T13436(E)-[6]-Dehydroparadol

(E)-[6]-Dehydroparadol, an oxidative metabolite of [6]-Shogaol, is a potent Nrf2 activator.

价 格：￥电议型 号：T13436产 地：中国大陆

PDK0248Compound PDK0248Compound PDK0248

价 格：￥电议型 号：PDK0248产 地：中国大陆

TN1042Chebulic acidInhibitor,Chebulic acid,inhibit

Chebulic acid, a phenolcarboxylic acid compound isolated from Terminalia chebula, has potent anti-oxidant activity,which breaks the cross-links of proteins induced by advanced glycation end-products (AGEs) and inhibits the formation of AGEs.It has effects against the progression of AGE-induced endothelial cell dysfunction,may constitute a promising intervention agent against diabetic vascular complications

价 格：￥电议型 号：TN1042产 地：中国大陆

T8392L(+)-Asparagine monohydrateL-Asparagine,amino,non-essential,Inhibitor,L(+) Asparagine monohydrate,ti

L(+)-Asparagine monohydrate is a non-essential amino acid, participate in neurological and metabolic regulation of tissue cell function.

价 格：￥电议型 号：T8392产 地：中国大陆

TP1122LIGF-I 30-41 acetate(82177-09-1 free base)IGF I 30 41 acetate(82177 09 1 free base),IGFI 3041 acetate

IGF-I 30-41 acetate is amino acids 30 to 41 fragment of Insulin-like Growth Factor I (IGF-I).

价 格：￥电议型 号：TP1122L产 地：中国大陆

T9330MIPS521A1AR,inhibit,MIPS-521,pain,Adenosine Receptor,MIPS 521,MIPS521,Inhibitor,P1 receptor

MIPS-521 is a positive allosteric modulator of the A1R.

价 格：￥电议型 号：T9330产 地：中国大陆

T8449TC-I2000TCI2000,TC-I-2000,TC I2000

TC-I2000 is an TRPM8 channel blocker. Inhibits icilin-induced TRPM8 channel activation in rTRPM8-expressing CHO cells with IC50 of 53 nM.

价 格：￥电议型 号：T8449产 地：中国大陆

T9627PHD-1-IN-1pocket,ion,Arg367-out,HIF-PH,Hypoxia-inducible factors,site,active,PHD 1 IN 1,orally,Inhib

PHD-1-IN-1 is a potent inhibitor of hypoxia-inducible factor prolylhydroxylase domain-1 (PHD-1) enzyme(IC50 = 0.034 μM).

价 格：￥电议型 号：T9627产 地：中国大陆

T10927Cyt-PTPε Inhibitor-1

Cyt-PTPε Inhibitor-1 is an inhibitor of cytosolic protein tyrosine phosphatase ε. Cyt-PTPε Inhibitor-1 blocks the dephosphorylation of c-Src and exhibits anti-osteoclastic activity.

价 格：￥电议型 号：T10927产 地：中国大陆

T13133Tetrabenazine MetaboliteTetrabenazine Metabolite

Tetrabenazine Metabolite is an active Tetrabenazine metabolite. Tetrabenazine Metabolite is a inhibitor of vesicular monoamine transporter 2 (VMAT2) (Ki=13.4 nM).

价 格：￥电议型 号：T13133产 地：中国大陆

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

T8394D-Serineinhibit,D-Serine,Ionotropic glutamate receptors,Endogenous Metabolite,Inhibitor,DSerine,iGlu

(R)-Serine is an endogenous amino acid,is a potent co-agonist at the NMDA glutamate receptor.

价 格：￥电议型 号：T8394产 地：中国大陆

T86424-CMTBshort-chain,4 CMTB,fatty,acids,ECL2,FFAR,Free Fatty Acid Receptor,4CMTB,GPCRs,4-CMTB,ago-allos

4-CMTB is a selective agonist of FFA2 and GPR43.It also is a positive allosteric modulator (pEC50=6.38).

价 格：￥电议型 号：T8642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

TL0006Cichoric Acidp-Akt,inhibit,ROS,anti-inflammatory,Apoptosis,glucose uptake,insulin resistance,glucosa

Chicoric Acid is a potent inhibitor of human immunodeficiency virus type-1 (HIV-1) integrase and the replication in tissues. It also a class of cannabinomimetics with CB2 receptor-dependent and independent.

价 格：￥电议型 号：TL0006产 地：中国大陆