Drug Information
| Drug General Information | Top | |||
|---|---|---|---|---|
| Drug ID |
D0X5ZA
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| Former ID |
DNC002969
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| Drug Name |
N-Methylmesoporphyrin
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| Synonyms |
N-METHYLMESOPORPHYRIN; 3,3'-(8,13-diethyl-3,7,12,17,22-pentamethylporphyrin-2,18-diyl)dipropanoic acid; 3,3'-(8,13-diethyl-3,7,12,17,22-pentamethyl-22,24-dihydroporphyrin-2,18-diyl)dipropanoic acid; 21-Methylmesoporphyrin; AC1L9GRR; SCHEMBL505199; DB01911; J2.132.966E; 3,8,13,17,23-Pentamethyl-7,12-diethyl-21H,23H-porphyrin-2,18-dipropanoic acid; 3-[18-(2-carboxyethyl)-8,13-diethyl-3,7,12,17,22-pentamethyl-23H-porphyrin-2-yl]propanoic acid
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| Drug Type |
Small molecular drug
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| Indication | Discovery agent [ICD-11: N.A.] | Investigative | [1] | |
| Structure |
 |
Download2D MOL |
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| Formula |
C35H40N4O4
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| Canonical SMILES |
CCC1=C(C2=CC3=C(C(=C(N3C)C=C4C(=C(C(=N4)C=C5C(=C(C(=N5)C=C1N2)C)CCC(=O)O)CCC(=O)O)C)C)CC)C
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| InChI |
1S/C35H40N4O4/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/h14-17,37H,8-13H2,1-7H3,(H,40,41)(H,42,43)
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| InChIKey |
ZIBXESYSFXNOJI-UHFFFAOYSA-N
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| CAS Number |
CAS 142234-85-3
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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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