Drug Information
Drug General Information | |||||
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Drug ID |
D0Z0AM
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Former ID |
DNCL001780
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Drug Name |
PSI-697
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Drug Type |
Small molecular drug
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Indication | Atherosclerosis; Thrombosis [ICD9: 414.0, 440, 437.6, 453, 671.5, 671.9; ICD10:I70, I80-I82] | Phase 1 | [1] | ||
Company |
Pfizer
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Structure |
![]() |
Download2D MOL |
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Formula |
C21H18ClNO3
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PubChem Compound ID | |||||
Target and Pathway | |||||
Target(s) | P-selectin | Target Info | Inhibitor | [2] | |
KEGG Pathway | Cell adhesion molecules (CAMs) | ||||
Malaria | |||||
Staphylococcus aureus infection | |||||
Pathway Interaction Database | IL4-mediated signaling events | ||||
amb2 Integrin signaling | |||||
Reactome | Platelet degranulation | ||||
Cell surface interactions at the vascular wall | |||||
WikiPathways | Human Complement System | ||||
Spinal Cord Injury | |||||
Cell surface interactions at the vascular wall | |||||
References | |||||
REF 1 | ClinicalTrials.gov (NCT00367692) Study Evaluating PSI-697 in Patients With Scleritis. U.S. National Institutes of Health. | ||||
REF 2 | Effect of PSI-697, a novel P-selectin inhibitor, on platelet-monocyte aggregate formation in humans. J Am Heart Assoc. 2013 Jan 28;2(1):e006007. | ||||
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