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T131127Citroside A or B；化合物 Citroside A or BCitroside A or B
Citroside A or B is a useful organic compound for research related to life sciences and the catalog number is T131127.
价 格：￥电议型 号：T131127产 地：中国大陆
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T13017STL127705；化合物STL127705Compound L|||7-[[2-(3,4-Dimethoxyphenyl)ethyl]amino]-3-(3-fluorophenyl)pyrimid
STL127705 (Compound L) is a potent Ku 70/80 heterodimer protein inhibitor and inhibits Ku70/80-DNA interaction with IC50 of 3.5 μM. STL127705 inhibits the activation of Ku-dependent DNA-PKCS kinase with IC50 of 2.5 μM.
价 格：￥电议型 号：T13017产 地：中国大陆
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T1283Clinafloxacin；克林沙星PD 127391|||CI-960|||AM-1091；克林沙星|||PD 127391|||CI-960|||AM-1091
Clinafloxacin (CI-960)(PD-127391) is a fluoroquinolone antibiotic.
价 格：￥电议型 号：T1283产 地：中国大陆
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T12814(S)-Tenofovir；(S)-替诺福韦(S)-替诺福韦|||(S)-替诺福韦|||(S)-PMPA|||GS-1278|||TDF|||(S)-PMPA|||(S)-GS 1278|||(S)T
(S)-Tenofovir ((S)-PMPA) is the less active S-enantiomer of Tenofovir which is a nucleotide reverse transcriptase inhibitor.
价 格：￥电议型 号：T12814产 地：中国大陆
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T12799(S)-Hydroxychloroquine；化合物 T12799(S)-HCQ；(S)-HCQ
(S)-Hydroxychloroquine is the enantiomer of Hydroxychloroquine. Hydroxychloroquine shows efficiently inhibits SARS-CoV-2 infection in vitro.
价 格：￥电议型 号：T12799产 地：中国大陆
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T12798(S)-GNE-987；化合物 T12798(S)-GNE-987
(S)-GNE-987 binds to the BRD4 BD1(IC50=4 nM) and BD2 (3.9 nM) bromodomains and can be used to design PROTAC-Antibody Conjugate (PAC).
价 格：￥电议型 号：T12798产 地：中国大陆
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T12797LRU-SKI 43 hydrochloride；RU-SKI 43（盐酸盐）RU-SKI 43 hydrochloride
RU-SKI 43 hydrochloride is a potent and selective inhibitor of Hedgehog acyltransferase (Hhat)(IC50 of 850 nM), has anti-cancer activity.
价 格：￥电议型 号：T12797L产 地：中国大陆
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T12797RU-SKI 43；化合物RU-SKI 43RUSKI 43；RUSKI 43
RU-SKI 43 is a potent and selective hedgehog acyltransferase (Hhat) inhibitor with an IC50 of 850 nM.RU-SKI 43 has anticancer activity and is a potential compound for the treatment of lung adenocarcinomas.RU-SKI 43 reduces Gli-1 activation through smoothing-independent non-canonical signalling and inhibits Akt and mTOR pathway activity.
价 格：￥电议型 号：T12797产 地：中国大陆
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T12796S-Dihydrodaidzein；S-二氢大豆苷元(3S)-7-hydroxy-3-(4-hydroxyphenyl)-2,3-dihydrochromen-4-one；S-二氢大豆苷元|||(3S
S-Dihydrodaidzein ((3S)-7-hydroxy-3-(4-hydroxyphenyl)-2,3-dihydrochromen-4-one) is an enantiomer of dihydrodaidzein which is involved in equol biosynthesis in a lactic acid bacterium, Lactococcus sp. strain.
价 格：￥电议型 号：T12796产 地：中国大陆
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T12795(S)-Ceralasertib；化合物 T12795(S)-AZD6738；(S)-AZD6738
(S)-Ceralasertib is a potent and selective inhibitor of sulfoximine morpholinopyrimidine ATR with excellent preclinical physicochemical and pharmacokinetic (PK) characteristics. .
价 格：￥电议型 号：T12795产 地：中国大陆
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T12794(S)-Carvedilol；(S)-卡维地洛(S)-BM 14190；(S)-BM 14190|||(S)-卡维地洛
(S)-Carvedilol is a non-selective β/α-1 blocker.It exerts protection against the vascular or cardiac toxicity of Doxorubicin (DOX).
价 格：￥电议型 号：T12794产 地：中国大陆
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T12793(S)-BI 665915；化合物 T12793(S)-BI 665915
(S)-BI 665915 is an orally active inhibitor of oxadiazole-containing 5-lipoxygenase-activating protein (FLAP)(IC50 of 1.7 nM for FLAP binding)..
价 格：￥电议型 号：T12793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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T12791(S)-3-Hydroxy Midostaurin；化合物 T12791(S)-CGP52421；(S)-CGP52421
(S)-3-Hydroxy Midostaurin is a potent inhibitor of kinases(IC50 of <400 nM for 13 kinases (VEGFR-2, TRK-A, FLT3, et)).
价 格：￥电议型 号：T12791产 地：中国大陆
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T12790Guadecitabine sodium；化合物 T12790SGI-110 sodium|||S-110 sodium；SGI-110 sodium|||S-110 sodium
Guadecitabine sodium is a inhibitor of second-generation DNA methyltransferases (DNMT) .
价 格：￥电议型 号：T12790产 地：中国大陆
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T1279Vilazodone；维拉佐酮SB659746A|||EMD 68843；维拉佐酮|||SB659746A|||EMD 68843
Vilazodone (SB659746A) is a selective serotonin (5-HT) reuptake inhibitor (SSRI) and a 5-HT-1A receptor partial agonist, with antidepressant and anti-anxiety activities. Vilazodone inhibits the reuptake of serotonin from the synaptic cleft while stimulating the release of 5-HT into the synaptic cleft. This increases the concentration of 5-HT in the synaptic cleft and potentiates serotonergic neurotransmission in the central nervous system.
价 格：￥电议型 号：T1279产 地：中国大陆
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T12789S-1-Propenyl-L-cysteine；化合物 T12789S-1-Propenyl-L-cysteine
S-1-Propenyl-L-cysteine, a stereoisomer of S-allyl-l-cysteine, exhibits immunomodulatory effects and has been shown to decrease blood pressure in hypertensive animal models.
价 格：￥电议型 号：T12789产 地：中国大陆
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T12788R(+)-IAA-94；化合物R(+)-IAA-94R(+)-Methylindazone；R(+)-Methylindazone
R(+)-IAA-94 (R(+)-Methylindazone) is a potent indanyloxyacetic acid blocker of epithelial chloride channels. R(+)-IAA-94 inhibits Nef-sdAb19 (single-domain antibody) interaction and binds to negative factor (Nef).
价 格：￥电议型 号：T12788产 地：中国大陆
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T12787Ryanodine；化合物 T12787Ryanodine
Ryanodine, a diterpenoid poison derived from Ryania speciosa, acts as a modulator of the ryanodine receptor, which is permeable to cells. Depending on its concentration, ryanodine can either stimulate or inhibit Ca2+ release mediated by these receptors.
价 格：￥电议型 号：T12787产 地：中国大陆
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T12786RY785；化合物RY785RY785
RY785 is a potent and selective inhibitor of voltage-gated potassium channel such as KV2.2 (IC50 = 50 nM). RY785 may be used in pain relief studies.
价 格：￥电议型 号：T12786产 地：中国大陆
