Summary

IMPPAT Phytochemical identifier: IMPHY010012

Phytochemical name: 1,3,5,6-Tetrahydroxy-2-methylanthracene-9,10-dione

Synonymous chemical names:
3-hydroxymorindone, morindone, 3-hydroxy

External chemical identifiers:
CID:86012754, SureChEMBL:SCHEMBL17867452, MolPort-046-790-362

---

Chemical structure information

SMILES:
Oc1ccc2c(c1O)C(=O)c1c(C2=O)c(O)c(c(c1)O)C

InChI:
InChI=1S/C15H10O6/c1-5-9(17)4-7-11(12(5)18)13(19)6-2-3-8(16)15(21)10(6)14(7)20/h2-4,16-18,21H,1H3

InChIKey:
JCZGUFVZKUDRMM-UHFFFAOYSA-N

DeepSMILES:
Occcccc6O))C=O)ccC6=O))cO)ccc6)O))C

Functional groups:
cC(c)=O, cO

---

Molecular scaffolds

Scaffold Graph/Node/Bond level:
O=C1c2ccccc2C(=O)c2ccccc21

Scaffold Graph/Node level:
OC1C2CCCCC2C(O)C2CCCCC12

Scaffold Graph level:
CC1C2CCCCC2C(C)C2CCCCC12

---

Chemical classification

ClassyFire Kingdom: Organic compounds

ClassyFire Superclass: Benzenoids

ClassyFire Class: Anthracenes

ClassyFire Subclass: Anthraquinones

NP Classifier Biosynthetic pathway: Polyketides

NP Classifier Superclass: Polycyclic aromatic polyketides

NP Classifier Class: Anthraquinones and anthrones

NP-Likeness score: 1.475

---

Chemical structure download