Corrin

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title: "Corrin" type: doc version: 1 created: 2026-02-28 author: "Wikipedia contributors" status: active scope: public tags: ["biomolecules", "tetrapyrroles", "metabolism", "macrocycles", "schiff-bases"] topic_path: "general/biomolecules" source: "https://en.wikipedia.org/wiki/Corrin" license: "CC BY-SA 4.0" wikipedia_page_id: 0 wikipedia_revision_id: 0

| verifiedrevid = 443543138 | ImageFile = Corrin.svg | ImageSize = 220px | IUPACName = (5Z,9Z,14Z)-2,3,7,8,12,13,17,18,19,22-Decahydro-1H-corrin | OtherNames = | Section1 = {{Chembox Identifiers | ChemSpiderID_Ref = | ChemSpiderID = 16736705 | InChIKey = WUPRCGRRQUZFAB-DEGKJRJSBL | StdInChI_Ref = | StdInChI = 1S/C19H22N4/c1-3-14-10-16-5-7-18(22-16)19-8-6-17(23-19)11-15-4-2-13(21-15)9-12(1)20-14/h9-11,18-19,22H,1-8H2/b12-9-,15-11-,16-10- | StdInChIKey_Ref = | StdInChIKey = WUPRCGRRQUZFAB-DEGKJRJSSA-N | CASNo_Ref = | CASNo=262-76-0 | UNII_Ref = | UNII = 288E04GRMT | PubChem=6438343 | InChI = 1/C19H22N4/c1-3-14-10-16-5-7-18(22-16)19-8-6-17(23-19)11-15-4-2-13(21-15)9-12(1)20-14/h9-11,18-19,22H,1-8H2/b12-9-,15-11-,16-10- | ChEBI_Ref = | ChEBI = 33221 | SMILES = N=1C=4CCC=1\C=C2/NC(CC2)C\5CC/C(C=C3\CC/C(=N3)/C=4)=N/5 | Section2 = {{Chembox Properties | Formula=C19H22N4 | MolarMass=306.40478 | Appearance= | Density= | MeltingPt= | BoilingPt= | Solubility= | Section3 = {{Chembox Hazards | MainHazards= | FlashPt= | AutoignitionPt = Corrin is a heterocyclic compound. Although not known to exist on its own, the molecule is of interest as the parent macrocycle related to the cofactor and chromophore in vitamin B12. Its name reflects that it is the "core" of vitamin B12 (cobalamins). Compounds with a corrin core are known as "corrins".

There are two chiral centres, which in natural compounds like cobalamin have the same stereochemistry.

Coordination chemistry

Main article: vitamin B12

Upon deprotonation, the corrinoid ring is capable of binding cobalt. In vitamin B12, the resulting complex also features a benzimidazole-derived ligand, and the sixth site on the octahedron serves as the catalytic center.

The corrin ring resembles the porphyrin ring. Both feature four pyrrole-like subunits organized into rings. Corrins have a central 15-membered ring whereas porphyrins have an interior 16-membered ring. All four nitrogen centers are linked by conjugation structure, with alternating double and single bonds. In contrast to porphyrins, corrins lack one of the carbon groups that link the pyrrole-like units into a fully conjugated structure. With a conjugated system that extends only 3/4 of the way around the ring, and does not include any of the outer edge carbons, corrins have a number of non-conjugated sp3 carbons, making them more flexible than porphyrins and not as flat. A third closely related biological structure, the chlorin ring system found in chlorophyll, is intermediate between porphyrin and corrin, having 20 carbons like the porphyrins and a conjugated structure extending all the way around the central atom, but with only 6 of the 8 edge carbons participating.

Corroles (octadehydrocorrins) are fully aromatic derivatives of corrins.

References

References

  1. https://pubchem.ncbi.nlm.nih.gov/compound/6438343#section=IUPAC-Name&fullscreen=true
  2. Nelson, D. L.; Cox, M. M. "Lehninger, Principles of Biochemistry" 3rd Ed. Worth Publishing: New York, 2000. {{ISBN. 1-57259-153-6.
  3. (2005). "Chemistry and Enzymology of Vitamin B12". Chemical Reviews.

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biomoleculestetrapyrrolesmetabolismmacrocyclesschiff-bases