(Q7828277)

Totarol (English)

7 October 2016

2 references

inferred from InChIKey

based on heuristic

inferred from InChI

chemical formula

C₂₀H₃₀O

1 reference

Totarol (English)

18 November 2016

CC(C)C1=C(C=CC2=C1CCC3C2(CCCC3(C)C)C)O

1 reference

Totarol (English)

18 November 2016

CC(C)C1=C(C=CC2=C1CC[C@@H]3[C@@]2(CCCC3(C)C)C)O

1 reference

Contribution to the Study of the Essential Oil of Thuja occidentalis L.

Totarol (English)

18 November 2016

1 reference

Thujopsis dolabrata

2 references

Diterpene production by callus of some plants belonging to cupressaceae.

Terpenoids from the seed of Thujopsis dolabrata var. Dolabrata

Chamaecyparis obtusa

1 reference

Diterpene production by callus of some plants belonging to cupressaceae.

Chamaecyparis pisifera

1 reference

Diterpene production by callus of some plants belonging to cupressaceae.

Juniperus communis

1 reference

Antimycobacterial terpenoids from Juniperus communis L. (Cuppressaceae).

Chamaecyparis formosensis

3 references

Terpenes and lignans from leaves of Chamaecyparis formosensis

Terpenes and lignans from leaves of Chamaecyparis formosensis

Terpenes and lignans from leaves of Chamaecyparis formosensis

Tetraclinis articulata

4 references

Diterpenoids from Tetraclinis articulata that inhibit various human leukocyte functions

Diterpenoids from Tetraclinis articulata that inhibit various human leukocyte functions

Diterpenoids from Tetraclinis articulata that inhibit various human leukocyte functions

The Chemistry of the Natural Order Cupressales. 42. Heartwood Constituents of Tetraclinis articulata (Vahl) Masters.

Apis mellifera

2 references

Characterization and antioxidant properties of six Algerian propolis extracts: ethyl acetate extracts inhibit myeloperoxidase activity

Terpenes with antimicrobial activity from Cretan propolis

Juniperus phoenicea

1 reference

Chemical compounds from Phoenician juniper berries (Juniperus phoenicea)

Cryptomeria japonica

2 references

Abietanes and kauranes from leaves of Cryptomeria japonica

Labdanes from Cryptomeria japonica

Dacrycarpus vieillardii

1 reference

Phenolic diterpenoids of podocarpus ferrugineus and other podocarps

Nageia wallichiana

1 reference

Extractives of Decussocarpus wallichianus

Juniperus chinensis

8 references

Diterpenes from leaves of Juniperus chinensis

Terpenes from heartwood of Juniperus chinensis

Diterpenes from the bark of Juniperus chinensis

Three New Diterpenes, 1,3-Dioxototarol, Isototarolenone, and 1-Oxo-3.BETA.-hydroxytotarol, from the Roots of Juniperus chinensis LINN.

Terpenes from heartwood of Juniperus chinensis

Diterpenes from leaves of Juniperus chinensis

Diterpenes from the bark of Juniperus chinensis

Three New Diterpenes, 1,3-Dioxototarol, Isototarolenone, and 1-Oxo-3.BETA.-hydroxytotarol, from the Roots of Juniperus chinensis LINN.

Juniperus formosana

1 reference

Five new compounds from the heartwood of Juniperus formosana Hayata.

Podocarpus affinis

2 references

Phenolic diterpenoids of podocarpus ferrugineus and other podocarps

Phenolic diterpenoids of podocarpus ferrugineus and other podocarps

Nageia nagi

4 references

Inhibition of lipid peroxidation by diterpenoid from Podocarpus nagi

Antibacterial activity of totarol and its potentiation

Antioxidative action of diterpenoids from Podocarpus nagi

Two nor-diterpene dilactones from Podocarpus nagi

Schistochila acuminata

1 reference

A cyclic peroxide of clerodenoic acid from the Taiwanese liverwort Schistochila acuminata

Thuja plicata

1 reference

Totarol, totaradiol and ferruginol: three diterpenes from Thuja plicata (Cupressaceae)

Thuja standishii

4 references

Anti-tumor promoting diterpenes from the stem bark of Thuja standishii (Cupressaceae).

Aromatase inhibitory activities of standishinal and the diterpenoids from the bark of Thuja standishii

Anti-tumor promoting diterpenes from the stem bark of Thuja standishii (Cupressaceae).

Diterpenes in the Essential Oil Extracted from the Leaf of Thuja Standishif Carriere

Callitropsis nootkatensis

1 reference

(+)-Totarol from Chamaecyparis nootkatensis and activity against Mycobacterium tuberculosis

Xanthocyparis nootkatensis

1 reference

(+)-Totarol from Chamaecyparis nootkatensis and activity against Mycobacterium tuberculosis

Juniperus rigida

1 reference

Diterpenes of Juniperus conferta

Retrophyllum minor

1 reference

Chemistry of the Podocarpaceae. XXVIII. Constituents of some Podocarpus and other species

Podocarpus totara

1 reference

Chemistry of the Podocarpaceae. XXVIII. Constituents of some Podocarpus and other species

Thujopsis dolabrata var. dolabrata

1 reference

Terpenoids from the seed of Thujopsis dolabrata var. Dolabrata

Cupressus sempervirens

1 reference

Sempervirol, a novel type of diterpene phenol

Platycladus orientalis

3 references

Diterpene production by callus of some plants belonging to cupressaceae.

Isolation and characterization of platelet-activating factor receptor binding antagonists from Biota orientalis

Identification and characterization of GABA(A) receptor modulatory diterpenes from Biota orientalis that decrease locomotor activity in mice.

Afrocarpus falcatus

1 reference

Phenolic diterpenoids of podocarpus ferrugineus and other podocarps

Podocarpus rumphii

1 reference

Phenolic diterpenoids of podocarpus ferrugineus and other podocarps

Retrophyllum comptonii

1 reference

Phenolic diterpenoids of podocarpus ferrugineus and other podocarps

Commons category

Totarol

0 references

Identifiers

InChI

InChI=1S/C20H30O/c1-13(2)18-14-7-10-17-19(3,4)11-6-12-20(17,5)15(14)8-9-16(18)21/h8-9,13,17,21H,6-7,10-12H2,1-5H3/t17-,20+/m0/s1

1 reference

Totarol (English)

18 November 2016

2 references

Totarol (English)

18 November 2016

ChEBI release 2020-09-01

CAS Registry Number

511-15-9

2 references

Global Substance Registration System

UNII

67NH2854WW

totarol (English)

18 November 2016

https://commonchemistry.cas.org/detail?cas_rn=511-15-9

10 April 2021

1 reference

(+)-Totarol (English)

18 November 2016

2 references

Totarol (English)

18 November 2016

ChEBI ID

69241

mapping relation type

2 references

TOTAROL (English)

18 November 2016

International Chemical Identifier

InChI

InChI=1S/C20H30O/c1-13(2)18-14-7-10-17-19(3,4)11-6-12-20(17,5)15(14)8-9-16(18)21/h8-9,13,17,21H,6-7,10-12H2,1-5H3/t17-,20+/m0/s1

1 reference

TOTAROL (English)

18 November 2016

2 references

inferred from InChIKey

splash10-0002-0900000000-43128d7f2a1ca5934467

1 reference

0 references

DSSTox substance ID

DTXSID9047752

2 references

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

DSSTOX compound identifier

0 references

0 references

1 reference

ECHA Substance Infocard database

ECHA Substance Infocard ID

100.151.658

27 December 2018

ECHA Substance Infocard ID

4bS-trans-8,8-Trimethyl-4b,5,6,7,8,8a,9,10-octahydro-1-isopropyl-phenanthren-2-ol (English)

quotation

CAS no.: 511-15-9 (English)

100.151.658

1 reference

ECHA Substance Infocard database

ECHA Substance Infocard ID

100.151.658

27 December 2018

Global Substance Registration System

4bS-trans-8,8-Trimethyl-4b,5,6,7,8,8a,9,10-octahydro-1-isopropyl-phenanthren-2-ol (English)

quotation

CAS no.: 511-15-9 (English)

0 references

1 reference

UNII

67NH2854WW

Global Substance Registration System

totarol (English)

18 November 2016

2 references

UNII

67NH2854WW

totarol (English)

18 November 2016