
CAS 222716-34-9
:Formula:C24H24N2O3S
InChI:InChI=1S/C24H24N2O3S/c1-2-15-12-16-22(28)18(24-25-19-8-4-5-9-20(19)30-24)14-29-23(16)17(21(15)27)13-26-10-6-3-7-11-26/h4-5,8-9,12,14,27H,2-3,6-7,10-11,13H2,1H3
InChI key:JKIXLEKBXHMXTN-UHFFFAOYSA-N
SMILES:CCC1=CC2=C(C(=C1O)CN3CCCCC3)OC=C(C2=O)C4=NC5=CC=CC=C5S4
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3-(Benzo[D]Thiazol-2-Yl)-6-Ethyl-7-Hydroxy-8-(Piperidin-1-Ylmethyl)-4H-Chromen-4-One
CAS:Formula:C24H24N2O3SPurezza:99%Colore e forma:SolidPeso molecolare:420.52403-(Benzo[D]Thiazol-2-Yl)-6-Ethyl-7-Hydroxy-8-(Piperidin-1-Ylmethyl)-4H-Chromen-4-One
CAS:3-(Benzo[D]Thiazol-2-Yl)-6-Ethyl-7-Hydroxy-8-(Piperidin-1-Ylmethyl)-4H-Chromen-4-OneFormula:C24H24N2O3SPurezza:99%Peso molecolare:420.52SZL P1-41
CAS:SZL P1-41 inhibits Skp2, blocks complex formation, and halts ubiquitination, promoting cell senescence, reducing glycolysis, and exhibiting antitumor effects.Formula:C24H24N2O3SPurezza:99.60% - 99.87%Colore e forma:SolidPeso molecolare:420.524SZL P1-41
CAS:3-(Benzo[d]thiazol-2-yl)-6-ethyl-7-hydroxy-8-(piperidin-1-ylmethyl)-4H-chromen-4-oneFormula:C24H24N2O3SPurezza:99%Peso molecolare:420.523-(BENZO[D]THIAZOL-2-YL)-6-ETHYL-7-HYDROXY-8-(PIPERIDIN-1-YLMETHYL)-4H-CHROMEN-4-ONE
CAS:Purezza:99%Peso molecolare:420.5299988Ref: 10-F826886
10mgPrezzo su richiesta50mgPrezzo su richiesta100mgPrezzo su richiesta250mgPrezzo su richiesta5mg90,00€3-(2-Benzothiazolyl)-6-ethyl-7-hydroxy-8-(1-piperidinylmethyl)-4H-1-benzopyran-4-one
CAS:Prodotto controllatoStability Hygroscopic
Applications 3-(2-Benzothiazolyl)-6-ethyl-7-hydroxy-8-(1-piperidinylmethyl)-4H-1-benzopyran-4-one is involved in the pharmacological inactivation of Skp2 E3 ligase.
References Chan, C., et al.: Cell, 154, 556-568 (2013)Formula:C24H24N2O3SColore e forma:NeatPeso molecolare:420.52SZL P1-41
CAS:SZL P1-41 is a secretase inhibitor that inhibits the activity of ubiquitin ligases. It has been shown to inhibit the progress of Alzheimer's disease in wild-type mice, and it also inhibits cell growth and proliferation in prostate cancer cells. SZL P1-41 inhibits the fibrillization of amyloid protein by preventing its binding to other proteins, which decreases the production of beta-amyloid peptides. This drug is currently being investigated as a potential anticancer agent due to its ability to inhibit cell cycle progression and induce apoptosis.Formula:C24H24N2O3SPurezza:Min. 95%Peso molecolare:420.52 g/mol






