TP1485LCalcineurin substrate acetateCalcineurin substrate acetate

Calcineurin substrate acetate is from the regulatory RII subunit of cAMP-dependent protein kinase.

价 格：￥电议型 号：TP1485L产 地：中国大陆

TP1741LHistatin 5 acetateHistatin 5 acetate

Histatin 5 acetate inhibits the activity of the host matrix metalloproteinases MMP-2 and MMP-9 with IC50s of 0.57 and 0.25 μM, respectively.

价 格：￥电议型 号：TP1741L产 地：中国大陆

T99683-Piperidinyl(1-pyrrolidinyl)methanone hydrochloride3Piperidinyl(1pyrrolidinyl)methanone hydrochlori

3-Piperidinyl(1-pyrrolidinyl)methanone hydrochloride can be used in the synthesis of piperidin-4-yl-urea derivatives which are MCH-R1 antagonists.

价 格：￥电议型 号：T9968产 地：中国大陆

T6425BTZ043 RacemateBenzothiazinone10526038,inhibit,Benzothiazinone-10526038,BTZ043 Racemate,BTZ 10526038

BTZ043 racemate is a decaprenylphosphoryl-β-D-ribose 2´-epimerase (DprE1) inhibitor, used as a new antimycobacterial agent.

价 格：￥电议型 号：T6425产 地：中国大陆

T8988PythiDCPythiDC

PythiDC is a selective collagen prolyl 4-hydroxylase inhibitor, neither causing general toxicity nor disrupting iron homeostasis.

价 格：￥电议型 号：T8988产 地：中国大陆

TN7058DihydrolapachenoleInhibitor,Dihydrolapachenole,inhibit

dihydrolapachenol is a natural isolated from the heartwood of T. chrysantha.

价 格：￥电议型 号：TN7058产 地：中国大陆

T9678ML328ML328,ML-328

ML328 is a potent and selective inhibitor of bacterial AddAB(IC50 = 1.0 μM) and RecBCD(IC50 = 4.8 μM) helicase-nucleases.

价 格：￥电议型 号：T9678产 地：中国大陆

T7093RafoxanideHemonchus,Rafoxanide,energy metabolism,inhibit,antiparasitic,Parasite,Fasciola,Estrus ovis

Rafoxanide as a dual CDK4/6 inhibitor for the treatment of skin cancer. Rafoxanide is a salicylanilide used as an anthelmintic. It is used to treat fluke, hookworm and other infestations.

价 格：￥电议型 号：T7093产 地：中国大陆

T11358gamma-secretase modulator 1

gamma-secretase modulator 1 is a modulator of γ secretase and can be used in studies about the treatment of Alzheimer´s disease.

价 格：￥电议型 号：T11358产 地：中国大陆

T94371-methoxycyclopropanecarboxylic acid1methoxycyclopropanecarboxylic acid,1 methoxycyclopropanecarboxy

1-methoxycyclopropanecarboxylic acid is an agonist of free fatty acid receptor 3 (FFAR3, human).

价 格：￥电议型 号：T9437产 地：中国大陆

T1782LCanagliflozin hemihydrate

Canagliflozin hemihydrate is a drug of the gliflozin class or subtype 2 sodium-glucose transport inhibitors used for the treatment of type 2 diabetes. SGLT2 is responsible for at least 90% of renal glucose reabsorption (SGLT1 being responsible for the remaining 10%). Blocking this transporter causes up to 119 grams of blood glucose per day to be eliminated through the urine, corresponding to 476 kilocalories.

价 格：￥电议型 号：T1782L产 地：中国大陆

T6940PHA-767491 hydrochloridePHA767491,PHA 767491,inhibit,CAY-10572,Cyclin dependent kinase,CDK,CAY 10572

PHA-767491 is an effective ATP-competitive dual Cdc7/CDK9 inhibitor (IC50: 10/34 nM). It has ~20-fold selectivity against GSK3-β and CDK1/2, 50-fold selectivity against CDK5 and MK2, 100-fold selectivity against CHK2 and PLK1.

价 格：￥电议型 号：T6940产 地：中国大陆

T8419XP-59XP 59,XP59,inhibit,Inhibitor,SARS-CoV,XP-59,SARS coronavirus

XP-59 is a potent the SARS-CoV Mpro inhibitor(Ki : 0.1 μM).

价 格：￥电议型 号：T8419产 地：中国大陆

T8478SC-43antiproliferative,Inhibitor,SC-43,SHP-1,PTPN6,Phosphatase,Apoptosis,caspase-3,SC 43,anti-fibrot

SC-43 is a potent and orally active agonist of SHP-1 (PTPN6). SC-43 inhibits the phosphorylation of STAT3 and induces cell apoptosis, and with anti-fibrotic and anticancer effects.

价 格：￥电议型 号：T8478产 地：中国大陆

T80582-Methyl-4-pentenoic Acidinhibit,Inhibitor,2 Methyl 4 pentenoic Acid,2Methyl4pentenoic Acid

2-Methyl-4-pentenoic acid is a branched-chain fatty acid.

价 格：￥电议型 号：T8058产 地：中国大陆

T2573MisoprostolMisoprostol

价 格：￥电议型 号：T2573产 地：中国大陆

T6S0078Oxypeucedanin hydrateInhibitor,inhibit,Oxypeucedanin,(+)-Oxypeucedanin,Oxypeucedanin hydrate,D. anet

1. Oxypeucedanin hydrate has antioxidant activity. 2. Oxypeucedanin hydrate is an antimutagenic agent. 3. Oxypeucedanin hydrate exhibits carbohydrate metabolizing enzymes inhibitory effect.

价 格：￥电议型 号：T6S0078产 地：中国大陆

T6778BDA-366Inhibitor,BDA-366,Antitumor,Bcl-2 Family,inhibit,Bcl2-BH4 domain,Anticancer,BDA 366,Antiapopt

BDA-366 is a potent Bcl2 antagonist, binding Bcl2-BH4 domain with high affinity and selectivity (Ki = 3.3 nM). BDA-366 induces conformational change in Bcl2 that abrogates its antiapoptotic function, converting it from a survival molecule to a cell death inducer. BDA-366 suppresses growth of lung cancer cells[1].

价 格：￥电议型 号：T6778产 地：中国大陆

T22808GR 46611

GR 46611 is a selective 5-HT1B and 5-HT1D receptor agonist and can be used in studies about the treatment of epilepsy.

价 格：￥电议型 号：T22808产 地：中国大陆

TN1028MilitarineMilitarine,inhibit,Inhibitor

Militarine has plant inhibitory effect against the growth of Italian ryegrass, timothy, and B. striata.

价 格：￥电议型 号：TN1028产 地：中国大陆