TN1438beta-Amyrin acetateHMG-CoA,betaAmyrin acetate,LDL,Fungal,inhibit,Inhibitor,arthritic,hemolysis,antif

beta-Amyrin acetate inhibits HMG-CoA Reductase (HMGCR) and sEH activity with IC50 of 3.4 μM. beta-Amyrin acetate has anti-inflammatory, antifungal, antioxidant, and anti-hyperlipidemic activities.

价 格：￥电议型 号：TN1438产 地：中国大陆

TP1722LPACAP (6-38), human, ovine, rat acetatePACAP (6 38), human, ovine, rat acetate(143748 18 9 Free base

PACAP (6-38), human, ovine, rat acetate is a potent PACAP receptor antagonist with IC50s of 30, 600, and 40 nM for PACAP type I receptor, PACAP type II receptor VIP1, and PACAP type II receptor VIP2, respectively.

价 格：￥电议型 号：TP1722L产 地：中国大陆

T9226CCG-143140CCG143140,CCG 143140

CCG-143140 is a GLP-1 receptor inverse agonists.

价 格：￥电议型 号：T9226产 地：中国大陆

T14362LAY 9944 dihydrochloride1(2chlorophenyl)N[[4[(2chlorophenyl)methylaminomethyl]cyclohexyl]methyl]metha

AY 9944 dihydrochloride is a intermediate.

价 格：￥电议型 号：T14362L产 地：中国大陆

T8143Bevantolol hydrochlorideBevantolol hydrochloride,Beta Receptor,Ca2+ channels,cerebral,Inhibitor,inhi

Bevantolol hydrochloride is a β1-adrenoceptor antagonist that treatment angina pectoris and hypertension.

价 格：￥电议型 号：T8143产 地：中国大陆

T23889CID-663143CID 663143

CID-663143 inhibits cancer cell growth and shows microtubule-binding activity.

价 格：￥电议型 号：T23889产 地：中国大陆

T6S1435Notopterolanti-inflammatory,antipyretic,Apoptosis,analgesic,Inhibitor,Coumarin,Notopterol,myeloid,le

1. Notopterol induces apoptosis and inhibits cell cycle-specific.

价 格：￥电议型 号：T6S1435产 地：中国大陆

Fr14395Compound Fr14395Compound Fr14395

价 格：￥电议型 号：Fr14395产 地：中国大陆

TP1434LLecirelin acetate(61012-19-9 free base)Lecirelin acetate(61012199 free base),Lecirelin acetate(61012

Lecirelin acetate is a synthetic GnRH (gonadotropin releasing hormone) analogue which shows a great efficacy in the treatment of bovine ovarian follicular cysts.

价 格：￥电议型 号：TP1434L产 地：中国大陆

T8409SYN1143c-Met/HGFR,SYN-1143,tumor,RON,dual,inhibit,SYN1143,SYN 1143,cancer,Inhibitor,c-Met

AMG-1 is a potent inhibitor of human RON and c-Met.In vitro kinase assays showed that compound I is a potent inhibitor of human RON and c-Met with IC50s of 9 and 4 nmol/L, respectively.

价 格：￥电议型 号：T8409产 地：中国大陆

T7336ICA-121431Nav,Na channels,inhibitor,ICA-121431,ICA 121431,TTX-resistant,Sodium Channel,channel,Na+ c

ICA-121431 is a nanomolar potent small molecule Nav1.7 channel inhibitor with IC50 of 19 nM for rat Nav1.7, with little or no activity against human Nav1.5 or Nav1.7 channels.

价 格：￥电议型 号：T7336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

TN71431,3-Diphenethylurea

1,3-Diphenethylurea is a marine derived natural products found in Lissoclinum patella.

价 格：￥电议型 号：TN7143产 地：中国大陆

TN1439Oleanolic acid 28-O-β-D-glucopyranosideOleanolic acid 28 O β D glucopyranoside,Inhibitor,inhibit,Ole

Beta-D-glucopyranosyl oleanolate is a natural product from Hedera nepalensis.

价 格：￥电议型 号：TN1439产 地：中国大陆

TQ0042BAY-1436032Inhibitor,BAY1436032,Isocitrate Dehydrogenase (IDH),BAY-1436032,inhibit,BAY 1436032

BAY-1436032 is a novel, selective and orally available inhibitor of pan-mutant isocitrate dehydrogenase 1 (IDH1).

价 格：￥电议型 号：TQ0042产 地：中国大陆

T22783FGIN-1-43FGIN143,FGIN 1 43

FGIN-1-43 is a potent and specific ligand for the mitochondrial DBI receptor.

价 格：￥电议型 号：T22783产 地：中国大陆

T67844RBN-3143RBN3143

RBN-3143 is a potent and inhibitor of NAD+-competitive catalytic PARP14 (IC50= 4 nM). RBN-3143 inhibits ADP-ribosylation mediated by PARP14 and stabilizes PARP14 in cell lines. RBN-3143 exhibits research potential of lung inflammation.

价 格：￥电议型 号：T67844产 地：中国大陆

T6422Brimonidine TartrateUK-14304,UK14304,AGN190342,Brimonidine,Adrenergic Receptor,AGN-190342,AGN 190342

Brimonidine tartrate is a quinoxaline derivative and adrenergic α-2 receptor agonist (EC50: 0.45 nM) that is used to manage intraocular pressure associated with open-angle glaucoma or ocular hypertension.

价 格：￥电议型 号：T6422产 地：中国大陆

T14303Alrizomadlin

Alrizomadlin is an orally active inhibitor of MDM2 with IC50 of 3.8 nM and Ki of 1 nM, respectively[1]. Alrizomadlin blocks the interaction of MDM2 and p53 and induces cell-cycle arrest and apoptosis in a p53-dependent manner.

价 格：￥电议型 号：T14303产 地：中国大陆

T7424NDI-091143NDI 091143,ACLY,inhibit,ATP Citrate Lyase,NDI-091143,NDI091143,Inhibitor

NDI-091143 is a potent and high-affinity human ATP-citrate lyase (ACLY) inhibitor with an IC50 of 2.1 nM (ADP-Glo assay),indirectly disrupting citrate binding via an unexpected mechanism of inhibition.

价 格：￥电议型 号：T7424产 地：中国大陆