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T1301517-Hydroxy--costic acid；化合物 7-Hydroxy--costic acid7-Hydroxy--costic acid
7-Hydroxy--costic acid is a useful organic compound for research related to life sciences and the catalog number is T130151.
价 格：￥电议型 号：T130151产 地：中国大陆
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T130051Detigloylswietenine, 2-Hydroxy, 8?,30?-epoxide, 3-；化合物 Detigloylswietenine, 2-Hydroxy, 8?,30?-epoxid
Detigloylswietenine, 2-Hydroxy, 8?,30?-epoxide, 3- is a useful organic compound for research related to life sciences and the catalog number is T130051.
价 格：￥电议型 号：T130051产 地：中国大陆
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T129516Formononetin, 7-O-[?-D-Apiofuranosyl-(1?6)-?-D-glu；化合物 Formononetin, 7-O-[?-D-Apiofuranosyl-(1?6)-?-
Formononetin, 7-O-[?-D-Apiofuranosyl-(1?6)-?-D-glu is a useful organic compound for research related to life sciences and the catalog number is T129516.
价 格：￥电议型 号：T129516产 地：中国大陆
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T12951Sodium Channel inhibitor 2；化合物 T12951Sodium Channel inhibitor 2
Sodium Channel inhibitor 2 is a blocker of sodium channel.
价 格：￥电议型 号：T12951产 地：中国大陆
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T12925Sitravatinib malate；化合物 T12925MGCD516 malate|||MG-516 malate；MGCD516 malate|||MG-516 malate
Sitravatinib malate is an orally bioavailable receptor inhibitor of tyrosine kinase (RTK) (IC50s of 1.5 nM, 2 nM, 2 nM, 5 nM, 6 nM, 6 nM, 8 nM, 0.5 nM, 29 nM, 5 nM, and 9 nM for Axl, MER, VEGFR3, VEGFR2, VEGFR1, KIT, FLT3, DDR2, DDR1, TRKA, TRKB, respectively.) , shows potent single-agent antitumor efficacy and enhances the activity of PD-1 blockade through promoting an antitumor immune microenvironment.
价 格：￥电议型 号：T12925产 地：中国大陆
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T12924Sitaxsentan；司他生坦TBC-11251|||IPI 1040；TBC-11251|||IPI 1040
Sitaxsentan (TBC-11251) is A selective endothelin A (ETA) receptor antagonist. Endothelin is an effective vasoconstrictor. Sitaxsentan blocks the binding of endothelin to its receptors, thereby eliminating the harmful effects of endothelin.
价 格：￥电议型 号：T12924产 地：中国大陆
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T1291Cisapride；西沙比利Prepulsid|||R 51619|||Pridesia|||Kaudalit|||(±)-Cisaprid|||Kinestase；西沙必利|||西沙比利|||Pre
Cisapride (R 51619) is a serotonin type 4 (5-HT4) receptor agonists are potent prokinetic agents that act on serotonin receptors in the intestine and promote intestinal peristalsis, increase gastric emptying and decrease esophageal reflux.
价 格：￥电议型 号：T1291产 地：中国大陆
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T12862SC58451；化合物SC58451SC58451
SC58451 is a novel potent, orally active and selective COX-2 inhibitor.SC58451 showed anti-inflammatory activity in a rat model of arthritis.
价 格：￥电议型 号：T12862产 地：中国大陆
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T12851SB290157 trifluoroacetate；化合物SB290157 trifluoroacetateSB290157 trifluoroacetate
SB290157 trifluoroacetate is a potent and selective antagonist of C3a receptor(IC50 of 200 nM).
价 格：￥电议型 号：T12851产 地：中国大陆
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T12848SB-657510；化合物SB-657510SB-657510
SB-657510 is a urotensin II (UII) receptor (UT) antagonist. The Ki values of UT for human, monkey, cat, rat and mouse were 61, 17, 30, 65 and 56 nM, respectively. SB-657510 plays an anti-inflammatory role by inhibiting UII-induced inflammatory mediators, such as adhesion molecules, in human vascular endothelial cells and upregulation of cytokines and tissue factors. SB 657510 has a therapeutic effect on diabetes-related atherosclerotic disease in diabetic mouse models.
价 格：￥电议型 号：T12848产 地：中国大陆
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T12823S516；化合物 T12823S516
S516 is an active CKD-516 metabolite and is a potent inhibitor of tubulin polymerization(IC50 of 4.29 μM), has marked antitumor activity.
价 格：￥电议型 号：T12823产 地：中国大陆
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T1280Nepafenac；奈帕芬胺AL 6515|||AHR 9434；AL 6515|||AHR 9434|||奈帕芬胺
Nepafenac (AHR 9434) is a Nonsteroidal Anti-inflammatory Drug. The mechanism of action of nepafenac is as a Cyclooxygenase Inhibitor. The chemical classification of nepafenac is Nonsteroidal Anti-inflammatory Compounds.
价 格：￥电议型 号：T1280产 地：中国大陆
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T12792S-8510 phosphate；化合物 T12792SB-737552 phosphate；SB-737552 phosphate
S-8510 phosphate is an agonist of inverse Benzodiazepine (BDZ) receptor(Kis of 34.6 nM, 36.2 nM for –GABA and +GABA respectively).
价 格：￥电议型 号：T12792产 地：中国大陆
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T12782RWJ-445167；化合物 T127823DP-10017；3DP-10017
RWJ-445167 is a thrombin and factor Xa dual inhibitor(Ki of 4.0 nM and 230 nM, respectively), with potent antithrombotic activity.
价 格：￥电议型 号：T12782产 地：中国大陆
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T12779Ru-32514；化合物 Ru-32514Ru-32514
Ru-32514 is a benzodiazepine receptor agonist that partially reverses stress-induced arousal in mice and is used in the study of neurological disorders.
价 格：￥电议型 号：T12779产 地：中国大陆
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T12778LRTI-13951-33；化合物 T12778LRTI-13951-33
RTI-13951-33 is an effective and brain-penetrant GPR88 agonist (EC50: 25 nM, in GPR88 cAMP functional assay).
价 格：￥电议型 号：T12778L产 地：中国大陆
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T12778RTI-13951-33 hydrochloride；化合物 T12778RTI-13951-33 hydrochloride (2244884-08-8 free base)；RTI-13951-3
RTI-13951-33 hydrochloride is a potent, selective, and brain-penetrant GPR88 agonist. RTI-13951-33 hydrochloride exhibited an EC 50 of 25 nM in vitro cAMP functional assay. RTI-13951-33 hydrochloride significantly reduces alcohol reinforcement and intake behaviors in rats [1].
价 格：￥电议型 号：T12778产 地：中国大陆
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T12751RORγt agonist 1；化合物 T12751RORgammat agonist 1|||RORγt agonist 1|||RORγt agonist 1|||RORrt agonist 1；
RORγt agonist 1 is a potent, orally bioavailable agonist of RORγt(EC50 of 20.8 nM).
价 格：￥电议型 号：T12751产 地：中国大陆
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T12682Emzadirib；化合物EmzadiribCYT-0851|||RAD51-IN-2；CYT-0851|||RAD51-IN-2
Emzadirib (RAD51-IN-2) is a potent RAD51 inhibitor with potential anticancer activity for the study of DNA damage repair.
价 格：￥电议型 号：T12682产 地：中国大陆
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T126551Kakisaponin A；化合物 Kakisaponin AKakisaponin A
Kakisaponin A is a useful organic compound for research related to life sciences. The catalog number is T126551 and the CAS number is 1003864-78-5.
价 格：￥电议型 号：T126551产 地：中国大陆
