T1016011β-HSD1-IN-111β-HSD-1-IN-1,11βHSD1IN1,11β HSD1 IN 1

11β-HSD1-IN-1 is an inhibitor of 11β-hydroxydehydrogenase 1 (11β-HSD1, IC50: 52 nM), and used for the treatment of pain.

价 格：￥电议型 号：T10160产 地：中国大陆

Fr14015Compound Fr14015Compound Fr14015

价 格：￥电议型 号：Fr14015产 地：中国大陆

T6435CCT129202inhibit,CCT-129202,CCT 129202,Inhibitor,CCT129202,Aurora Kinase

CCT129202 is an ATP-competitive pan-Aurora inhibitor for Aurora A, Aurora B and Aurora C with IC50 of 0.042 μM, 0.198 μM and 0.227 μM, respectively. It is less potent to FGFR3, GSK3β, PDGFRβ, etc.

价 格：￥电议型 号：T6435产 地：中国大陆

TP1913L1BA 1 acetate(183241-31-8 free base)BA 1 acetate(183241 31 8 free base),BA 1 acetate(183241318 free b

BA 1 acetate is a potent bombesin receptor agonist (IC50 values are 0.26, 1.55 and 2.52 nM for BB1, BB2 and BB3 respectively). Enhances glucose transport in obese and diabetic primary myocytes. Also stimulates NCI-H1299 lung cancer cell proliferation in vitro.

价 格：￥电议型 号：TP1913L1产 地：中国大陆

T7839Lasofoxifene Tartrateosteoporosis,inhibit,Estrogen Receptor/ERR,arthritis,CP 336156,endocrine resist

Lasofoxifene Tartrate is a third-generation, non-steroidal selective estrogen receptor modulator.

价 格：￥电议型 号：T7839产 地：中国大陆

T8517BelinostatHistone deacetylases,PX-105684,PX 105684,Inhibitor,HDAC,Belinostat,PXD 101,inhibit,Autopha

Belinostat is an inhibitor of hydroxamic acid-type histone deacetylase (HDAC, IC50 of 27 nM in HeLa cell extracts),and with antineoplastic activity.

价 格：￥电议型 号：T8517产 地：中国大陆

T60164UNC7467UNC7467

UNC7467 is a potent IP6K inhibitor with values of 4.9, 8.9 and 1320 nM for IP6K2, IP6K1 and IP6K6, respectively. UNC7467 reduces levels of inositol pyrophosphates without significantly perturbing levels of other inositol phosphates. UNC7467 can be used for obesity research [1].

价 格：￥电议型 号：T60164产 地：中国大陆

T22871IpsapironeIpsapirone

Ipsapirone is a partial agonist of 5-HT1A receptor and produces an inhibitory effect on 5-HT2 and the α1-adrenergic function at high doses.

价 格：￥电议型 号：T22871产 地：中国大陆

T25282CYM 50358 hydrochloride (1314212-39-9 free base)CYM 50358 hydrochloride (1314212 39 9 free base),CYM

CYM50358 HCl is an S1P4 antagonist.

价 格：￥电议型 号：T25282产 地：中国大陆

TP1433CMD178 TFACMD178 TFA,CMD-178 TFA

CMD178 (TFA) is a lead peptide that consistently reduces the expression of Foxp3 and STAT5 induced by IL-2/s IL-2Rα signaling.

价 格：￥电议型 号：TP1433产 地：中国大陆

T8976PD-089828EGFR,ATP,nonselective,PD 089828,PDGFR,autophosphorylation,PD089828,HER1,Epidermal growth fa

PD 089828 is a competitive inhibitor of the receptor tyrosine kinases FGFR1, PDGFRβ, and EGFR (IC50s = 0.15, 1.76, and 5.47 μM, respectively) and a noncompetitive inhibitor of the nonreceptor tyrosine kinase c-Src (IC50 = 0.18 μM)

价 格：￥电议型 号：T8976产 地：中国大陆

T13362XY101XY101,XY-101

XY101 is a selective, metabolically stable and orally available agonist of RORγ inverse(IC50 of 30 nM and a Kd of 380 nM).

价 格：￥电议型 号：T13362产 地：中国大陆

T8649TMBIM6 antagonist-1TMBIM-6 antagonist-1,TMBIM6 antagonist 1,HT1080,SKBR3,TMBIM6 antagonist1,MCF7,Mam

BIA is a bax inhibitor

价 格：￥电议型 号：T8649产 地：中国大陆

T9591YCN47284YCN47284,YCN-47284

YCN47284 is an antimalarial compound with an IC50 of 1 μM for P. falciparum.

价 格：￥电议型 号：T9591产 地：中国大陆

T60110KN1022KN1022

KN1022 is an inhibitor of phosphorylation of platelet-derived growth factor (PDGF) receptor with IC50 of 0.26 μM.

价 格：￥电议型 号：T60110产 地：中国大陆

T10063LDL-IN-3LDLIN3,LDL IN 3

LDL-IN-3 shows anti-atherosclerotic and antioxidant activities.

价 格：￥电议型 号：T10063产 地：中国大陆

T8532IM156IM-156,IM156

IM156 (HL156A; HL271 acetate) is a chemical derivative of Metformin. IM156 is a potent and orally active AMPK activator that increases AMPK phosphorylation. IM156 attenuates aging-associated cognitive impairment in animal model [1] [2]. IM156 is a potent oxidative phosphorylation (OXPHOS) inhibitor which is able to be used for the research of solid tumors [3].

价 格：￥电议型 号：T8532产 地：中国大陆

TP1015NFAT Inhibitorinhibit,NFAT Inhibitor 1,dephosphorylation,cell-permeable,NFAT-Luc,NFAT Inhibitor-1,In

NFAT inhibitor is a cell-permeable compound that selectively inhibits calcineurin-mediated dephosphorylation of NFAT.

价 格：￥电议型 号：TP1015产 地：中国大陆

TN1154NepetinInhibitor,Nepetin,inhibit

6-Methoxyluteolin has antioxidant activity, it is a potent inhibitor of histamine release and calcium influx via down-regulation of the FcεRI α chain.

价 格：￥电议型 号：TN1154产 地：中国大陆

TP2312MOTS-c(Human) Acetate（1627580-64-6 free）MOTSc(Human) Acetate（1627580646 free）,MOTS c(Human) Acetate（

MOTS-c(Human) Acetate is a mitochondrial-derived peptide. MOTS-c(human) acetate induces the accumulation of AMP analog AICAR, increases activation of AMPK and expression of its downstream GLUT4. MOTS-c(human) acetate induces glucose uptake and improves insulin sensitivity. MOTS-c(human) acetate has implications in the regulation of obesity, diabetes, exercise, and longevity.

价 格：￥电议型 号：TP2312产 地：中国大陆