(Q27131918)

inferred from SMILES

mass

426.386166±0 dalton

1 reference

(3S,4aS,6aR,6aR,6bR,8aR,14aR,14bR)-4,4,6a,6b,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,6a,7,8,9,10,13,14,14a-tetradecahydropicen-3-ol

Germanicol (English)

7 October 2016

2 references

inferred from InChIKey

(3R,4aR,6aS,6aR,6bR,8aR,14aR,14bR)-4,4,6a,6b,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,6a,7,8,9,10,13,14,14a-tetradecahydropicen-3-ol

inferred from InChI

2 references

inferred from InChIKey

(3R,4aS,6aR,6aR,6bR,8aS,14aR,14bS)-4,4,6a,6b,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,6a,7,8,9,10,13,14,14a-tetradecahydropicen-3-ol

inferred from InChI

1 reference

inferred from InChI

chemical formula

C₃₀H₅₀O

1 reference

Germanicol (English)

7 October 2016

CC1(CCC2(CCC3(C(C2=C1)CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C)C)C

1 reference

Germanicol (English)

7 October 2016

C[C@@]12CC[C@@]3([C@@H](C1=CC(CC2)(C)C)CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)O)C)C)C

1 reference

Characterization of triterpene alcohols of seed oils from some species of theaceae, phytolaccaceae and sapotaceae

Germanicol (English)

7 October 2016

1 reference

Camellia japonica

2 references

Characterization of triterpene alcohols of seed oils from some species of theaceae, phytolaccaceae and sapotaceae

Triterpene alcohols from camellia and sasanqua oils and their anti-inflammatory effects

Phytolacca americana

1 reference

Characterization of triterpene alcohols of seed oils from some species of theaceae, phytolaccaceae and sapotaceae

Mangifera indica

1 reference

Sterols, methyl sterols, triterpene alcohols and fatty acids of the kernel fat of different malagasy mango(Mangifera indica) varieties

Marsypianthes chamaedrys

2 references

Molluscicidal constituents of Marsypianthes chamaedrys

Chamaedrydiol, an ursane triterpene from Marsypianthes chamaedrys

Koelpinia linearis

3 references

Koelpinin-A, B and C--three triterpenoids from Koelpinia linearis

Koelpinin-A, B and C--three triterpenoids from Koelpinia linearis

Koelpinin-A, B and C--three triterpenoids from Koelpinia linearis

Euphorbia pulcherrima

2 references

Chemical Investigation of Fruits of Poinsettia pulcherrima

Chemical Investigation of Fruits of Poinsettia pulcherrima

Camellia sasanqua

1 reference

Triterpene alcohols from camellia and sasanqua oils and their anti-inflammatory effects

Cnidoscolus urens

1 reference

Triterpenoids of Cnidosculus urens

Cuphea wrightii

1 reference

Triterpenes and flavonoid glycosides from Cuphea wrightii

Equisetum arvense

1 reference

Triterpenoids and sterols from three Millettia species

Euphorbia characias

1 reference

Triterpenoids in Epicuticular Waxes of Three European Euphorbia Species

Euphorbia nicaeensis

1 reference

Triterpenoids in Epicuticular Waxes of Three European Euphorbia Species

Euphorbia peplus

1 reference

Triterpenoids in Epicuticular Waxes of Three European Euphorbia Species

Euphorbia supina

1 reference

Triterpene constituents from Euphorbia supina

Festuca argentina

1 reference

Linear, steroidal, and triterpene esters, and steryl glycosides from Festuca argentina

Ixeris chinensis

3 references

Composite Constitute: Novel Triterpenoid,from Aerial Parts of Ixeris chinensis.

Composite Constituents: Thirty-Nine Triterpenoids Including Two Novel Compounds from Ixeris chinensis.

Composite Constituents: Thirty-Nine Triterpenoids Including Two Novel Compounds from Ixeris chinensis.

Lactuca saligna

1 reference

Triterpenes and Triterpene Esters from Lactuca Saligna

lettuce

1 reference

Occurrence of amyrenyl and germanicyl acetates as major amyrenyl and germanicyl compounds in Lactuca sativa L. tap root

Olea europaea

1 reference

Triterpene alcohols and sterols of Spanish olive oil

Picris hieracioides

2 references

Composite Constituents: Forty-Two Triterpenoids Including Eight Novel Compounds Isolated from Picris hieracioides subsp. japonica.

Composite Constituents: Forty-Two Triterpenoids Including Eight Novel Compounds Isolated from Picris hieracioides subsp. japonica.

Pistacia lentiscus

1 reference

Triterpenoids from gum mastic, the resin ofPistacia lentiscus

meadow clary

1 reference

A lupeol derivative from Salvia pratensis

Scorzonera cretica

1 reference

Three new dihydroisocoumarins from the Greek endemic species Scorzonera cretica

Sonchus asper

1 reference

Benzine Extract from Sonchus asper-A Rich Source of Pentacyclic Triterpenoids

Stevia alpina

1 reference

Guaianolides, heliangolides and other constituents from Stevia alpina

Trixis grisebachii

1 reference

Trixanolide and germacratriene derivatives from Trixis grisebachii

Trixis praestans

1 reference

Trixane derivatives from Trixis praestans

Vernonanthura brasiliana

2 references

Antiplasmodial Triterpene fromVernonia brasiliana

Antiplasmodial Triterpene fromVernonia brasiliana

Vernonia incana

1 reference

Glaucolides and related sesquiterpene lactones from Vernonia incana

Chrysolaena propinqua

1 reference

Glaucolides and related sesquiterpene lactones from Vernonia nudiflora and Chrysolaena propinqua

Vitis vinifera

1 reference

The main triterpene compounds of vine leaves and rachises

Barringtonia asiatica

1 reference

New triterpenes from Barringtonia asiatica.

Barringtonia racemosa

1 reference

Two New 18-en-Oleane Derivatives from Marine Mangrove Plant, Barringtonia Racemosa

Lactuca virosa

1 reference

75. The triterpene group. Part XI. The non-saponifiable matter of Lactucarium germanicum

Gelasia cretica

1 reference

Three new dihydroisocoumarins from the Greek endemic species Scorzonera cretica

Celastraceae

1 reference

Olean-18-ene triterpenoids from Celastraceae species inhibit HIV replication targeting NF-kB and Sp1 dependent transcription.

tomato

1 reference

Composition of the surface wax from tomatoes

Camellia oleifera

1 reference

Triterpene alcohols from camellia and sasanqua oils and their anti-inflammatory effects

Euphorbia maculata

1 reference

Triterpene constituents from Euphorbia supina

Monteverdia horrida

1 reference

Triterpenes from Maytenus horrida

Identifiers

InChI

InChI=1S/C30H50O/c1-25(2)15-16-27(5)17-18-29(7)20(21(27)19-25)9-10-23-28(6)13-12-24(31)26(3,4)22(28)11-14-30(23,29)8/h19-20,22-24,31H,9-18H2,1-8H3/t20-,22+,23-,24+,27-,28+,29-,30-/m1/s1

1 reference

Germanicol (English)

7 October 2016

2 references

Germanicol (English)

7 October 2016

ChEBI release 2020-09-01

2 references

germanicol (English)

7 October 2016

https://commonchemistry.cas.org/detail?cas_rn=465-02-1

9 April 2021

1 reference

germanicol (English)

7 October 2016

2 references

English

title

Germanicol (English)

retrieved

7 October 2016

Reaxys registry number

2063474

1 reference

germanicol (English)

7 October 2016

mapping relation type

2 references

English

title

germanicol (English)

retrieved

7 October 2016

International Chemical Identifier

InChI

InChI=1S/C30H50O/c1-25(2)15-16-27(5)17-18-29(7)20(21(27)19-25)9-10-23-28(6)13-12-24(31)26(3,4)22(28)11-14-30(23,29)8/h19-20,22-24,31H,9-18H2,1-8H3/t20-,22+,23-,24+,27-,28+,29-,30-/m1/s1

1 reference

GERMANICOL (English)

7 October 2016

2 references

inferred from InChIKey

1 reference

1 reference

DSSTOX compound identifier

0 references

2 references

Global Substance Registration System

UNII

7NEX9512DZ

English

title

GERMANICOL (English)

retrieved

7 October 2016