Tricyclene

Details

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Internal ID f04f48a2-04af-45b9-bcf0-03a142396ee4
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids > Bicyclic monoterpenoids
IUPAC Name 1,7,7-trimethyltricyclo[2.2.1.02,6]heptane
SMILES (Canonical) CC1(C2CC3C1(C3C2)C)C
SMILES (Isomeric) CC1(C2CC3C1(C3C2)C)C
InChI InChI=1S/C10H16/c1-9(2)6-4-7-8(5-6)10(7,9)3/h6-8H,4-5H2,1-3H3
InChI Key RRBYUSWBLVXTQN-UHFFFAOYSA-N
Popularity 445 references in papers

Physical and Chemical Properties

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Molecular Formula C10H16
Molecular Weight 136.23 g/mol
Exact Mass 136.125200510 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 3.20

Synonyms

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508-32-7
cyclene
1,7,7-Trimethyltricyclo[2.2.1.02,6]heptane
Tricyclene (VAN)
SA0ARA1GHB
NSC 86978
1,7,7-Trimethyltricyclo(2.2.1.02,6)heptane
1,1,7-Trimethyltricyclo(2.2.1.0(2.6))heptane
EINECS 208-083-7
1,7,7-Trimethyltricyclo(2.2.1.0(sup2,6))heptane
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Tricyclene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
No predicted properties yet!

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
No proven targets yet!

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL253 P34972 Cannabinoid CB2 receptor 90.12% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.60% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 85.32% 97.09%
CHEMBL2996 Q05655 Protein kinase C delta 83.76% 97.79%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
Abies balsamea
Abies sachalinensis
Achillea grandifolia
Achillea millefolium
Acorus calamus
Ageratum conyzoides
Angelica acutiloba
Angelica gigas
Angelica sinensis
Aristolochia debilis
Artemisia annua
Artemisia arborescens
Artemisia argyi
Artemisia capillaris
Artemisia judaica
Artemisia montana
Artemisia princeps
Artemisia salsoloides
Artemisia sericea
Artemisia thuscula
Atalantia buxifolia
Boronia latipinna
Capsicum annuum
Chaerophyllum macrospermum
Chamaecyparis lawsoniana
Chamaecyparis pisifera
Chrysanthemum indicum
Cistus monspeliensis
Cryptomeria japonica
Curcuma kwangsiensis
Curcuma longa
Curcuma phaeocaulis
Curcuma wenyujin
Curcuma zedoaria
Cymbopogon flexuosus
Daucus carota
Hansenia forbesii
Hansenia weberbaueriana
Haplopappus foliosus
Helichrysum odoratissimum
Helichrysum taenari
Hyptis suaveolens
Juniperus monticola
Larix sibirica
Lavandula angustifolia
Magnolia liliiflora
Myrtus communis
Origanum acutidens
Origanum hypericifolium
Origanum minutiflorum
Origanum sipyleum
Origanum syriacum
Pelargonium vitifolium
Persea americana
Picea abies
Picea mariana
Pilocarpus jaborandi
Pinus flexilis
Pinus longaeva
Pinus sylvestris
Piper arboreum
Pistacia vera
Plectranthus ovatus
Pseudotsuga menziesii
Rhododendron mucronulatum
Saccogyna viticulosa
Salvia absconditiflora
Salvia caespitosa
Salvia fruticosa
Salvia syriaca
Scalesia aspera
Schisandra chinensis
Sequoia sempervirens
Seriphidium herba-alba
Sideritis lyciae
Tanacetum annuum
Tanacetum parthenium
Tanacetum vulgare
Thuja occidentalis
Thymus eigii
Thymus funkii
Thymus kotschyanus
Thymus longicaulis
Thymus revolutus
Thymus riatarum
Thymus saturejoides
Thymus thracicus
Thymus willkommii
Thymus zygioides
Tsuga canadensis
Valeriana officinalis
Varronia curassavica
Xylopia sericea
Zanthoxylum bungeanum
Zanthoxylum schinifolium
Zea mays
Zingiber officinale
Zingiber zerumbet

Cross-Links

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PubChem 79035
NPASS NPC135238
LOTUS LTS0179930
wikiData Q27133173