Compounds > abieta-7(8),13(14)-diene
Page last updated: 2024-11-08

abieta-7(8),13(14)-diene

Description Research Excerpts Clinical Trials Roles Classes Pathways Study Profile Bioassays Related Drugs Related Conditions Protein Interactions Research Growth Market Indicators

Description

abieta-7(8),13(14)-diene: structure in first source [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

abietadiene : A diterpene consisting of abietane having two C=C double bonds at unspecified positions. [Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Cross-References

ID SourceID
PubMed CID443470
CHEBI ID30232
MeSH IDM0266667

Synonyms (17)

Synonym
CHEBI:30232
phenanthrene, 1,2,3,4,4a,4b,5,6,10,10a-decahydro-1,1,4a-trimethyl-7-(1-methylethyl)-, (4as,4br,10as)-
inchi=1/c20h32/c1-14(2)15-7-9-17-16(13-15)8-10-18-19(3,4)11-6-12-20(17,18)5/h8,13-14,17-18h,6-7,9-12h2,1-5h3/t17-,18-,20+/m0/s
abieta-7,13-diene
35241-40-8
(4as,4br,10as)-7-isopropyl-1,1,4a-trimethyl-1,2,3,4,4a,4b,5,6,10,10a-decahydrophenanthrene
abietadiene
(-)-abietadiene
abieta-7(8),13(14)-diene
7-isopropyl-1,1,4a-trimethyl-1,2,3,4,4a,4b,5,6,10,10a-decahydrophenanthrene
LMPR0104050002
(4as,4br,10as)-1,1,4a-trimethyl-7-propan-2-yl-2,3,4,4b,5,6,10,10a-octahydrophenanthrene
syn-abeita-7,13-diene
smr002134486
MLS003468551
DTXSID40332099
Q27104115
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Drug Classes (1)

ClassDescription
abietadieneA diterpene consisting of abietane having two C=C double bonds at unspecified positions.
[compound class information is derived from Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Pathways (3)

PathwayProteinsCompounds
dehydroabietic acid biosynthesis512
abietic acid biosynthesis513
superpathway of diterpene resin acids biosynthesis523
abietic acid biosynthesis416
superpathway of diterpene resin acids biosynthesis443
dehydroabietic acid biosynthesis414

Research

Studies (5)

TimeframeStudies, This Drug (%)All Drugs %
pre-19900 (0.00)18.7374
1990's1 (20.00)18.2507
2000's2 (40.00)29.6817
2010's2 (40.00)24.3611
2020's0 (0.00)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 12.87

According to the monthly volume, diversity, and competition of internet searches for this compound, as well the volume and growth of publications, there is estimated to be weak demand-to-supply ratio for research on this compound.

MetricThis Compound (vs All)
Research Demand Index12.87 (24.57)
Research Supply Index1.79 (2.92)
Research Growth Index4.66 (4.65)
Search Engine Demand Index0.00 (26.88)
Search Engine Supply Index0.00 (0.95)

This Compound (12.87)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews0 (0.00%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other5 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]
SubstanceRelationship StrengthStudiesTrialsClassesRoles
abietic acid
abietic acid : An abietane diterpenoid that is abieta-7,13-diene substituted by a carboxy group at position 18.		2.7130abietane diterpenoid;
monocarboxylic acid		plant metabolite
totarol
totarol: structure given in first source; isolated from the bark of Podocarpus nagi		2.0410diterpenoidmetabolite
ferruginol
ferruginol: structure in first source. ferruginol : An abietane diterpenoid that is abieta-8,11,13-triene substituted by a hydroxy group at positions 12.		2.0410abietane diterpenoid;
carbotricyclic compound;
meroterpenoid;
phenols		antibacterial agent;
antineoplastic agent;
plant metabolite;
protective agent
geranylgeranyl pyrophosphate
geranylgeranyl pyrophosphate: RN given refers to (E,E,E)-isomer. geranylgeranyl diphosphate : A polyprenol diphosphate having geranylgeranyl as the polyprenyl component.. 2-trans,6-trans,10-trans-geranylgeranyl diphosphate : The all-trans-isomer of geranylgeranyl diphosphate.		1.9910geranylgeranyl diphosphatemouse metabolite
communic acid
communic acid: structure in first source		2.0410
rosin
rosin: Resin from plant. Do not confuse with the specific compound: 3-phenyl-2-propenyl-(E)-beta-D-glucopyranoside, also know as rosin.		2.0610
copalyl diphosphate
copalyl diphosphate: structure in first source. 5alpha,9alpha,10beta-labda-8(20),13-dien-15-yl diphosphate : The 5alpha,9alpha,10beta-diastereomer of copalyl diphosphate.		2.4320copalyl diphosphate
pimarane
pimarane: from Croton joufra; structure in first source		2.0410diterpene;
terpenoid fundamental parent
phenanthrenes
Phenanthrenes: POLYCYCLIC AROMATIC HYDROCARBONS composed of three fused BENZENE rings.. phenanthrenes : Any benzenoid aromatic compound that consists of a phenanthrene skeleton and its substituted derivatives thereof.		2.420
ConditionIndicatedRelationship StrengthStudiesTrials