Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C28H38N4O6 |
| Molecular Weight | 526.6245 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
COC(=O)C1=C(C)NC(C)=C(C1C2=CC(=CC=C2)[N+]([O-])=O)C(=O)OCC(C)(C)CN3CCN(CC=C)CC3
InChI
InChIKey=QBTSPDQKRVMTRU-UHFFFAOYSA-N
InChI=1S/C28H38N4O6/c1-7-11-30-12-14-31(15-13-30)17-28(4,5)18-38-27(34)24-20(3)29-19(2)23(26(33)37-6)25(24)21-9-8-10-22(16-21)32(35)36/h7-10,16,25,29H,1,11-15,17-18H2,2-6H3
DescriptionSources: http://www.chemdrug.com/article/8/3285/16420800.html
Sources: http://www.chemdrug.com/article/8/3285/16420800.html
Iganidipin is a new dihydropiridynic derivative of calcium antagonist. It is the only currently available calcium antagonist in the form of ophthalmic solution. Its topical administration increases ipsilateral optic nerve head blood flow in rabbits and monkeys and inhibits the contraction of blood vessels induced by endothelin -1. Iganidipin is also used for treat Angina pectoris and Hypertension.
Approval Year
Targets
| Primary Target | Pharmacology | Condition | Potency |
|---|---|---|---|
Target ID: CHEMBL2363032 Sources: http://www.ncbi.nlm.nih.gov/pubmed/7575741 |
Conditions
| Condition | Modality | Targets | Highest Phase | Product |
|---|---|---|---|---|
| Primary | Unknown Approved UseUnknown |
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| Primary | Unknown Approved UseUnknown |
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| Primary | Unknown Approved UseUnknown |
Sample Use Guides
In Vivo Use Guide
Sources: http://www.ncbi.nlm.nih.gov/pubmed/12601046
for rabbit: (14)C-iganidipine solution (0.03%, 30 microL) was instilled into one eye
Route of Administration:
Topical
In Vitro Use Guide
Sources: http://www.ncbi.nlm.nih.gov/pubmed/16413513
Iganidipine (0.01-1 microM) increased the retinal ganglion cells (RGC) viability
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NCI_THESAURUS |
C333
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100000083682
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C65885
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C108540
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119687-33-1
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SUB08127MIG
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7124
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CHEMBL2106330
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ACTIVE MOIETY
SALT/SOLVATE (PARENT)