lucidenic acid d (Q27896898)

Lucidenic acid D2 (English)

21 November 2016

canonical SMILES

CC(CCC(=O)O)C1CC(=O)C2(C1(C(C(=O)C3=C2C(=O)CC4C3(CCC(=O)C4(C)C)C)OC(=O)C)C)C

1 reference

Lucidenic acid D2 (English)

21 November 2016

isomeric SMILES

C[C@H](CCC(=O)O)[C@H]1CC(=O)[C@@]2([C@@]1([C@@H](C(=O)C3=C2C(=O)C[C@@H]4[C@@]3(CCC(=O)C4(C)C)C)OC(=O)C)C)C

1 reference

Anti-human immunodeficiency virus-1 protease activity of new lanostane-type triterpenoids from Ganoderma sinense

Lucidenic acid D2 (English)

21 November 2016

1 reference

Ganoderma lucidum

10 references

Ganoderic acid D, E, F, and H and lucidenic acid D, E, and F, new triterpenoids from Ganoderma lucidum.

Structures of new terpenoid constituents of Ganoderma lucidum (Fr.) KARST (Polyporaceae).

Constituents of the fungus Ganoderma lucidum (Fr.) Karst. I Structures of ganoderic acids C2, E, I, and K, lucidenic acid F and related compounds.

Constituents of the fungus Ganoderma lucidum (Fr.) Karst. II Structures of ganoderic acids F, G, and H, lucidenic acids D2 and E2, and related compounds.

New terpenoids from Ganoderma lucidum and their bitterness.

Lucidenic acids P and Q, methyl lucidenate P, and other triterpenoids from the fungus Ganoderma lucidum and their inhibitory effects on Epstein-Barr virus activation

Ganoderic acid D, E, F, and H and lucidenic acid D, E, and F, new triterpenoids from Ganoderma lucidum.

Lucidenic acids P and Q, methyl lucidenate P, and other triterpenoids from the fungus Ganoderma lucidum and their inhibitory effects on Epstein-Barr virus activation

Constituents of the fungus Ganoderma lucidum (Fr.) Karst. II Structures of ganoderic acids F, G, and H, lucidenic acids D2 and E2, and related compounds.

Analysis of triterpenoids in ganoderma lucidum using liquid chromatography coupled with electrospray ionization mass spectrometry

Ganoderma lucidum var. lucidum

1 reference

Analysis of triterpenoids in ganoderma lucidum using liquid chromatography coupled with electrospray ionization mass spectrometry

Identifiers

InChI

InChI=1S/C29H38O8/c1-14(8-9-21(34)35)16-12-20(33)29(7)22-17(31)13-18-26(3,4)19(32)10-11-27(18,5)23(22)24(36)25(28(16,29)6)37-15(2)30/h14,16,18,25H,8-13H2,1-7H3,(H,34,35)/t14-,16-,18+,25-,27+,28+,29+/m1/s1

1 reference

Lucidenic acid D2 (English)

21 November 2016

1 reference

Global Substance Registration System

Lucidenic acid D2 (English)

21 November 2016

2 references

UNII

4C2000605T

lucidenic acid d (English)

21 November 2016

https://commonchemistry.cas.org/detail?cas_rn=98665-16-8

8 April 2021

2 references

Lucidenic acid D2 (English)

21 November 2016

ChEBI ID

176197

mapping relation type

exact match

2 references

ChEBI release 2022-06-13

International Chemical Identifier

InChI

InChI=1S/C29H38O8/c1-14(8-9-21(34)35)16-12-20(33)29(7)22-17(31)13-18-26(3,4)19(32)10-11-27(18,5)23(22)24(36)25(28(16,29)6)37-15(2)30/h14,16,18,25H,8-13H2,1-7H3,(H,34,35)/t14-,16-,18+,25-,27+,28+,29+/m1/s1

1 reference

splash10-03r0-0000990000-66e5073784cef3bc7425

LUCIDENIC ACID D2 (English)

21 November 2016

1 reference

0 references

DSSTox substance ID

DTXSID50631520

2 references

Mapping file of InChIStrings, InChIKeys and DTXSIDs for the EPA CompTox Dashboard

DSSTOX compound identifier

0 references

0 references

2 references

inferred from InChIKey

UNII

4C2000605T

2 references

Global Substance Registration System

UNII

4C2000605T

lucidenic acid d (English)

21 November 2016

Natural Product Atlas ID

NPA029050

2 references

based on heuristic

inferred from InChIKey