|
riboflavin |
|
CHEBI:17015 |
|
D-Ribitol in which the hydroxy group at position 5 is substituted by a 7,8-dimethyl-2,4-dioxo-3,4-dihydrobenzo[g]pteridin-10(2H)-yl moiety. It is a nutritional factor found in milk, eggs, malted barley, liver, kidney, heart, and leafy vegetables, but the richest natural source is yeast. The free form occurs only in the retina of the eye, in whey, and in urine; its principal forms in tissues and cells are as flavin mononucleotide and flavin-adenine dinucleotide. |
|
 
This entity has been manually annotated by the ChEBI Team.
|
|
CHEBI:45214, CHEBI:15044, CHEBI:27299, CHEBI:8843, CHEBI:529204
|
|
|
|
Molfile
XML
SDF
|
|
more structures >>
|
|
|
InChI=1S/C17H20N4O6/c1- 7- 3- 9- 10(4- 8(7) 2) 21(5- 11(23) 14(25) 12(24) 6- 22) 15- 13(18- 9) 16(26) 20- 17(27) 19- 15/h3- 4,11- 12,14,22- 25H,5- 6H2,1- 2H3,(H,20,26,27) /t11- ,12+,14- /m0/s1 |
AUNGANRZJHBGPY-SCRDCRAPSA-N |
Cc1cc2nc3c(nc(=O)[nH]c3=O)n(C[C@H](O)[C@H](O)[C@H](O)CO)c2cc1C |
|
Mus musculus
(NCBI:txid10090)
|
Source: BioModels - MODEL1507180067
See:
PubMed
|
Escherichia coli
(NCBI:txid562)
|
See:
PubMed
|
Escherichia coli metabolite
Any bacterial metabolite produced during a metabolic reaction in Escherichia coli.
mouse metabolite
Any mammalian metabolite produced during a metabolic reaction in a mouse (Mus musculus).
cofactor
An organic molecule or ion (usually a metal ion) that is required by an enzyme for its activity. It may be attached either loosely (coenzyme) or tightly (prosthetic group).
food colouring
A food additive that imparts colour to food. In European countries, E-numbers for permitted food colours are from E 100 to E 199, divided into yellows (E 100-109), oranges (E 110-119), reds (E 120-129), blues and violets (E 130-139), greens (E 140-149), browns and blacks (E 150-159), and others (E 160-199).
B vitamin
A role played by any of the group of eight water-soluble vitamins originally thought to be a single compound (vitamin B). The group comprises of vitamin B1, B2, B3, B5, B6, B7, B9, and B12 (Around 20 other compounds were once thought to be B vitamins but are no longer classified as such). B vitamins play important roles in cell metabolism.
metabolite
Any intermediate or product resulting from metabolism. The term 'metabolite' subsumes the classes commonly known as primary and secondary metabolites.
|
|
photosensitizing agent
A chemical compound that can be excited by light of a specific wavelength and subsequently transfer energy to a chosen reactant. This is commonly molecular oxygen within a cancer tissue, which is converted to (highly rective) singlet state oxygen. This rapidly reacts with any nearby biomolecules, ultimately killing the cancer cells.
food colouring
A food additive that imparts colour to food. In European countries, E-numbers for permitted food colours are from E 100 to E 199, divided into yellows (E 100-109), oranges (E 110-119), reds (E 120-129), blues and violets (E 130-139), greens (E 140-149), browns and blacks (E 150-159), and others (E 160-199).
B vitamin
A role played by any of the group of eight water-soluble vitamins originally thought to be a single compound (vitamin B). The group comprises of vitamin B1, B2, B3, B5, B6, B7, B9, and B12 (Around 20 other compounds were once thought to be B vitamins but are no longer classified as such). B vitamins play important roles in cell metabolism.
|
|
View more via ChEBI Ontology
5- deoxy- 5- (7,8- dimethyl- 2,4- dioxo- 3,4- dihydrobenzo[g]pteridin- 10(2H)- yl)- D- ribitol
|
riboflavin
|
ChemIDplus
|
riboflavina
|
ChemIDplus
|
riboflavine
|
ChemIDplus
|
riboflavinum
|
ChemIDplus
|
1-deoxy-1-(7,8-dimethyl-2,4-dioxo-3,4-dihydrobenzo[g]pteridin-10(2H)-yl)pentitol
|
NIST Chemistry WebBook
|
6,7-dimethyl-9-D-ribitylisoalloxazine
Note: (2004-06-30) Uses obsolete isoalloxazine skeletal numbering system. |
|
ChemIDplus
|
7,8- dimethyl- 10- (D- ribo- 2,3,4,5- tetrahydroxypentyl)benzo[g]pteridine- 2,4(3H,10H)- dione
|
ChEBI
|
7,8-dimethyl-10-(D-ribo-2,3,4,5-tetrahydroxypentyl)isoalloxazine
|
ChemIDplus
|
7,8-Dimethyl-10-ribitylisoalloxazine
|
KEGG COMPOUND
|
E101
|
ChEBI
|
Lactoflavin
|
KEGG COMPOUND
|
riboflavin
|
ChEMBL
|
Riboflavin
|
KEGG COMPOUND
|
RIBOFLAVINE
|
PDBeChem
|
Vitamin B2
|
KEGG COMPOUND
|
vitamin B2
|
ChEBI
|
vitamin G
|
DrugBank
|
2834
|
DrugCentral
|
C00001552
|
KNApSAcK
|
C00255
|
KEGG COMPOUND
|
D00050
|
KEGG DRUG
|
DB00140
|
DrugBank
|
HMDB0000244
|
HMDB
|
LSM-4084
|
LINCS
|
RBF
|
PDBeChem
|
Riboflavin
|
Wikipedia
|
RIBOFLAVIN
|
MetaCyc
|
US2807611
|
Patent
|
US2876169
|
Patent
|
View more database links |
83-88-5
|
CAS Registry Number
|
KEGG COMPOUND
|
83-88-5
|
CAS Registry Number
|
NIST Chemistry WebBook
|
83-88-5
|
CAS Registry Number
|
ChemIDplus
|
97831
|
Reaxys Registry Number
|
Reaxys
|
97831
|
Beilstein Registry Number
|
Beilstein
|
16658098
|
PubMed citation
|
Europe PMC
|
22770225
|
PubMed citation
|
Europe PMC
|
24643482
|
PubMed citation
|
Europe PMC
|
25108762
|
PubMed citation
|
Europe PMC
|
|