| Identification | Back Directory | [Name]
I-SAP | [CAS]
133538-58-6 | [Synonyms]
I-SAP
I SAP,ISAP
THROMBOXANE A2
SZNMERGTFJHNSM-JAWYFFTGSA-N
IODOPHENYL SULFONYL AMINO PINANE
7-(6,6-dimethyl-3-(4-iodobenzenesulfonylamino)bicyclo(3.1.1.)hept-2-yl)-5-heptenoic acid
[3S-[1alpha,3beta-5alpha]]-7-[3-[[(4-Ifodophenyl)sulfonyl]amino]-6,6-dimethylbicyclo[3.1.1]hept-2-yl]-5Z-heptenoic acid
[3S-[1ALPHA,2ALPHA,3BETA-5ALPHA]]-7-[3-[[(4-IODOPHENYL)SULFONYL]AMINO]-6,6-DIMETHYLBICYCLO[3.1.1]HEPT-2-YL]-5Z-HEPTENOIC ACID | [Molecular Formula]
C22H30INO4S | [MDL Number]
MFCD00216083 | [MOL File]
133538-58-6.mol | [Molecular Weight]
531.45 |
| Chemical Properties | Back Directory | [Boiling point ]
606.3±61.0 °C(Predicted) | [density ]
1.51±0.1 g/cm3(Predicted) | [storage temp. ]
Store at -20°C | [solubility ]
DMF: >50 mg/ml (from Pinane TXA2); DMSO: >25 mg/ml (from Pinane TXA2); Ethanol: >100 mg/ml (from Pinane TXA2); PBS pH 7.2: >100 μg/ml (from Pinane TXA2) | [pka]
4.76±0.10(Predicted) |
| Hazard Information | Back Directory | [Uses]
I-SAP is a radioiodinated TXA2/PGH2 receptor antagonist. The bind between I-SAP and the receptors, is inhibited by the histidine modifying reagent diethyl-pyrocarbonate (DEPC)[1][2]. | [IC 50]
TXA2 Receptor | [storage]
Store at -20°C | [References]
[1] Saussy DL Jr, et al. Binding of a novel radioiodinated thromboxane A2/prostaglandin H2 antagonist to guinea pig lung membranes. Eicosanoids. 1992;5(1):1-4. PMID:1419073
[2] Schr?r K, et al. Inhibition of ligand binding to thromboxane A2/prostaglandin H2 receptors by diethylpyrocarbonate. Protection by receptor ligands and reversal by hydroxylamine. Biochem Pharmacol. 1995 Mar 30;49(7):921-7. DOI:10.1016/0006-2952(95)00015-r |
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