Drug Information
| Drug General Information | Top | |||
|---|---|---|---|---|
| Drug ID |
D00GJZ
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| Former ID |
DNC002970
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| Drug Name |
N-Methylmesoporphyrin Containing Copper
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| Synonyms |
N-METHYLMESOPORPHYRIN CONTAINING COPPER
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| Drug Type |
Small molecular drug
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| Indication | Discovery agent [ICD-11: N.A.] | Investigative | [1] | |
| Structure |
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Download2D MOL |
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| Formula |
C35H39CuN4O4+
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| Canonical SMILES |
CCC1=C(C2=CC3=C(C(=C(N3C)C=C4C(=C(C(=N4)C=C5C(=C(C(=CC1=N2)[N-]5)C)CCC(=O)O)CCC(=O)O)C)C)CC)C.[Cu+2]
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| InChI |
1S/C35H40N4O4.Cu/c1-8-22-18(3)28-17-33-23(9-2)21(6)32(39(33)7)16-27-20(5)25(11-13-35(42)43)31(38-27)15-30-24(10-12-34(40)41)19(4)26(36-30)14-29(22)37-28;/h14-17H,8-13H2,1-7H3,(H3,36,37,38,40,41,42,43);/q;+2/p-1
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| InChIKey |
WLMGFVUEDVZKTK-UHFFFAOYSA-M
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| PubChem Compound ID | ||||
| PubChem Substance ID | ||||
| Target and Pathway | Top | |||
|---|---|---|---|---|
| Target(s) | Ferrochelatase (FECH) | Target Info | Inhibitor | [1] |
| BioCyc | Heme biosynthesis | |||
| Heme biosynthesis from uroporphyrinogen-III I | ||||
| KEGG Pathway | Porphyrin and chlorophyll metabolism | |||
| Metabolic pathways | ||||
| Panther Pathway | Heme biosynthesis | |||
| Pathwhiz Pathway | Porphyrin Metabolism | |||
| Pathway Interaction Database | HIF-1-alpha transcription factor network | |||
| WikiPathways | Heme Biosynthesis | |||
| Metabolism of porphyrins | ||||
| References | Top | |||
|---|---|---|---|---|
| REF 1 | How many drug targets are there Nat Rev Drug Discov. 2006 Dec;5(12):993-6. | |||
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