Summary
IMPPAT Phytochemical identifier: IMPHY000418
Phytochemical name: Isocelosianin II
Synonymous chemical names:isocelosianin
External chemical identifiers:CID:101105494
Chemical structure information
SMILES:
OC[C@H]1O[C@@H](Oc2cc3C[C@@H](N(c3cc2O)/C=C/C2=CC(=N[C@@H](C2)C(=O)O)C(=O)O)C(=O)O)[C@@H]([C@H]([C@@H]1O)O)O[C@@H]1O[C@H](C(=O)O)[C@H]([C@@H]([C@H]1OC(=O)/C=C/c1ccc(c(c1)OC)O)O)OInChI:
InChI=1S/C40H42N2O22/c1-59-24-10-15(2-4-22(24)44)3-5-27(46)62-33-31(50)30(49)32(38(57)58)63-40(33)64-34-29(48)28(47)26(14-43)61-39(34)60-25-12-17-11-21(37(55)56)42(20(17)13-23(25)45)7-6-16-8-18(35(51)52)41-19(9-16)36(53)54/h2-8,10,12-13,19,21,26,28-34,39-40,43-45,47-50H,9,11,14H2,1H3,(H,51,52)(H,53,54)(H,55,56)(H,57,58)/b5-3+,7-6+/t19-,21+,26+,28+,29-,30-,31-,32-,33+,34+,39+,40-/m0/s1InChIKey:
OCHDWFBTRVNZFQ-HICRZIJPSA-NDeepSMILES:
OC[C@H]O[C@@H]OcccC[C@@H]Nc5cc9O))))/C=C/C=CC=N[C@@H]C6)C=O)O))))C=O)O))))))))C=O)O))))))))[C@@H][C@H][C@@H]6O))O))O[C@@H]O[C@H]C=O)O))[C@H][C@@H][C@H]6OC=O)/C=C/cccccc6)OC)))O))))))))))O))OFunctional groups:
CC(=O)O, CO, CO[C@H](C)OC, c/C=C/C(=O)OC, cN(C)/C=C/C1=CC(C(=O)O)=NCC1, cO, cOC, cO[C@@H](C)OC
Molecular scaffolds
Scaffold Graph/Node/Bond level:
O=C(C=Cc1ccccc1)OC1CCCOC1OC1CCCOC1Oc1ccc2c(c1)CCN2C=CC1=CC=NCC1Scaffold Graph/Node level:
OC(CCC1CCCCC1)OC1CCCOC1OC1CCCOC1OC1CCC2C(CCN2CCC2CCNCC2)C1Scaffold Graph level:
CC(CCC1CCCCC1)CC1CCCCC1CC1CCCCC1CC1CCC2C(CCC3CCCCC3)CCC2C1
Chemical classification
ClassyFire Kingdom: Organic compoundsClassyFire Superclass: Organic acids and derivativesClassyFire Class: Carboxylic acids and derivatives
ClassyFire Subclass: Pentacarboxylic acids and derivatives
NP Classifier Biosynthetic pathway: Alkaloids
NP Classifier Superclass: Tyrosine alkaloids
NP Classifier Class: Betalain alkaloids
NP-Likeness score: 1.343
Chemical structure download