Compound
all-trans-4-hydroxyretinol
No description recorded for this entry yet. Everything this graph holds about all-trans-4-hydroxyretinol is below.
Structure
- Class
- Organic compound
- Formula
- C20H30O2
- Mass
- 302.458 g/mol
- Charge
- 0
- InChIKey
- IOELQUUUYMBPSA-RMWYGNQTSA-N
- SMILES
- CC1=C(/C=C/C(C)=C/C=C/C(C)=C/CO)C(C)(C)CCC1O
- Look it up
- ChEBIBy InChIKey
Identity from ChEBI. Not evidence — none of it carries a grade.
What it touches on the way
A finding says all-trans-4-hydroxyretinol moved an endpoint. This is the biology in between: the proteins and reactions it runs through to get there. It is where to look for the two things a list of findings cannot answer — why a result might happen, and what else acts on the same machinery.
1 of these are proteins with a page of their own, and that is the door: a protein page says what else it carries, which is how one compound leads to the next.
Mechanistic reach
1 entity
1 entities reached, most connected first. Hub metabolites are excluded, so this is not a claim that the compound touches everything.
0 reported hops1 assembled from the scaffold
What the reference databases state
The section above shows paths a projection assembled. This is the reference layer itself, one step from all-trans-4-hydroxyretinol: what the cleared databases state it reacts with, is carried by, is converted to and takes part in, whether or not a projection has walked it yet.
Statements
1 statement
1 statement in 1 reference database name all-trans-4-hydroxyretinol — Rhea. Press a relation to see only its rows; every count is the rows behind it.
- all-trans-4-hydroxyretinol is metabolised by CYP27C1ProteinRhea RHEA:50300Inferred only
Other names
3 names
Every name this graph resolves to all-trans-4-hydroxyretinol. Searching any of them lands here.
- Also called
- 3-[(1E,3E,5E,7E)-9-hydroxy-3,7-dimethylnona-1,3,5,7-tetraenyl]-2,4,4-trimethylcyclohex-2-en-1-ol4-hydroxy-retinol
- Systematic name
- 4-hydroxyretinol