Descriptor English: | Coproporphyrinogens | ||||
Descriptor Spanish: |
Coproporfirinógenos
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Descriptor Portuguese: | Coproporfirinogênios | ||||
Descriptor French: | Coproporphyrinogènes | ||||
Tree number(s): |
D03.383.129.578.840.500.700.250 D03.633.400.909.500.700.250 D04.345.783.500.700.250 |
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RDF Unique Identifier: | https://id.nlm.nih.gov/mesh/D003305 | ||||
Scope note: | Porphyrinogens which are intermediates in the heme biosynthesis. They have four methyl and four propionic acid side chains attached to the pyrrole rings. Coproporphyrinogens I and III are formed in the presence of uroporphyrinogen decarboxylase from the corresponding uroporphyrinogen. They can yield coproporphyrins by autooxidation or protoporphyrin by oxidative decarboxylation. |
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Annotation: | intermediates in heme biosyn |
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Allowable Qualifiers: |
AD administration & dosage AE adverse effects AG agonists AI antagonists & inhibitors AN analysis BI biosynthesis BL blood CF cerebrospinal fluid CH chemistry CL classification CS chemical synthesis EC economics GE genetics HI history IM immunology IP isolation & purification ME metabolism PD pharmacology PH physiology PK pharmacokinetics PO poisoning RE radiation effects SD supply & distribution ST standards TO toxicity TU therapeutic use UR urine |
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Previous Indexing: |
Porphyrinogens (1975) Porphyrins (1971-1974) |
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Public MeSH Note: | 91; was see under PORPHYRINOGENS 1976-90 |
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History Note: | 91(76); was see under PORPHYRINOGENS 1976-90 |
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DeCS ID: | 3325 | ||||
Unique ID: | D003305 | ||||
Documents indexed in the Virtual Health Library (VHL): | Click here to access the VHL documents | ||||
Date Established: | 1991/01/01 | ||||
Date of Entry: | 1975/07/25 | ||||
Revision Date: | 2016/05/28 |
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CHEMICALS AND DRUGS
Heterocyclic Compounds [D03]Heterocyclic Compounds -
CHEMICALS AND DRUGS
Heterocyclic Compounds [D03]Heterocyclic Compounds -
CHEMICALS AND DRUGS
Polycyclic Compounds [D04]Polycyclic Compounds
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Coproporphyrinogens
- Preferred
Concept UI |
M0005158 |
Scope note | Porphyrinogens which are intermediates in the heme biosynthesis. They have four methyl and four propionic acid side chains attached to the pyrrole rings. Coproporphyrinogens I and III are formed in the presence of uroporphyrinogen decarboxylase from the corresponding uroporphyrinogen. They can yield coproporphyrins by autooxidation or protoporphyrin by oxidative decarboxylation. |
Preferred term | Coproporphyrinogens |
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