dammarenediol-II (Q27131867)

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chemical compound

dammar-24-ene-20(SS),3beta-diol
(20S)-dammarenediol
8-methyl-18-nor-lanost-24-ene-3beta,20-diol
8-methyl-18-nor-lanost-24-en-3beta,20-diol
(20S)-dammar-24-ene-3beta,20-diol
dammarenediol II
dammarenediol
dammar-24-ene-3beta,20-diol
3beta-glucodammar-24-ene-3,20-diol
3beta-Dammar-24-ene-3,20-diol

Language	Label	Description	Also known as
English	dammarenediol-II	chemical compound	dammar-24-ene-20(SS),3beta-diol (20S)-dammarenediol 8-methyl-18-nor-lanost-24-ene-3beta,20-diol 8-methyl-18-nor-lanost-24-en-3beta,20-diol (20S)-dammar-24-ene-3beta,20-diol dammarenediol II dammarenediol dammar-24-ene-3beta,20-diol 3beta-glucodammar-24-ene-3,20-diol 3beta-Dammar-24-ene-3,20-diol

Statements

type of chemical entity

0 references

1 reference

based on heuristic

inferred from SMILES

(3aR,3bR,5aR,7S,9aR,9bR)-1-[(2S)-2-hydroxy-6-methylhept-5-en-2-yl]-3a,3b,6,6,9a-pentamethyl-dodecahydro-1H-cyclopenta[a]phenanthren-7-ol

1 reference

based on heuristic

inferred from SMILES

dammarenediol 12-hydroxylase activity

1 reference

Gene Ontology release 2020-05-02

Rhea release 113

444.396731±0 dalton

1 reference

language of work or name

Dammarenediol II (English)

7 October 2016

stereoisomer of

(3S,5S,8R,9R,10R,13R,14R,17S)-17-[(2S)-2-hydroxy-6-methylhept-5-en-2-yl]-4,4,8,10,14-pentamethyl-2,3,5,6,7,9,11,12,13,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol

1 reference

based on heuristic

inferred from InChI

5alpha-Dammar-24-ene-3alpha,20-diol

1 reference

based on heuristic

inferred from InChI

(3S,5R,8R,9R,10R,13R,14S,17R)-17-[(2S)-2-hydroxy-6-methylhept-5-en-2-yl]-4,4,8,10,14-pentamethyl-2,3,5,6,7,9,11,12,13,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol

1 reference

based on heuristic

inferred from InChI

Dammarenediol-I

1 reference

based on heuristic

inferred from InChI

chemical formula

C₃₀H₅₂O₂

1 reference

language of work or name

Dammarenediol II (English)

7 October 2016

canonical SMILES

CC(=CCCC(C)(C1CCC2(C1CCC3C2(CCC4C3(CCC(C4(C)C)O)C)C)C)O)C

1 reference

language of work or name

Dammarenediol II (English)

7 October 2016

isomeric SMILES

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

1 reference

language of work or name

Dammarenediol II (English)

7 October 2016

Pouteria caimito

1 reference

Triterpenes of Pouteria torta (Sapotaceae)

Pistacia lentiscus

1 reference

Triterpenoids from gum mastic, the resin ofPistacia lentiscus

2 references

Dammarane triterpenes from the hypocotyls and fruits of Ceriops tagal

Dammarane triterpenes from the hypocotyls and fruits of Ceriops tagal

Dysoxylum macranthum

1 reference

Tirucallane triterpenes from Dysoxylum macranthum

Cowania mexicana

1 reference

Search for New Drugs of Plant Origin

Chrysanthemum morifolium

1 reference

Constituents of compositae plants. 2. Triterpene diols, triols, and their 3-o-fatty acid esters from edible chrysanthemum flower extract and their anti-inflammatory effects

Dysoxylum beddomei

1 reference

Beddomeilactone: a new triterpene from Dysoxylum beddomei

Dysoxylum malabaricum

2 references

Triterpenoids from Dysoxylum malabaricum

Triterpenoids from Dysoxylum malabaricum

1 reference

Triterpenoids from the resin of Shorea robusta

Trixis grisebachii

1 reference

Trixanolide and germacratriene derivatives from Trixis grisebachii

Trattinnickia burserifolia

1 reference

Phytochemistry of Trattinnickia burserifolia, T. rhoifolia, and Dacryodes hopkinsii: chemosystematic implications

Boswellia sacra

1 reference

Four new ursane-type triterpenes, olibanumols K, L, M, and N, from traditional egyptian medicine olibanum, the gum-resin of Boswellia carterii

Camellia japonica

1 reference

3-epicabraleahydroxylactone and other triterpenoids from camellia oil and their inhibitory effects on Epstein-Barr virus activation

1 reference

Dammarane derivatives in the fruit lipids of Olea madagascariensis

Ligustrum japonicum

1 reference

Chemical constituents from fruits of Ligustrum lucidum

Ligustrum lucidum

1 reference

Chemical constituents from fruits of Ligustrum lucidum

Dendranthema morifolium

1 reference

Constituents of compositae plants. 2. Triterpene diols, triols, and their 3-o-fatty acid esters from edible chrysanthemum flower extract and their anti-inflammatory effects

Aglaia abbreviata

1 reference

Triterpenoids from Aglaia abbreviata and their cytotoxic activities.

Purshia mexicana

1 reference

Search for New Drugs of Plant Origin

Aglaia elaeagnoidea

1 reference

Triterpenoids from Aglaia abbreviata and their cytotoxic activities.

Boswellia carteri

1 reference

Four new ursane-type triterpenes, olibanumols K, L, M, and N, from traditional egyptian medicine olibanum, the gum-resin of Boswellia carterii

Identifiers

InChI=1S/C30H52O2/c1-20(2)10-9-16-30(8,32)22-13-18-28(6)21(22)11-12-24-27(5)17-15-25(31)26(3,4)23(27)14-19-29(24,28)7/h10,21-25,31-32H,9,11-19H2,1-8H3/t21-,22+,23+,24-,25+,27+,28-,29-,30+/m1/s1

1 reference

language of work or name

Dammarenediol II (English)

7 October 2016

NLHQJXWYMZLQJY-TXNIMPHESA-N

2 references

language of work or name

Dammarenediol II (English)

7 October 2016

ChEBI release 2020-09-01

CAS Registry Number

2 references

language of work or name

dammarenediol-II (English)

7 October 2016

NLHQJXWYMZLQJY-TXNIMPHESA-N

CAS Common Chemistry

10 April 2021

https://commonchemistry.cas.org/detail?cas_rn=14351-29-2

1 reference

language of work or name

Dammar-24-ene-3beta,20-diol (English)

7 October 2016

2 references

language of work or name

Dammarenediol II (English)

7 October 2016

matched by identifier from

NLHQJXWYMZLQJY-TXNIMPHESA-N

Reaxys registry number

2511034

1 reference

language of work or name

dammarenediol-II (English)

7 October 2016

mapping relation type

2 references

language of work or name

dammarenediol-II (English)

7 October 2016

matched by identifier from

International Chemical Identifier

InChI=1S/C30H52O2/c1-20(2)10-9-16-30(8,32)22-13-18-28(6)21(22)11-12-24-27(5)17-15-25(31)26(3,4)23(27)14-19-29(24,28)7/h10,21-25,31-32H,9,11-19H2,1-8H3/t21-,22+,23+,24-,25+,27+,28-,29-,30+/m1/s1

1 reference

language of work or name

CHEMBL478945 (English)

7 October 2016

UniChem compound ID

1 reference

DSSTox substance ID

0 references

DSSTOX compound identifier

DTXCID501360636

0 references

Google Knowledge Graph ID

0 references

Sitelinks

Wikipedia(1 entry)

itwiki Dammarenediolo

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

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