| Bioactivity | Fosinopril (SQ28555 free acid) is the ester prodrug of angiotensin-converting enzyme (ACE) inhibitor with an IC50 value of 0.18 μM. Fosinopril demonstrates a non-competitive inhibition effect on ACE activity with an Ki value of 1.675 μM[1][2]. |
| Invitro | Fosinopril (0-100μM; 30 min) partially inhibits the cosedimentation of liposomes and recombinant LPLA2[1].Fosinopril (250 nM) shows no inhibition of the soluble esterase activity of LPLA2[1].Fosinopril (0.372, 0.744, 1.116 μM) displays a non-competitive inhibition effect on ACE activity with an Ki value of 1.675 μM[2]. |
| Name | Fosinopril |
| CAS | 98048-97-6 |
| Formula | C30H46NO7P |
| Molar Mass | 563.66 |
| Transport | Room temperature in continental US; may vary elsewhere. |
| Storage | Please store the product under the recommended conditions in the Certificate of Analysis. |
Fosinopril
CAS: 98048-97-6 F: C30H46NO7P W: 563.66
Fosinopril (SQ28555 free acid) is the ester prodrug of angiotensin-converting enzyme (ACE) inhibitor with an IC50 value
Data collection：peptidedb@qq.com
This product is for research use only, not for human use. We do not sell to patients.