CAS 1807758-81-1

Formula: C15H12ClN3O

InChI: InChI=1S/C15H12ClN3O/c16-11-6-4-10(5-7-11)14-9-18-15(20-14)19-13-3-1-2-12(17)8-13/h1-9H,17H2,(H,18,19)

InChI key: RMRVZWMKRCLSFX-UHFFFAOYSA-N

SMILES: C1=CC(=CC(=C1)NC2=NC=C(O2)C3=CC=C(C=C3)Cl)N

SIRT7 inhibitor 97491

CAS: 1807758-81-1

SIRT7 inhibitor 97491

Formula: C₁₅H₁₂ClN₃O

Purezza: ≥98%

Peso molecolare: 285.73

Ref: 54-BUP02940

N1-(5-(4-Chlorophenyl)oxazol-2-yl)benzene-1,3-diamine

CAS: 1807758-81-1

Formula: C₁₅H₁₂ClN₃O

Purezza: 97%

Colore e forma: Solid

Peso molecolare: 285.7283

Ref: IN-DA01V51B

SIRT7 inhibitor 97491

CAS: 1807758-81-1

N1-(5-(4-Chlorophenyl)oxazol-2-yl)benzene-1,3-diamine

Formula: C₁₅H₁₂ClN₃O

Purezza: 97%

Peso molecolare: 285.73

Ref: IN-DG01168133

SIRT7 inhibitor 97491

CAS: 1807758-81-1

SIRT7 inhibitor 97491 is an HDAC inhibitor with high specificity for SIRT7 (IC50 = 325 nM). SIRT7 inhibitor 97491 promotes apoptosis through caspase pathway.

Formula: C₁₅H₁₂ClN₃O

Purezza: 99.75%

Colore e forma: Solid

Peso molecolare: 285.728

Ref: TM-T39233

Sirt7 inhibitor 97491

CAS: 1807758-81-1

Sirt7 inhibitor 97491 is an anticancer drug that works by inhibiting the activity of Sirt7, a protein that promotes tumor growth. This inhibitor has been shown to be effective in human cancer cell lines and may have potential for use in cancer therapy. The drug has been tested in Chinese hamster ovary cells and was found to induce apoptosis, or programmed cell death, in these cells. Sirt7 inhibitor 97491 is an analog of chloroquine and can also inhibit kinases, which are enzymes involved in signaling pathways that regulate cell growth and division. In addition, this inhibitor has been found to increase the effectiveness of other anticancer drugs such as artesunate. Overall, Sirt7 inhibitor 97491 is a promising new drug candidate for the treatment of cancer.

Formula: C₁₅H₁₂ClN₃O

Purezza: Min. 95%

Colore e forma: Powder

Peso molecolare: 285.73 g/mol

Ref: 3D-HXC75881