manool (Q15726184)

inferred from SMILES

mass

290.261±0 dalton

1 reference

(3R)-5-[(1S,4aR,8aS)-5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]-3-methylpent-1-en-3-ol

Manool (English)

8 October 2016

2 references

2 references

(3S)-5-[(1S,4aR,8aS)-5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]-3-methylpent-1-en-3-ol

inferred from InChI

2 references

2 references

(3R)-5-[(1R,4aS,8aR)-5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]-3-methylpent-1-en-3-ol

1 reference

1 reference

1 reference

(3S)-5-[(1R,4aR,8aS)-5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]-3-methylpent-1-en-3-ol

1 reference

1 reference

C₂₀H₃₄O

1 reference

Manool (English)

8 October 2016

CC1(CCCC2(C1CCC(=C)C2CCC(C)(C=C)O)C)C

1 reference

Manool (English)

8 October 2016

C[C@]12CCCC([C@@H]1CCC(=C)[C@@H]2CC[C@](C)(C=C)O)(C)C

1 reference

The Volatile Terpenoids of Juniperus monticola f. monticola, f. compacta, and f. orizabensis

Manool (English)

8 October 2016

1 reference

Cedrus libani

2 references

Phytochemical analysis and in vitro evaluation of the biological activity against herpes simplex virus type 1 (HSV-1) of Cedrus libani A. Rich

The Volatiles of the Leaves and Wood of Lebanon Cedar (Cedrus libaniA. Rich) Aromatic Plants of the Holy Land and the Sinai. Part XIV

Salvia officinalis

4 references

Chemical constituents and antimicrobial activity of the ethanol extracts obtained from the flower, leaf and stem of Salvia officinalis L

Dalmatian Sage. Part 1. Differing Oil Yields and Compositions from Flowering and Non-Flowering Accessions

Carnosic acid 12-methyl ether-γ-lactone, a ferruginol-type diterpene from Salvia officinalis

A quinone methide from Salvia officinalis

Abies chensiensis

1 reference

Terpenoid Constituents ofAbies chensiensiswith Potential Anti-inflammatory Activity

Abies firma

2 references

Terpenoids from seeds of Abies firma

Triterpenes from the seed of Abies firma

Abies sachalinensis

1 reference

Occurrence of epijuvabione-type sesquiterpenoids in Abies sachalinensis

Halocarpus biformis

2 references

The Biosynthesis of Labdanoids. The Optical Purity of Naturally Occurring Manool and Abienol

Über den Diterpen-alkohol aus dem Holz von Dacrydium biforme (I. Mitteil.)

Erythroxylum pictum

1 reference

Diterpenes from the timber of Erythroxylum pictum

Hamamelis virginiana

1 reference

Study on the composition of the volatile fraction of Hamamelis virginiana

Leiocarpa leptolepis

1 reference

Azulenes, labdanes and a furocurcumene from Ixiolaena leptolepis

Juniperus communis

1 reference

Platelet aggregation inhibitors in a Bhutanese medicinal plant, shug chher

Larix laricina

1 reference

The Volatile Twig and Leaf Oil Terpene Compositions of Three Western North American Larches, Larix laricina, Larix occidentalis, and Larix lyallii

Larix lyallii

1 reference

The Volatile Twig and Leaf Oil Terpene Compositions of Three Western North American Larches, Larix laricina, Larix occidentalis, and Larix lyallii

Larix occidentalis

1 reference

The Volatile Twig and Leaf Oil Terpene Compositions of Three Western North American Larches, Larix laricina, Larix occidentalis, and Larix lyallii

Renealmia alpinia

1 reference

On the characterization of some terpenes fromRenealmia alpinia rott. (maas) oleoresin

Rhizophora mangle

1 reference

Volatile Components of Red Mangrove Bark (Rhizophora mangleL.) from Cuba

Salvia candidissima

1 reference

Terpenoids from Salvia candidissima subsp. candidissima

Salvia multicaulis

1 reference

Norditerpenoids and diterpenoids from Salvia multicaulis with antituberculous activity

Salvia sclarea

4 references

Manool from Salvia sclarea

Terpenoids from Salvia sclarea

Constituents of the Essential Oil of Salvia sclarea Growing Wild in Greece

Terpenoids from Salvia sclarea

Salvia verticillata

1 reference

Figure 8: Seed set of Salvia verticillata.

Senecio erubescens

1 reference

Eremophilane derivatives and other constituents from Senecio species

Senecio macrocephalus

1 reference

Eremophilane derivatives and other constituents from Senecio species

Senecio variabilis

1 reference

Further pyrrolizidine alkaloids and furoeremophilanes from Senecio species

Viguiera dentata

1 reference

Terpenoid constituents of Viguiera dentata

Vitex agnus-castus

2 references

Pyrolysis gas chromatography/mass spectrometry used to simultaneously determine essential oil and phenolic compounds in the monks' peppervitex agnus-castus L

Composition of the essential fruit oil of Vitex agnus-castus

Abies spectabilis

1 reference

Systematic phytochemical investigation of Abies spectabilis.

Cedrus atlantica

1 reference

Antibacterial diterpenoids from Cedrus atlantica.

Larix gmelinii var. olgensis

1 reference

Terpenoids of the oleoresin of Larix olgensis

Porodaedalea pini

1 reference

Inhibition of nitric oxide production in RAW 264.7 macrophages by diterpenoids from Phellinus pini

Pinus contorta

1 reference

Diterpene Constituents of Pinus contorta Bark

Solidago rugosa

1 reference

Diterpenes from Solidago rugosa

Salvia majdae

1 reference

Two diterpenes with rearranged abietane skeletons from Zhumeria majdae

Murraya paniculata

1 reference

Identification of chemical constituents and larvicidal activity of essential oil from Murraya exotica L. (Rutaceae) against Aedes aegypti, Anopheles stephensi and Culex quinquefasciatus (Diptera: Culicidae).

Murraya exotica

1 reference

Identification of chemical constituents and larvicidal activity of essential oil from Murraya exotica L. (Rutaceae) against Aedes aegypti, Anopheles stephensi and Culex quinquefasciatus (Diptera: Culicidae).

Cupressus sempervirens

1 reference

Sempervirol, a novel type of diterpene phenol

Glycosmis pentaphylla

1 reference

Identification of chemical constituents and larvicidal activity of essential oil from Murraya exotica L. (Rutaceae) against Aedes aegypti, Anopheles stephensi and Culex quinquefasciatus (Diptera: Culicidae).

Identifiers

InChI

InChI=1S/C20H34O/c1-7-19(5,21)14-11-16-15(2)9-10-17-18(3,4)12-8-13-20(16,17)6/h7,16-17,21H,1-2,8-14H2,3-6H3/t16-,17-,19-,20+/m0/s1

1 reference

Manool (English)

8 October 2016

2 references

imported from Wikimedia project

Manool (English)

8 October 2016

ChEBI release 2020-09-01

CAS Registry Number

596-85-0

3 references

manool (English)

8 October 2016

https://commonchemistry.cas.org/detail?cas_rn=596-85-0

10 April 2021

1 reference

(+)-manool (English)

8 October 2016

2 references

English

Manool (English)

matched by identifier from

8 October 2016

InChIKey

Reaxys registry number

5273610

1 reference

manool (English)

8 October 2016

mapping relation type

2 references

English

manool (English)

matched by identifier from

8 October 2016

International Chemical Identifier

InChI

InChI=1S/C20H34O/c1-7-19(5,21)14-11-16-15(2)9-10-17-18(3,4)12-8-13-20(16,17)6/h7,16-17,21H,1-2,8-14H2,3-6H3/t16-,17-,19-,20+/m0/s1

1 reference

0 references

DSSTOX compound identifier

0 references

0 references

1 reference

ECHA Substance Infocard database

ECHA Substance Infocard ID

100.165.078

27 December 2018

ECHA Substance Infocard ID

(3R)-3-methyl-5-[(1S,4aS,8aS)-5,5,8a-trimethyl-2-methylenedecahydronaphthalen-1-yl]pent-1-en-3-ol (English)

quotation

CAS no.: 596-85-0 (English)

100.165.078

1 reference

ECHA Substance Infocard database

ECHA Substance Infocard ID

100.165.078

27 December 2018

matched by identifier from

(3R)-3-methyl-5-[(1S,4aS,8aS)-5,5,8a-trimethyl-2-methylenedecahydronaphthalen-1-yl]pent-1-en-3-ol (English)

quotation

CAS no.: 596-85-0 (English)

UNII

AT5PJ0PV00

1 reference

InChIKey