ITCMDBv1
IngredientID 26875

Mussaendoside g

C66H105NO27

Back to Browse

Relationship Network

Interactive first-hop connections across herbs, ingredients, formulas, targets, diseases, symptoms, syndromes, evidence, and monographs.

Click a node to open it in a new tab
Herb: 1Ingredient: 1Links: 1
Arranging relationship network...

Record Fields

Scalar fields from the final ingredient record.

Ingredient Id
26875
Core Entity Id
33064
Source Entity Count
1
Preferred Name
Mussaendoside g
Name En
Pubchem Id
101992967
Smiles Canonical
CC1C(OC(=O)C1NC(=O)C(=CC=CC(C)C2CCC3(C2(CCC45C3CCC6C4(C5)CCC(C6(C)C)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)C)O)O)O)O)OC9C(C(C(C(O9)COC1C(C(C(C(O1)CO)O)O)O)O)O)OC1C(C(C(C(O1)C)O)O)O)C)C)C)C
Molecular Formula
C66H105NO27
Molecular Weight
1344.5460
Inchikey
NJMKFBJXWPURTF-NZXFVVEUSA-N
Inchi
InChI=1S/C66H105NO27/c1-26(12-11-13-27(2)55(82)67-39-28(3)29(4)85-56(39)83)32-16-18-64(10)37-15-14-36-62(7,8)38(17-19-65(36)25-66(37,65)21-20-63(32,64)9)91-60-54(51(81)52(34(23-69)89-60)92-58-49(79)44(74)40(70)30(5)86-58)94-61-53(93-59-50(80)45(75)41(71)31(6)87-59)47(77)43(73)35(90-61)24-84-57-48(78)46(76)42(72)33(22-68)88-57/h11-13,26,28-54,57-61,68-81H,14-25H2,1-10H3,(H,67,82)/b12-11+,27-13+/t26-,28?,29?,30+,31+,32-,33-,34-,35-,36+,37+,38+,39?,40+,41+,42-,43-,44-,45-,46+,47+,48-,49-,50-,51+,52-,53-,54-,57-,58+,59+,60+,61+,63-,64+,65-,66+/m1/s1
Isomeric Smiles
C[C@H]1[C@@H]([C@H]([C@H]([C@@H](O1)O[C@@H]2[C@H](O[C@H]([C@@H]([C@H]2O)O[C@H]3[C@@H]([C@H]([C@@H]([C@H](O3)CO[C@H]4[C@@H]([C@H]([C@@H]([C@H](O4)CO)O)O)O)O)O)O[C@H]5[C@@H]([C@@H]([C@H]([C@@H](O5)C)O)O)O)O[C@H]6CC[C@]78C[C@]79CC[C@@]1([C@H](CC[C@]1([C@@H]9CC[C@H]8C6(C)C)C)[C@H](C)/C=C/C=C(\C)/C(=O)NC1C(C(OC1=O)C)C)C)CO)O)O)O
Cas Id
Ob Score
Mol Logp
-1.8326
Num H Donors
15
Num H Acceptors
27
Num Rotatable Bonds
18
Drug Likeness
0.0310
Polar Surface Area
Molecular Volume
Alogp

Names

Preferred names, aliases, and source labels retained in the final schema.

Name
Mussaendoside g
Role
preferred
Source
itcmdb_public
Preferred
Yes
Name
Mussaendoside g
Role
preferred
Source
HERB_v2
Preferred
Yes
Name
mussaendoside G
Role
preferred
Source
TCMBank
Preferred
Yes

Cross References

Trusted external identifiers retained for this final record.

Herb
HBIN036023
Tcmid
39934
Pub Chem
101992967
Tcmbank
TCMBANKIN031959

Attributes

Merged source attributes and domain-specific metadata.

In Ch I
InChI=1S/C66H105NO27/c1-26(12-11-13-27(2)55(82)67-39-28(3)29(4)85-56(39)83)32-16-18-64(10)37-15-14-36-62(7,8)38(17-19-65(36)25-66(37,65)21-20-63(32,64)9)91-60-54(51(81)52(34(23-69)89-60)92-58-49(79)44(74)40(70)30(5)86-58)94-61-53(93-59-50(80)45(75)41(71)31(6)87-59)47(77)43(73)35(90-61)24-84-57-48(78)46(76)42(72)33(22-68)88-57/h11-13,26,28-54,57-61,68-81H,14-25H2,1-10H3,(H,67,82)/b12-11+,27-13+/t26-,28?,29?,30+,31+,32-,33-,34-,35-,36+,37+,38+,39?,40+,41+,42-,43-,44-,45-,46+,47+,48-,49-,50-,51+,52-,53-,54-,57-,58+,59+,60+,61+,63-,64+,65-,66+/m1/s1
Mol Wt
1344.545999999999
Smiles
CC1C(OC(=O)C1NC(=O)C(=CC=CC(C)C2CCC3(C2(CCC45C3CCC6C4(C5)CCC(C6(C)C)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)C)O)O)O)O)OC9C(C(C(C(O9)COC1C(C(C(C(O1)CO)O)O)O)O)O)OC1C(C(C(C(O1)C)O)O)O)C)C)C)C
Mol Log P
-1.832599999999992
In Ch Ikey
NJMKFBJXWPURTF-NZXFVVEUSA-N
Num Hdonors
15
Drug Likeness
0.031
Num Hacceptors
27
Isomeric Smiles
C[C@H]1[C@@H]([C@H]([C@H]([C@@H](O1)O[C@@H]2[C@H](O[C@H]([C@@H]([C@H]2O)O[C@H]3[C@@H]([C@H]([C@@H]([C@H](O3)CO[C@H]4[C@@H]([C@H]([C@@H]([C@H](O4)CO)O)O)O)O)O)O[C@H]5[C@@H]([C@@H]([C@H]([C@@H](O5)C)O)O)O)O[C@H]6CC[C@]78C[C@]79CC[C@@]1([C@H](CC[C@]1([C@@H]9CC[C@H]8C6(C)C)C)[C@H](C)/C=C/C=C(\C)/C(=O)NC1C(C(OC1=O)C)C)C)CO)O)O)O
Canonical Smiles
CC1C(OC(=O)C1NC(=O)C(=CC=CC(C)C2CCC3(C2(CCC45C3CCC6C4(C5)CCC(C6(C)C)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)C)O)O)O)O)OC9C(C(C(C(O9)COC1C(C(C(C(O1)CO)O)O)O)O)O)OC1C(C(C(C(O1)C)O)O)O)C)C)C)C
Molecular Weight
1344.5 g/mol
Molecular Formula
C66H105NO27
Molecular Formula
C66H105NO27
Num Rotatable Bonds
18