, a hydroxyl radical scavenger, has neuroprotective and antivasospastic effects.
价 格：￥电议型 号：T6606产 地：中国大陆
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T7730AminopterinAminopterin,tetrahydrofolic,inhibit,anticancer,immunosuppressive,acid,Antifolate,leukocyt
Aminopterin is a synthetic folic acid derivative whose metabolite is a competitive inhibitor of dihydrofolate reductase
价 格：￥电议型 号：T7730产 地：中国大陆
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TN6761Menthyl isovalerateMenthyl isovalerate
Menthyl isovalerate is a bioactive chemical.
价 格：￥电议型 号：TN6761产 地：中国大陆
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TP1555L1Fibronectin Active Fragment Control acetate
Fibronectin Active Fragment Control acetate is an active fragment of fibronectin which is a glycoprotein.
价 格：￥电议型 号：TP1555L1产 地：中国大陆
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TP17115-Tamra-DRVYIHP5 Tamra DRVYIHP,5TamraDRVYIHP
5-Tamra-DRVYIHP is a polypeptide containing rhodamine derivatives labeled with oligonucleotides.
价 格：￥电议型 号：TP1711产 地：中国大陆
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T7976Erythorbic Acidfood,Inhibitor,D-Isoascorbic acid,additive,inhibit,Erythorbic Acid,D-Araboascorbic ac
Erythorbic Acid is an antiscorbutic agent
价 格：￥电议型 号：T7976产 地：中国大陆
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T8506THPP-1PDE10A,SIMA,object,THPP 1,recognition,Phosphodiesterase (PDE),Inhibitor,inhibit,novel,THPP-1,T
THPP-1 is a potent and orally bioavailable inhibitor of PDE10A(Ki of 1 nM and 1.3 nM for human and rat PDE10A, respectively).
价 格：￥电议型 号：T8506产 地：中国大陆
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T6843GDC-0623Mitogen-activated protein kinase kinase,Apoptosis,inhibit,MEK,Inhibitor,MAP2K,MAPKK,MEK inhi
GDC-0623 is a potent and ATP-uncompetitive MEK1 inhibitor with Ki of 0.13 nM. Phase 1.
价 格：￥电议型 号：T6843产 地：中国大陆
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T91118-Azaadenosinethyroid,inhibit,editing,LIN28B,invasion,proliferation,Cal62,migration,8Azaadenosine,RN
8-Azaadenosine is a potent ADAR1 inhibitor and an A-to-I editing inhibitor. It blocks RNA editing and inhibits proliferation, 3D growth, invasion, and migration in thyroid cancer cells.
价 格：￥电议型 号：T9111产 地：中国大陆
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T9714Atpenin A5preconditioning,sensitive,mKATP,Atpenin A 5,Atpenin A5,ischemia,potassium,complex II,Inhib
Atpenin A5 is a potent and highly specific?complex II?inhibitor (IC50?~10 nM). Atpenin A5 is also an effective?mKATP?channel?agonist and cardioprotective agent[1].
价 格：￥电议型 号：T9714产 地：中国大陆
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T8235L-732138cytotoxicity,vagally-induced,NK receptor,Neurokinin Receptor,Inhibitor,ntravenously,lipopoly
L-732138 is a potent and competitive antagonist of neurokinin-1 (NK-1) receptor(IC50 : 2.3 nM)
价 格：￥电议型 号：T8235产 地：中国大陆
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T8254ChrysoobtusinInhibitor,Chrysoobtusin,derivative,anthraquinone,liver,inhibit
Chrysoobtusin belongs to the class of organic compounds known as hydroxyanthraquinones.
价 格：￥电议型 号：T8254产 地：中国大陆
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TN1040Skullcapflavone IIinhibit,inflammatory,Skullcapflavone II,Bacterial,antimicrobial,mycobacterial,diff
Skullcapflavone II is a flavonoid derived from Scutellaria baicalensis, a widely used herbal medicine in anti-inflammatory and anticancer therapy. Skullcapflavone II may have therapeutic potential for the treatment of allergic asthma.Skullcapflavone II regulates osteoclast differentiation, survival, and function. Skullcapflavone II exerts potent antimicrobial activity against M. aurum and M. bovis BCG
价 格：￥电议型 号：TN1040产 地：中国大陆
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T9672GRL-0496chloropyridyl,GRL-0496,3CLpro,inhibit,GRL0496,Inhibitor,SARS-CoV,GRL 0496,SARS coronavirus
GRL-0496 is a potent inhibitor with an enzyme inhibitory activity against SARS-CoV 3CLpro with an IC50 of 30 nM and antiviral potency with an EC50 value of 6.9 μM.
价 格：￥电议型 号：T9672产 地：中国大陆
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T9567Samatasvirinhibit,IDX18719,HCV,Samatasvir,IDX-719,infectious,IDX 719,IDX 18719,replication,antiviral
Samatasvir is a pan-genotypic inhibitor of the HCV non-structural protein 5A.
价 格：￥电议型 号：T9567产 地：中国大陆
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T6816DASA-58DASA58,inhibit,Inhibitor,DASA 58,DASA-58,glycolysis,TXNIP,cancer metabolism,Pyruvate Kinase,p
DASA-58 is a specific and potent Pyruvate kinase M2 (PKM2) activator.
价 格：￥电议型 号：T6816产 地：中国大陆
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T7752(S,R,S)-AHPC-MeVHL ligand-2,VHL ligand2,Inhibitor,inhibit,Ligands for E3 Ligase,(S,R,S) AHPC Me,(S,R
(S,R,S)-AHPC-Me (VHL ligand 2) is the (S,R,S)-AHPC-based VHL ligand used in the recruitment of the von Hippel-Lindau (VHL) protein[1]. (S,R,S)-AHPC-Me can be used to synthesize ARV-771. ARV-771 is a von Hippel-Landau (VHL) E3 ligase-based BET PROTAC degrader. ARV-771 potently degrades BET protein in castration-resistant prostate cancer (CRPC) cells with a DC50 <1 nM.
价 格：￥电议型 号：T7752产 地：中国大陆
