Product Name :
Caspase-3/7 Inhibitor I
Description:
Caspase-3/7 inbibitor I is a potent, reversible, isatin sulfonamide-based inhibitor of caspase-3 (KI(app) = 60 nM) and caspase-7 (KI(app) = 170 nM). Is a weaker inhibitor of caspase-9 (Ki(app) = 3.1 mM). It Has only a trivial effect (Ki(app) >25 mM) on the activities of caspase-1, caspase-2, caspase-4, caspase-6, and caspase-8. It has been shown to inhibit apoptosis in camptothecin treated Jurkat cells (IC50 ~50 µM). Also it has been reported to inhibit apoptosis in chondrocytes (44% inhibition at 10 µM and 98% inhibition at 50 µM). Selectivity for caspases-3 and 7 involves unique hydrophobic residues in the S2 pocket surrounding the catalytic cysteine residue. In some systems inhibition of caspases-3 and -7 can prevent apoptosis and may therefore have important therapeutic implications. A potent, cell-permeable, and specific, reversible inhibitor of caspase-3 (Ki = 60 nM) and caspase-7 (Ki = 170 nM).
CAS:
220509-74-0
Molecular Weight:
324.35
Formula:
C14H16N2O5S
Chemical Name:
5-{[2-(methoxymethyl)pyrrolidin-1-yl]sulfonyl}-2,3-dihydro-1H-indole-2,3-dione
Smiles :
COCC1CCCN1S(=O)(=O)C1=CC2=C(C=C1)NC(=O)C2=O
InChiKey:
SLQMNVJNDYLJSF-UHFFFAOYSA-N
InChi :
InChI=1S/C14H16N2O5S/c1-21-8-9-3-2-6-16(9)22(19,20)10-4-5-12-11(7-10)13(17)14(18)15-12/h4-5,7,9H,2-3,6,8H2,1H3,(H,15,17,18)
Purity:
≥98% (or refer to the Certificate of Analysis)
Shipping Condition:
Shipped under ambient temperature as non-hazardous chemical or refer to Certificate of Analysis
Storage Condition :
Dry, dark and -20 oC for 1 year or refer to the Certificate of Analysis.{{Menin-MLL inhibitor 21} medchemexpress|{Menin-MLL inhibitor 21} JAK/STAT Signaling|{Menin-MLL inhibitor 21} Technical Information|{Menin-MLL inhibitor 21} Description|{Menin-MLL inhibitor 21} manufacturer|{Menin-MLL inhibitor 21} Autophagy}
Shelf Life:
≥12 months if stored properly.
Stock Solution Storage:
0 – 4 oC for 1 month or refer to the Certificate of Analysis.
Additional information:
Caspase-3/7 inbibitor I is a potent, reversible, isatin sulfonamide-based inhibitor of caspase-3 (KI(app) = 60 nM) and caspase-7 (KI(app) = 170 nM). Is a weaker inhibitor of caspase-9 (Ki(app) = 3.1 mM). It Has only a trivial effect (Ki(app) >25 mM) on the activities of caspase-1, caspase-2, caspase-4, caspase-6, and caspase-8. It has been shown to inhibit apoptosis in camptothecin treated Jurkat cells (IC50 ~50 µM). Also it has been reported to inhibit apoptosis in chondrocytes (44% inhibition at 10 µM and 98% inhibition at 50 µM). Selectivity for caspases-3 and 7 involves unique hydrophobic residues in the S2 pocket surrounding the catalytic cysteine residue. In some systems inhibition of caspases-3 and -7 can prevent apoptosis and may therefore have important therapeutic implications. A potent, cell-permeable, and specific, reversible inhibitor of caspase-3 (Ki = 60 nM) and caspase-7 (Ki = 170 nM).{{Bromhexine} MedChemExpress|{Bromhexine} Anti-infection|{Bromhexine} Purity & Documentation|{Bromhexine} Formula|{Bromhexine} manufacturer|{Bromhexine} Epigenetic Reader Domain} |Product information|CAS Number: 220509-74-0|Molecular Weight: 324.PMID:25558565 35|Formula: C14H16N2O5S|Chemical Name: 5-{[2-(methoxymethyl)pyrrolidin-1-yl]sulfonyl}-2,3-dihydro-1H-indole-2,3-dione|Smiles: COCC1CCCN1S(=O)(=O)C1=CC2=C(C=C1)NC(=O)C2=O|InChiKey: SLQMNVJNDYLJSF-UHFFFAOYSA-N|InChi: InChI=1S/C14H16N2O5S/c1-21-8-9-3-2-6-16(9)22(19,20)10-4-5-12-11(7-10)13(17)14(18)15-12/h4-5,7,9H,2-3,6,8H2,1H3,(H,15,17,18)|Technical Data|Appearance: Solid Power|Purity: ≥98% (or refer to the Certificate of Analysis)|Shipping Condition: Shipped under ambient temperature as non-hazardous chemical or refer to Certificate of Analysis|Storage Condition: Dry, dark and -20 oC for 1 year or refer to the Certificate of Analysis.|Shelf Life: ≥12 months if stored properly.|Stock Solution Storage: 0 – 4 oC for 1 month or refer to the Certificate of Analysis.|Drug Formulation: To be determined|HS Tariff Code: 382200|Products are for research use only. Not for human use.|
