(4S,10Z,16R)-phycourobilin
0 sources
(4S,10Z,16R)-phycourobilin
Summary
(4S,10Z,16R)-phycourobilin is a type of chemical entity[1]. (4S,10Z,16R)-phycourobilin ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (6 views/month).[2]
Key Facts
- (4S,10Z,16R)-phycourobilin's instance of is recorded as type of chemical entity[3].
- (4S,10Z,16R)-phycourobilin's canonical SMILES is recorded as CCC1=C(C(=O)NC1CC2=C(C(=C(N2)C=C3C(=C(C(=N3)CC4C(=C(C(=O)N4)CC)C)C)CCC(=O)O)CCC(=O)O)C)C[4].
- (4S,10Z,16R)-phycourobilin's chemical formula is recorded as C₃₃H₄₂N₄O₆[5].
- (4S,10Z,16R)-phycourobilin is a type of heterocyclic compound[6].
- (4S,10Z,16R)-phycourobilin's Commons category is recorded as Phycourobilin[7].
- (4S,10Z,16R)-phycourobilin comprises carbon[8].
- (4S,10Z,16R)-phycourobilin's isomeric SMILES is recorded as CCC1=C(C(=O)N[C@H]1CC2=C(C(=C(N2)/C=C\3/C(=C(C(=N3)C[C@@H]4C(=C(C(=O)N4)CC)C)C)CCC(=O)O)CCC(=O)O)C)C[9].
- (4S,10Z,16R)-phycourobilin's mass is recorded as {'unit': 'Q483261', 'amount': '+590.31'}[10].
- (4S,10Z,16R)-phycourobilin's stereoisomer of is recorded as (+)-urobilin[11].
- (4S,10Z,16R)-phycourobilin's stereoisomer of is recorded as (-)-urobilin[12].
Why It Matters
(4S,10Z,16R)-phycourobilin ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (6 views/month).[2] (4S,10Z,16R)-phycourobilin has Wikipedia articles in 5 language editions, a strong signal of global cultural recognition.[13]