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T22466Adenosine receptor A1 antagonist 5；化合物 Adenosine receptor A1 antagonist 5Adenosine receptor A1 antag
Adenosine receptor A1 antagonist 5 acts as an adenosine antagonist, is an oxypurine, acts as an insecticide and pest control agent, and has an inhibitory effect on elevated blood pressure.
价 格：￥电议型 号：T22466产 地：中国大陆
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T224651,2-Distearoyl-sn-glycerol；(2S)-3-羟基-1,2-丙烷二基二硬脂酸酯1,2-Distearoyl-sn-glycerol
1,2-Distearoyl-sn-glycerol is an internal standard for the isolation and characterization of molecular species of 1,2-diacyl-sn-glycerol (DAG).
价 格：￥电议型 号：T22465产 地：中国大陆
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T224641,2-Dimyristoyl-sn-glycerol；1,2-二肉豆蔻酸甘油酯1,2-DMG；1,2-DMG|||1,2-二肉豆蔻酸甘油酯
1,2-Dimyristoyl-sn-glycerol (1,2-DMG) is able to increase AChE activity by 35-40% at concentrations of 25 micrograms/ml in the parasite S. mansoni..
价 格：￥电议型 号：T22464产 地：中国大陆
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T224631,2-Dilauroyl-sn-glycerol；1,2-二月桂酰-SN-甘油1,2-DLG|||(S)-1,2-Dilaurin；1,2-DLG|||(S)-1,2-Dilaurin|||1,2-
1,2-Dilauroyl-sn-glycerol ((S)-1,2-Dilaurin) is primarily composed of the interaction of 1,2-dilauroyl-sn-glycerol (1,2-DLG) with phosphatidylcholine (PC) bilayers.
价 格：￥电议型 号：T22463产 地：中国大陆
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T224621,2,3,4,5,6-Hexabromocyclohexane；化合物 T224621,2,3,4,5,6-Hexabromocyclohexane
The compound effectively and directly inhibits JAK2 tyrosine kinase autophosphorylation and specifically inhibits ligand-dependent JAK2 activation. It has no cytotoxicity at 100 μM. A 16-hour treatment with compound (1 μM) decreases JAK2 tyrosine autophosphorylation levels to ~ 50% while 50 μM eliminates nearly all JAK2 activity.
价 格：￥电议型 号：T22462产 地：中国大陆
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T22461YKL-5-124；化合物YKL-5-124YKL-5-124
YKL-5-124, a potent, selective and covalent CDK7 inhibitor with an IC50 of 9.7 nM, 1300 nM and 3020 nM for CDK7/Mat1/CycH, CDK2 and CDK9 respectively, displays biochemical and cellular selectivity for CDK7 over CDK12/13.
价 格：￥电议型 号：T22461产 地：中国大陆
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T22460XMD-17-51；化合物XMD-17-51XMD17-51；XMD17-51
XMD-17-51 is a potent and highly selective NUAK1 inhibitor.
价 格：￥电议型 号：T22460产 地：中国大陆
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T2246LRRK2-IN-1化合物LRRK2-IN-15,11-二氢-2-[[2-甲氧基-4-[[4-(4-甲基-1-哌嗪基)-1-哌啶基]羰基]苯基]氨基]-5,11-二甲基-6H-嘧啶并[4,5-B][1
LRRK2-IN-1 is an effective and selective LRRK2 inhibitor.
价 格：￥电议型 号：T2246产 地：中国大陆
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T22459Xanthinol Nicotinate；烟酸占替诺Angioamin|||Complamin；Angioamin|||烟酸占替诺|||Complamin
Xanthinol Nicotinate (Complamin) is a potent vasodilator that can easily enter the cell and causes an increase in glucose metabolism resulting in an increased energy.
价 格：￥电议型 号：T22459产 地：中国大陆
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T22458WEHL-04；7-溴-1,2,3,4-四氢喹啉7-Bromo-1,2,3,4-tetrahydroquinoline；7-Bromo-1,2,3,4-tetrahydroquinoline|||7-
WEHL-04 is an intermediate used to prepare (isoquinolinylsulfonyl)benzoic acids as inhibitors of type 5 71-β-hydroxysteroid dehydrogenase AKR1C3. It is also used in the synthesis of 2-aminooctahydrocyclopentalene-3a-carboxamides as potent CCR2 antagonists.
价 格：￥电议型 号：T22458产 地：中国大陆
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T22457WEHL-03；4-氨基-3-氰基-1,2,5,6-四氢吡啶4-AMINO-3-CYANO-1,2,5,6-TETRAHYDROPYRIDINE；4-AMINO-3-CYANO-1,2,5,6-TET
WEHL-03 (4-AMINO-3-CYANO-1,2,5,6-TETRAHYDROPYRIDINE) is an active chemical.
价 格：￥电议型 号：T22457产 地：中国大陆
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T22456Voreloxin hydrochloride；化合物Voreloxin hydrochlorideSNS-595 hydrochloride|||Vosaroxin；SNS-595 hydrochl
Voreloxin hydrochloride (SNS-595 hydrochloride) is a potent inhibitor of Topoisomerase II with broad-spectrum anti-tumor activity.
价 格：￥电议型 号：T22456产 地：中国大陆
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T22455Vindesine sulfate；硫酸长春地辛DVA|||Desacetylvinblastine amide|||DAVA|||Desacetyl Vinblastine amide|||VDS；
Vindesine sulfate (Desacetyl Vinblastine amide) is a vinca alkaloid which is a synthetic derivative of vinblastine, binds to the microtubular proteins of the mitotic spindle, leading to crystallization of the microtubule and mitotic arrest or cell death.
价 格：￥电议型 号：T22455产 地：中国大陆
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T22454Vidarabine monohydrate维达拉滨一水合物维达拉滨一水合物|||Vira-A monohydrate|||Spongoadenosine monohydrate|||阿糖腺苷一水合物
Vidarabine, a nucleoside antibiotic with antiviral acitivity that interferes with the synthesis of viral DNA, is used to treat varicella zoster and herpes simplex viruses.
价 格：￥电议型 号：T22454产 地：中国大陆
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T22453Venlafaxine；文拉法辛Wy 45030；Wy 45030|||文拉法辛
Venlafaxine (Wy 45030), an arylalkanolamine serotonin-norepinephrine reuptake inhibitor (SNRI), is used to treat major generalised anxiety disorder (GAD), depressive disorder (MDD), panic disorder and social phobia.
价 格：￥电议型 号：T22453产 地：中国大陆
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T22452Valbenazine tosylate；結苯那嗪NBI-98854；結苯那嗪|||NBI-98854
Valbenazine tosylate, the tosylate salt of valbenazine, is a vesicular monoamine transporter 2 (VMAT2) inhibitor with a Ki value of 150 nM while displaying no significant binding to VAMT1(Ki<10 μM).
价 格：￥电议型 号：T22452产 地：中国大陆
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T22451UK-371804 HCl化合物UK-371804 HClUK 371804 HCl|||UK371804 HCl
UK-371804 is a potent and selective urokinase-type plasmogen activator (uPA) inhibitor with excellent enzyme potency (Ki=10 nM) and selectivity profile (2700-fold versus plasmin and 4000-fold versus tPA).
价 格：￥电议型 号：T22451产 地：中国大陆
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T22450Tyrphostin B44, (+) enantiomer酪氨酸磷酸化抑制剂AG 835酪氨酸磷酸化抑制剂AG 835
Tyrphostin B44, (+) enantiomer is an inhibitor of epidermal growth factor receptor (EGFR) kinase with IC50 of 0.86 μM and has less active than the (-) enantiomer.
价 格：￥电议型 号：T22450产 地：中国大陆
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T2245CL-387785；化合物CL-387785WAY-EKI 785|||EKI-785；WAY-EKI 785|||EKI-785
CL-387785 (WAY-EKI 785)(EKI785; WAY-EKI 785) is an irreversible inhibitor of EGFR(IC50： 370+/-120 pM); is able to overcome resistance caused by the T790M mutation on a functional level.
价 格：￥电议型 号：T2245产 地：中国大陆
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T22449Tubastatin A TFA化合物Tubastatin A TFATubastatin A trifluoroacetate salt
Tubastatin A is a potent HDAC6 inhibitor with IC50 of 15 nM.
价 格：￥电议型 号：T22449产 地：中国大陆
