CAS 951120-33-5

Formula: C14H8ClF2N3O2S

InChI: InChI=1S/C14H8ClF2N3O2S/c15-6-3-8-14(19-4-6)23-10(20-8)5-22-9-2-1-7(16)11(12(9)17)13(18)21/h1-4H,5H2,(H2,18,21)

InChI key: INYJNSBDHOVLAH-UHFFFAOYSA-N

SMILES: C1=CC(=C(C(=C1OCC2=NC3=C(S2)N=CC(=C3)Cl)F)C(=O)N)F

PC190723

CAS: 951120-33-5

PC190723

Formula: C₁₄H₈ClF₂N₃O₂S

Purezza: 97.5%

Peso molecolare: 355.75

Ref: 54-BUP01255

3-((6-Chlorothiazolo[5,4-b]pyridin-2-yl)methoxy)-2,6-difluorobenzamide

CAS: 951120-33-5

Formula: C₁₄H₈ClF₂N₃O₂S

Purezza: 97.64%

Colore e forma: Solid

Peso molecolare: 355.7470

Ref: IN-DA01DPIX

3-((6-Chlorothiazolo[5,4-b]pyridin-2-yl)methoxy)-2,6-difluorobenzamide

CAS: 951120-33-5

3-((6-Chlorothiazolo[5,4-b]pyridin-2-yl)methoxy)-2,6-difluorobenzamide

Formula: C₁₄H₈ClF₂N₃O₂S

Purezza: 98%

Peso molecolare: 355.75

Ref: IN-DG248418

3-[(6-Chlorothiazolo[5,4-b]pyridin-2-yl)methoxy]-2,6-difluorobenzamide

Prodotto controllato

CAS: 951120-33-5

Formula: C₁₄H₈ClF₂N₃O₂S

Colore e forma: Neat

Peso molecolare: 355.747

Ref: TR-C380180

PC 190723

CAS: 951120-33-5

PC 190723 is a synthetic chemical compound, which is derived through targeted chemical synthesis processes involving precise organic reactions. Its mode of action involves disrupting cellular division by inhibiting specific protein functions essential for the mitotic process. This molecular interaction results in potent effects on cell division, making it a valuable tool for studying cellular mechanics and developing therapeutic strategies.

Formula: C₁₄H₈ClF₂N₃O₂S

Purezza: Min. 95%

Peso molecolare: 355.75 g/mol

Ref: 3D-FC99088

PC190723

CAS: 951120-33-5

PC190723 is an inhibitor of the bacterial cytosolic protein FtsZ with antimicrobial activity against Staphylococcus spp.

Formula: C₁₄H₈ClF₂N₃O₂S

Purezza: 97.64%

Colore e forma: Yellow Solid

Peso molecolare: 355.75

Ref: TM-T61274