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

TP1240Adrenocorticotropic Hormone (ACTH) (18-39), human TFAinhibit,Adrenocorticotropic Hormone (ACTH) (18-

Adrenocorticotropic Hormone (ACTH) (18-39), human TFA is a corticotropinlike intermediate lobe peptide, it is is produced in the melanotrophs of the intermediate lobe of the pituitary.

价 格：￥电议型 号：TP1240产 地：中国大陆

T40146Sec61-IN-1Sec61IN1,Sec61 IN 1,Sec-61-IN-1

Sec61-IN-1 is a potent sec61 inhibitor (Patent WO2020176863A1, compound A317).

价 格：￥电议型 号：T40146产 地：中国大陆

T3899Calceolarioside BInhibitor,inhibit,Calceolarioside B

Calceolarioside B displays inhibition of aromatase. Calceolarioside B displays inhibition of human recombinant PKCalpha.

价 格：￥电议型 号：T3899产 地：中国大陆

TQ0083NI-57Inhibitor,inhibit,NI 57,NI-57,NI57,Epigenetic Reader Domain

NI-57 is an inhibitor of proteins of bromodomain and plant homeodomain finger-containing (BRPF) family, with IC50s of 3.1, 46 and 140 nM for BRPF1, BRPF2 (BRD1) and BRPF3, respectively.

价 格：￥电议型 号：TQ0083产 地：中国大陆

Fr212652-Methyl-2H-indazole-3-carboxylic acid

价 格：￥电议型 号：Fr21265产 地：中国大陆

PDK0225Compound PDK0225Compound PDK0225

价 格：￥电议型 号：PDK0225产 地：中国大陆

TN2347Methylsticinkava,Methylsticin,Inhibitor,inhibit,osteoclast

Methysticin is a kavalactone isolated from the kava roots. Methylsticin exhibit osteoclast formation inhibitory activity. It inhibits activation of NF-χB in lung adenocarcinoma tissue, activates Nrf2 in neurons and astroglia, decreases peak amplitude of voltage-gated Na+ channels in hippocampal neurons, and suppresses growth of Fusarium, Trichoderma, and Colletotrichum.

价 格：￥电议型 号：TN2347产 地：中国大陆

TN6444Cyclo(Tyr-Leu)Inhibitor,Cyclo(TyrLeu),Cyclo(Tyr-Leu),Cyclo(Tyr Leu),inhibit

Cyclo(Tyr-Leu) is a cyclic dipeptide from Portulaca oleracea Linn with cytotoxicity, antifungal, and anticoagulant activities.

价 格：￥电议型 号：TN6444产 地：中国大陆

TN1029Hosenkoside Cinhibit,Inhibitor,Hosenkoside C

Hosenkoside C is a baccharane glycoside found in the seeds of Impatiens balsamina.

价 格：￥电议型 号：TN1029产 地：中国大陆

TQ0267Endomorphin 1Endomorphin 1,inhibit,Endomorphin1,Opioid Receptor,Inhibitor

Endomorphin 1 is a high affinity and selective agonist of the μ-opioid receptor and displays reasonable affinities for kappa3 binding sites (Ki: 20~30 nM).

价 格：￥电议型 号：TQ0267产 地：中国大陆

TP1417LSakamototide substrate peptide acetateSakamototide substrate peptide acetate

Sakamototide substrate peptide acetate is a peptide substrate of AMPK kinase family and can be used for the determination of kinase activity.

价 格：￥电议型 号：TP1417L产 地：中国大陆

T32873Maralixibat Chloride

Maralixibat Chloride, an apical, sodium-dependent, bile acid transport inhibitor, prevents enterohepatic bile acid recirculation.

价 格：￥电议型 号：T32873产 地：中国大陆

TN6972Methyl pentadecanoateInhibitor,inhibit,Methyl pentadecanoate

Methyl pentadecanoate is a natural product.Methyl pentadecanoate is a saturated fatty acid methyl ester obtained from the esterification of myristic acid. Methyl myristate shows a high melanin induction in B16F10 melanoma[1].

价 格：￥电议型 号：TN6972产 地：中国大陆

T6566Levobupivacaine hydrochlorideCNS toxicity,gastric cancer,Na channels,Erastin,Inhibitor,analgesic,ana

Levobupivacaine HCl is a reversible neuronal sodium channel inhibitor, which is the pure S(-)-enantiomer of bupivacaine. It was utilized as a long-acting local anesthetic.

价 格：￥电议型 号：T6566产 地：中国大陆

T8678NaphthazarinNaturally,Apoptosis,Naphthazarin,stress,microtubules,mitochondrial,AIF,Inhibitor,p21,lys

Naphthazarin is effective by various cellular mechanisms including oxidative stress, activation of mitochondrial apoptosis-inducing factor (AIF), depolymerization of microtubules, interference with lysosomal function and p53-dependent p21 activation. It triggers apoptosis and has anti-tumor effects

价 格：￥电议型 号：T8678产 地：中国大陆

T7013VorapaxarProtease Activated Receptor (PAR),Inhibitor,SCH-530348,Vorapaxar,SCH530348,Thrombin recepto

Vorapaxar (SCH 530348) is an effective and orally active thrombin receptor (PAR-1) antagonist (Ki: 8.1 nM).

价 格：￥电议型 号：T7013产 地：中国大陆

T7265HSP27 inhibitor J2Heat shock proteins,inhibit,HSP-27 inhibitor J2,HSP27 inhibitor J2,Inhibitor,J 2,H

HSP27 inhibitor J2 (J2) is a HSP27 inhibitor, inhibits a production of HSP27 giant polymers, thereby having an effect of inhibiting a chaperone function of the HSP27 and reducing a cell protection function.

价 格：￥电议型 号：T7265产 地：中国大陆

T131725Compound TCFN92660

价 格：￥电议型 号：T131725产 地：中国大陆