CAS 951120-33-5

Formule : 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)

Code InChI : 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

Formule : C₁₄H₈ClF₂N₃O₂S

Degré de pureté : ≥95%

Masse moléculaire : 355.75

Ref: 54-BUP01255

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

CAS : 951120-33-5

Degré de pureté : 97.64%

Ref: IN-DA01DPIX

PC190723

CAS : 951120-33-5

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

Formule : C₁₄H₈ClF₂N₃O₂S

Degré de pureté : 98%

Masse moléculaire : 355.75

Ref: IN-DG248418

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

Produit contrôlé

CAS : 951120-33-5

Formule : C₁₄H₈ClF₂N₃O₂S

Couleur et forme : Neat

Masse moléculaire : 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.

Formule : C₁₄H₈ClF₂N₃O₂S

Degré de pureté : Min. 95%

Masse moléculaire : 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.

Formule : C₁₄H₈ClF₂N₃O₂S

Degré de pureté : 97.64%

Couleur et forme : Yellow Solid

Masse moléculaire : 355.75

Ref: TM-T61274