Details
Stereochemistry | RACEMIC |
Molecular Formula | C20H35NOS |
Molecular Weight | 337.563 |
Optical Activity | ( + / - ) |
Defined Stereocenters | 2 / 2 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CCCCCCCCN[C@@H](C)[C@H](O)C1=CC=C(SC(C)C)C=C1
InChI
InChIKey=BFCDFTHTSVTWOG-PXNSSMCTSA-N
InChI=1S/C20H35NOS/c1-5-6-7-8-9-10-15-21-17(4)20(22)18-11-13-19(14-12-18)23-16(2)3/h11-14,16-17,20-22H,5-10,15H2,1-4H3/t17-,20-/m0/s1
Suloctidil is considered to be calcium antagonist. In addition to its vascular antispasmodic activity, suloctidil affects blood platelets and enhances brain energy metabolism. Suloctidil was being evaluated in many clinical trials for use in dementia and thrombotic disorders. Suloctidil induces hepatotoxicity.
Originator
Approval Year
Targets
Primary Target | Pharmacology | Condition | Potency |
---|---|---|---|
Target ID: GO:0005262 |
0.45 µM [Ki] | ||
Target ID: GO:0070527 |
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Target ID: CHEMBL2760 Sources: https://www.ncbi.nlm.nih.gov/pubmed/18027916 |
Conditions
Condition | Modality | Targets | Highest Phase | Product |
---|---|---|---|---|
Sources: https://www.ncbi.nlm.nih.gov/pubmed/2988158 |
Primary | Unknown Approved UseUnknown |
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Primary | Unknown Approved UseUnknown |
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Curative | Unknown Approved UseUnknown |
Sample Use Guides
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/3036152
Suloctidil (10 microM) stimulated the release of prostacyclin (PGI2) from the rabbit aorta, the dog vena cava and the dog portal vein, in vitro.
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Classification Tree | Code System | Code | ||
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WHO-VATC |
QC04AX19
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NCI_THESAURUS |
C29707
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WHO-ATC |
C04AX19
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2536
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CHEMBL588119
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D013468
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6604413
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C152466
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DB13340
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XV1N1XY17K
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100000082955
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3452
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m948
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SUB10752MIG
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Suloctidil
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DTXSID4045638
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54767-75-8
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259-332-1
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ACTIVE MOIETY
SALT/SOLVATE (PARENT)