(Q27132635)

English

glutinol

chemical compound

3beta-hydroxy-D:B-friedoolean-5-ene
3beta-hydroxyglutin-5-ene
glutin-5-en-3beta-ol
5-Glutinen-3-ol
Glutinol
epi-Alnusenol

In more languages

default for all languages

No label defined

No description defined

Statements

type of chemical entity

0 references

glutinane triterpenoid

0 references

426.386±0 dalton

1 reference

language of work or name

glutinol (English)

7 October 2016

stereoisomer of

(3S,6aS,6aR,6bS,8aR,12aR,14aR,14bS)-4,4,6a,6b,8a,11,11,14a-octamethyl-1,2,3,6,6a,7,8,9,10,12,12a,13,14,14b-tetradecahydropicen-3-ol

2 references

based on heuristic

inferred from InChIKey

based on heuristic

inferred from InChI

2 references

based on heuristic

inferred from InChIKey

based on heuristic

inferred from InChI

(3S,6aR,6aS,6bS,8aS,12aR,14aS,14bS)-4,4,6a,6b,8a,11,11,14a-octamethyl-1,2,3,6,6a,7,8,9,10,12,12a,13,14,14b-tetradecahydropicen-3-ol

1 reference

based on heuristic

inferred from InChI

(3S,6aS,6aS,6bR,8aR,12aS,14aR,14bS)-4,4,6a,6b,8a,11,11,14a-octamethyl-1,2,3,6,6a,7,8,9,10,12,12a,13,14,14b-tetradecahydropicen-3-ol

1 reference

based on heuristic

inferred from InChI

chemical formula

C₃₀H₅₀O

1 reference

language of work or name

glutinol (English)

7 October 2016

canonical SMILES

CC1(CCC2(CCC3(C4CC=C5C(C4(CCC3(C2C1)C)C)CCC(C5(C)C)O)C)C)C

1 reference

language of work or name

glutinol (English)

7 October 2016

isomeric SMILES

C[C@@]12CC[C@@]3([C@H]4CC=C5[C@H]([C@@]4(CC[C@]3([C@@H]1CC(CC2)(C)C)C)C)CC[C@@H](C5(C)C)O)C

1 reference

language of work or name

glutinol (English)

7 October 2016

Buddleja globosa

1 reference

Ethnopharmacology of some Buddleja species

Euphorbia segetalis

2 references

Evaluation of the antiviral and antimicrobial activities of triterpenes isolated from Euphorbia segetalis

A Tetracyclic diterpene and triterpenes from euphorbia segetalis

Clausena excavata

1 reference

Chemical and antiplatelet aggregative investigation of the leaves of Clausena excavata

Hibiscus cannabinus

1 reference

Chemical composition of the light petroleum extract ofHibiscus cannabinus bark and core

Dalbergia sericea

1 reference

Triterpenoids and flavonoids of Dalbergia sericea bark

Euphorbia supina

1 reference

Obtusifoliol and related steroids from the whole herb of Euphorbia chamaesyce

Kalanchoe spathulata

1 reference

Triterpenoids and sterols of Kalanchoe spathulata

Syzygium formosanum

1 reference

Terpenoids of Syzygium formosanum

Uvaria scheffleri

2 references

(+/-)-Schefflone: a trimeric monoterpenoid from the root bark of Uvaria scheffleri

Schefflerin and isoschefflerin: Prenylated chalcones and other constituents of Uvaria scheffleri

Artocarpus integer

1 reference

A New Prenylated Flavone fromArtocarpus champeden

Volkameria inermis

1 reference

A steroidal glycoside from Clerodendron inerme

Diospyros maritima

1 reference

Bioactive Naphthoquinone Derivatives from Diospyros maritima BLUME.

Dorstenia bornimiana

1 reference

Styrenes from Dorstenia barnimiana

Euphorbia chamaesyce

1 reference

A 3,4-seco-8βH-fernadienoic acid and other constituents from Euphorbia chamaesyce

Euphorbia cyparissias

1 reference

Tetra-and Pentacyclic Triterpenoids from Epicuticular Wax of Euphorbia cyparissias L., Euphorbiaceae

Euphorbia piscatoria

1 reference

Tetra- and Pentacyclic Triterpenes from the Aerial Parts of Euphorbia piscatoria

Euphorbia portlandica

1 reference

Isoprenoid compounds from Euphorbia portlandica. X-ray structure of lupeportlandol, a new lupane triterpene

1 reference

Constituents of Ficus pumila Leaves.

Ficus sarmentosa var. thunbergii

1 reference

Triterpenoid Constituents of Ficus thunbergii.

Phyllostachys edulis

1 reference

Two lignan dimers from bamboo stems (Phyllostachys edulis)

Rhinacanthus nasutus

1 reference

A quinol and steroids from the leaves and stems of Rhinacanthus nasutus

Scoparia dulcis

4 references

Analgesic and antiinflammatory properties ofScoparia dulcis L. Extracts and glutinol in rodents

Scopadulciol, an Inhibitor of Gastric H+,K+-ATPhase from Scoparia dulcis, and Its Structure-Activity Relation-ships

A cytotoxic flavone from Scoparia dulcis L

Cytotoxic diterpenes from Scoparia dulcis

Sebastiania schottiana

2 references

Analgesic triterpenes from Sebastiania schottiana roots

Triterpenes from Sebastiania schottiana

Sideritis canariensis

1 reference

Diterpenes from Sideritis canariensis

Sideritis ferrensis

1 reference

Diterpenes from Sideritis ferrensis

1 reference

Antibacterial, antifungal and anthelmintic activities of root barks of Uvaria hookeri and Uvaria narum

2 references

Acetogenins from root bark of Uvaria narum

Antibacterial, antifungal and anthelmintic activities of root barks of Uvaria hookeri and Uvaria narum

Vahlia capensis

1 reference

A seco-olean-18-ene triterpene acid from Vahlia capensis

Acer mandshuricum

1 reference

Triterpene compounds isolated from Acer mandshuricum and their anti-inflammatory activity

Toxicodendron sylvestre

1 reference

The regulation of inflammatory cytokine secretion in macrophage cell line by the chemical constituents of Rhus sylvestris

Croton gratissimus

1 reference

Cembranolides from the leaves of Croton gratissimus.

Armillaria mellea

1 reference

Triterpene from Armillaria mellea

Artemisia igniaria

1 reference

Triterpenoids, p-coumaric acid esters and flavonoids from Artemisia igniaria

Diospyros sanza-minika

1 reference

Naphthoquinones and triterpenes from african Diospyros species

Erythrophleum fordii

1 reference

New diterpenoids and the bioactivity of Erythrophleum fordii

Garcinia cantleyana

1 reference

Cytotoxic caged-polyprenylated xanthonoids and a xanthone from Garcinia cantleyana

Maytenus salicifolia

1 reference

Constituents of fruit pulp of Maytenus salicifolia and complete 1D/2D NMR data of 3β-hydroxy-D:B-friedo-olean-5-ene

Rhododendron macrophyllum

1 reference

Revised structure of a steroid oxide from Rhododendron macrophyllum

Saussurea medusa

1 reference

Bioactive constituents from Chinese natural medicines. XV. Inhibitory effect on aldose reductase and structures of Saussureosides A and B from Saussurea medusa

Curio talinoides

1 reference

New Sesquiterpenes from Senecio species

Mallotus nudiflorus

1 reference

A Rare New Cleistanthane Diterpene from the Pericarp ofTrewia nudiflora

Garcinia cymosa

1 reference

(20R,23E)-Eupha-8,23-diene-3β,25-diol from Tripetalum cymosum

Vaccinium myrtillus

1 reference

Unusual p-Coumarates from the Stems of Vaccinium myrtillus

Kalanchoe integra

1 reference

Triterpenoids and sterols of Kalanchoe spathulata

1 reference

Antibacterial, antifungal and anthelmintic activities of root barks of Uvaria hookeri and Uvaria narum

Maclura tricuspidata

1 reference

Chemical Constituents Isolated from the Root Bark of Cudrania tricuspidata and Their Potential Neuroprotective Effects

1 reference

Garcinoic Acids and a Benzophenone Derivative from the Seeds of Garcinia kola and Their Antibacterial Activities against Oral Bacterial Pathogenic Organisms

Euphorbia maculata

1 reference

Obtusifoliol and related steroids from the whole herb of Euphorbia chamaesyce

Dolichousnea longissima

1 reference

Bioactive phenolic compounds from a medicinal lichen, Usnea longissima

Kalanchoe lanceolata

1 reference

Triterpenoids and sterols of Kalanchoe spathulata

Kalanchoe deficiens

1 reference

Triterpenoids and sterols of Kalanchoe spathulata

Identifiers

InChI=1S/C30H50O/c1-25(2)13-14-27(5)15-17-29(7)22-11-9-20-21(10-12-24(31)26(20,3)4)28(22,6)16-18-30(29,8)23(27)19-25/h9,21-24,31H,10-19H2,1-8H3/t21-,22+,23-,24+,27-,28+,29-,30+/m1/s1

1 reference

language of work or name

glutinol (English)

7 October 2016

HFSACQSILLSUII-ISSAZSKYSA-N

2 references

language of work or name

glutinol (English)

7 October 2016

ChEBI release 2020-09-01

CAS Registry Number

0 references

1 reference

language of work or name

(3S,6aS,6bR,8aR,12aR,12bS,14aR,14bS)-4,4,6b,8a,11,11,12b,14a-Octamethyl-1,2,3,4,6,6a,6b,7,8,8a,9,10,11,12,12a,12b,13,14,14a,14b-icosahydro-3-picenol (English)

7 October 2016

2 references

language of work or name

glutinol (English)

7 October 2016

matched by identifier from

HFSACQSILLSUII-ISSAZSKYSA-N

Reaxys registry number

2339451

1 reference

language of work or name

glutinol (English)

7 October 2016

mapping relation type

2 references

language of work or name

glutinol (English)

7 October 2016

matched by identifier from

International Chemical Identifier

InChI=1S/C30H50O/c1-25(2)13-14-27(5)15-17-29(7)22-11-9-20-21(10-12-24(31)26(20,3)4)28(22,6)16-18-30(29,8)23(27)19-25/h9,21-24,31H,10-19H2,1-8H3/t21-,22+,23-,24+,27-,28+,29-,30+/m1/s1

1 reference

language of work or name

GLUTINOL (English)

7 October 2016

UniChem compound ID

1 reference

DSSTox substance ID

2 references

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

matched by identifier from

HFSACQSILLSUII-ISSAZSKYSA-N

DSSTOX compound identifier

0 references

Natural Product Atlas ID

2 references

based on heuristic

inferred from InChIKey

matched by identifier from

HFSACQSILLSUII-ISSAZSKYSA-N

Sitelinks

Wikipedia(0 entries)

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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