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T14345Atropine methyl bromideAtropine methyl bromide,Methylatropine bromide,
Atropine methyl bromide, a muscarinic receptor (mAChR) antagonist. Which is a quaternary ammonium salt of atropine and a mydriatic for dilation of the pupil during ophthalmic examination. It penetrates less readily into the central nervous system than atr
价 格：￥电议型 号：T14345产 地：美洲
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T14347AureothricinAureothricin
Aureothricin is a dithiolopyrrolone (DTP) antibiotic first isolated from Streptomyces and exhibits relatively broad-spectrum antibiotic activity, and it also can inhibit adhesion of human umbilical vein endothelial cells (HUVECs) to vitronectin[1].
价 格：￥电议型 号：T14347产 地：美洲
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T14348Auristatin EAuristatin E
Auristatin E inhibits cell division by blocking the polymerisation of tubulin. Auristatin E is a cytotoxic tubulin modifier with potent and selective antitumor activity; MMAE analog and cytotoxin in Antibody-drug conjugates.
价 格：￥电议型 号：T14348产 地：美洲
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T14349Auristatin FAuristatin F
Auristatin F is a potent cytotoxin. Auristatin F, a potent microtubule inhibitor and vascular damaging agent (VDA). Which can be used in antibody-drug conjugates (ADC)[1].
价 格：￥电议型 号：T14349产 地：美洲
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T1435PraziquantelPraziquantel,Droncit,Biltricide
Praziquantel increases the permeability of the tegument of susceptible worms, resulting in an influx and increase in intra-tegumental calcium leading to rapid contractions and paralysis of the worm´s musculature through a subsequent increase in levels of
价 格：￥电议型 号：T1435产 地：美洲
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T14350SoblidotinSoblidotin,Auristatin PE,TZT-1027
Soblidotin (Auristatin PE) is an inhibitor of tubulin polymerization. It also is a novel synthetic Dolastatin 10 derivative.
价 格：￥电议型 号：T14350产 地：美洲
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T14351AurothioglucoseAurothioglucose,Gold thioglucose,
Aurothioglucose (Gold thioglucose) is a well known active-site inhibitor of TrxR1. Which inhibited TrxR1 activity in HeLa cell cytosol but had no effect on the viability of the cells. IC50 value: Target: TrxR1 in vitro: Trx1 redox state and ROS generation
价 格：￥电议型 号：T14351产 地：美洲
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T14353AuxinoleAuxinole
Auxinole is a potent auxin antagonist of TIR1/AFB receptors, binding TIR1 to block the formation of the TIR1-IAA-Aux/IAA complex .so it inhibits auxin-responsive gene expression.
价 格：￥电议型 号：T14353产 地：美洲
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T14354AVE 0991 sodium saltAVE 0991 sodium salt
AVE 0991 competes for high-affinity binding of [125I]-Ang-(1-7) to bovine aortic endothelial cell membranes, with IC50 of 21±35 nM. AVE 0991 sodium salt is a nonpeptide and orally active Ang-(1-7) receptor Mas agonist.
价 格：￥电议型 号：T14354产 地：美洲
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T14355AVE-3085AVE-3085
AVE-3085 is a potent endothelial nitric oxide synthase enhancer. Which is used for cardiovascular disease treatment.
价 格：￥电议型 号：T14355产 地：美洲
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T14358AvoralstatAvoralstat,BCX4161,
Avoralstat is an oral plasma kallikrein (PKK) inhibitor. Which is used for the treatment of hereditary angioedema.
价 格：￥电议型 号：T14358产 地：美洲
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T14364-Aminohippuric Acid4-Aminohippuric Acid,p-Aminohippuric acid,
Aminohippuric acid is the glycine amide of 4-aminobenzoic acid. Its sodium salt is used as a diagnostic aid to measure effective renal plasma flow (ERPF) and excretory capacity.
价 格：￥电议型 号：T1436产 地：美洲
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T14362AY 9944AY 9944
AY 9944 is a specific cholesterol biosynthesis inhibitor. AY 9944 inhibits the 7-dehydro cholesterol Δ7-reductase (DHCR7) enzyme (IC50=13 nM). At high doses, AY 9944 inhibits also in cultured embryos sterol Δ7-Δ8 isomerase, which causes the accumulation o
价 格：￥电议型 号：T14362产 地：美洲
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T14363AZ-23AZ-23,AZ23,AZ 23
AZ-23 is an inhibitor of ATP-competitive and Trk kinase A/B/C. For TrkA, TrkB, FGFR1, Flt3, Ret, MuSk, Lck, the IC50s values are 2 nM, 8 nM, 24 nM, 52 nM, 55 nM, 84 nM, 99 nM, respectively.
价 格：￥电议型 号：T14363产 地：美洲
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T14364AZ-Dyrk1B-33AZ-Dyrk1B-33
AZ-Dyrk1B-33 is a potent and selective Dyrk1B kinase inhibitor. With an IC50 of 7 nM[1].
价 格：￥电议型 号：T14364产 地：美洲
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T14365AZ PFKFB3 26AZ PFKFB3 26
AZ PFKFB3 26 inhibits PFKFB1 and PFKFB2 with IC50s of 2.06 and 0.384 μM, respectively[1]. AZ PFKFB3 26 is a potent and selective inhibitor of the metabolic kinase PFKFB3 with an IC50 of 23 nM.
价 格：￥电议型 号：T14365产 地：美洲
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T14367AZ1495AZ1495
AZ1495 (compound 28) is an oral active inhibitor of Interleukin-1 receptor associated kinase 4 (IRAK4), with IC50 values of 5 nM and 23 nM for IRAK4 and IRAK1, respectively. Which Shows activity in treatment of mutant MYD88L265P diffuse large B-cell lymph
价 格：￥电议型 号：T14367产 地：美洲
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T14369AZD-0284AZD-0284
AZD-0284 is an inverse agonist of the nuclear receptor RORγ. In development for the treatment of plaque psoriasis vulgaris and respiratory tract disorders[1].
价 格：￥电议型 号：T14369产 地：美洲
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T1437DexpanthenolDexpanthenol,D-Panthenol,Pantothenol
Dexpanthenol is an alcoholic analogue of D-pantothenic acid and cholinergic agent. Dexpanthenol acts as a precursor of coenzyme A necessary for acetylation reactions and is involved in the synthesis of acetylcholine. Although the exact mechanism of the ac
价 格：￥电议型 号：T1437产 地：美洲
