Name | Acutoside a |
Wikidata | Q27133812 |
Mol. formula | C42H68O13 |
CAS registry number | - |
Mol. weight | 780.9831 |
Temporary LOTUS id | LTS0110716 |
Name | Acutoside a |
Canonical SMILES | CC1(C)CC[C@]2(C(=O)O)CC[C@]3(C)C(=CC[C@@H]4[C@@]5(C)CC[C@H](O[C@@H]6O[C@H](CO)[C@@H](O)[C@H](O)[C@H]6O[C@@H]6O[C@H](CO)[C@@H](O)[C@H](O)[C@H]6O)C(C)(C)[C@@H]5CC[C@]43C)[C@@H]2C1 |
2D SMILES | CC1(C)CCC2(C(=O)O)CCC3(C)C(=CCC4C5(C)CCC(OC6OC(CO)C(O)C(O)C6OC6OC(CO)C(O)C(O)C6O)C(C)(C)C5CCC43C)C2C1 |
IUPAC name | (4aS,6aS,6bR,8aR,10S,12aR,12bR,14bS)-10-{[(2R,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}oxan-2-yl]oxy}-2,2,6a,6b,9,9,12a-heptamethyl-1,2,3,4,4a,5,6,6a,6b,7,8,8a,9,10,11,12,12a,12b,13,14b-icosahydropicene-4a-carboxylic acid |
InChI | InChI=1S/C42H68O13/c1-37(2)14-16-42(36(50)51)17-15-40(6)21(22(42)18-37)8-9-26-39(5)12-11-27(38(3,4)25(39)10-13-41(26,40)7)54-35-33(31(48)29(46)24(20-44)53-35)55-34-32(49)30(47)28(45)23(19-43)52-34/h8,22-35,43-49H,9-20H2,1-7H3,(H,50,51)/t22-,23+,24+,25-,26+,27-,28+,29+,30-,31-,32+,33+,34-,35-,39-,40+,41+,42-/m0/s1 |
InChIKey | LEQCLUFJRGKLOA-WLMDKFIXSA-N |
Deep SMILES | could not be computed |
Murcko Framework | C1=C2C3CCCCC3CCC2C4CCC5CCCCC5C4C1 |
Pathway | Superclass | Class |
Terpenoids | Triterpenoids | Oleanane triterpenoids |
Total atom number | 123 |
Heavy atom number | 55 |
Bond count | 61 |
Number of carbons | 42 |
Minimal number of rings | 7 |
Maximal number of rings | 16 |
NP-likeness score | 1.18 |
Alogp | 2.93 |
Alogp2 | 8.57 |
Apol | 129.6879 |
Bpol | 82.9601 |
EccentricConnectivityIndexDescriptor | 1885 |
FmfDescriptor | 0.6545 |
Fsp3 | 0.9286 |
FragmentComplexityDescriptor | 13671.13 |
PetitjeanNumber | 0.5 |
LipinskiRuleOf5Failures | 4 |
WienerPathNumber | 12192 |
Xlogp | 6.407 |
ZagrebIndex | 324 |
TopoPSA | 215.83 |