(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 (8 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 chemical structure is recorded as Phycourobilin.png[4].
- (4S,10Z,16R)-phycourobilin's CAS Registry Number is recorded as 61932-71-6[5].
- (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[6].
- (4S,10Z,16R)-phycourobilin's InChI is recorded as InChI=1S/C33H42N4O6/c1-7-20-19(6)32(42)37-27(20)14-25-18(5)23(10-12-31(40)41)29(35-25)15-28-22(9-11-30(38)39)17(4)24(34-28)13-26-16(3)21(8-2)33(43)36-26/h15,26-27,35H,7-14H2,1-6H3,(H,36,43)(H,37,42)(H,38,39)(H,40,41)/b28-15-/t26-,27+/m1/s1[7].
- (4S,10Z,16R)-phycourobilin's InChIKey is recorded as KDCCOOGTVSRCHX-YYVBKQGDSA-N[8].
- (4S,10Z,16R)-phycourobilin's chemical formula is recorded as C₃₃H₄₂N₄O₆[9].
- (4S,10Z,16R)-phycourobilin's subclass of is recorded as heterocyclic compound[10].
- (4S,10Z,16R)-phycourobilin's Commons category is recorded as Phycourobilin[11].
- (4S,10Z,16R)-phycourobilin's has part is recorded as carbon[12].
- (4S,10Z,16R)-phycourobilin's PDB structure ID is recorded as 5B13[13].
- (4S,10Z,16R)-phycourobilin's PDB structure ID is recorded as 1EYX[14].
- (4S,10Z,16R)-phycourobilin's PDB structure ID is recorded as 1B8D[15].
- (4S,10Z,16R)-phycourobilin's PDB structure ID is recorded as 1LIA[16].
- (4S,10Z,16R)-phycourobilin's PDB structure ID is recorded as 2VJH[17].
- (4S,10Z,16R)-phycourobilin's Freebase ID is recorded as /m/02wbbk6[18].
- (4S,10Z,16R)-phycourobilin's ChemSpider ID is recorded as 4451232[19].
- (4S,10Z,16R)-phycourobilin's PubChem CID is recorded as 5289229[20].
- (4S,10Z,16R)-phycourobilin's ChEBI ID is recorded as 45097[21].
- (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[22].
- (4S,10Z,16R)-phycourobilin's mass is recorded as {'unit': 'Q483261', 'amount': '+590.31'}[23].
- (4S,10Z,16R)-phycourobilin's SureChEMBL ID is recorded as 1505660[24].
- (4S,10Z,16R)-phycourobilin's DSSTox substance ID is recorded as DTXSID80905084[25].
- (4S,10Z,16R)-phycourobilin's stereoisomer of is recorded as (+)-urobilin[26].
- (4S,10Z,16R)-phycourobilin's stereoisomer of is recorded as (-)-urobilin[27].
Why It Matters
(4S,10Z,16R)-phycourobilin ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (8 views/month).[2] (4S,10Z,16R)-phycourobilin has Wikipedia articles in 5 language editions, a strong signal of global cultural recognition.[28]