Corrin

Corrin

Identifiers
CAS Number	262-76-0 Y
3D model (JSmol)	Interactive image
ChEBI	CHEBI:33221 Y
ChemSpider	16736705 Y
PubChem CID	6438343
UNII	288E04GRMT Y
CompTox Dashboard (EPA)	DTXSID70893668
InChI InChI=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- Y Key: WUPRCGRRQUZFAB-DEGKJRJSSA-N Y 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- Key: WUPRCGRRQUZFAB-DEGKJRJSBL
SMILES N=1C=4CCC=1\C=C2/NC(CC2)C\5CC/C(C=C3\CC/C(=N3)/C=4)=N/5
Properties
Chemical formula	C19H22N4
Molar mass	306.40478
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Y verify (what is YN ?) Infobox references

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".^[1]

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

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.^[2] Both feature four pyrrole-like subunits organized into rings. Corrins have a central 15-membered C₁₁N₄ ring whereas porphryins have an interior 16-membered C₁₂N₄ 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.

• Kieninger, Christoph; Deery, Evelyne; Lawrence, Andrew D.; Podewitz, Maren; Wurst, Klaus; Nemoto‐Smith, Emi; Widner, Florian J.; Baker, Joseph A.; Jockusch, Steffen; Kreutz, Christoph R.; Liedl, Klaus R.; Gruber, Karl; Warren, Martin J.; Kräutler, Bernhard (29 July 2019). "The Hydrogenobyric Acid Structure Reveals the Corrin Ligand as an Entatic State Module Empowering B 12 Cofactors for Catalysis". Angewandte Chemie International Edition. 58 (31): 10756–10760. doi:10.1002/anie.201904713. PMC 6771967. PMID 31115943.