Isocaryophyllene

Details

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Internal ID b2578392-0d8a-41fb-ba3b-2be284a4e48b
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name (1R,4Z,9S)-4,11,11-trimethyl-8-methylidenebicyclo[7.2.0]undec-4-ene
SMILES (Canonical) CC1=CCCC(=C)C2CC(C2CC1)(C)C
SMILES (Isomeric) C/C/1=C/CCC(=C)[C@H]2CC([C@@H]2CC1)(C)C
InChI InChI=1S/C15H24/c1-11-6-5-7-12(2)13-10-15(3,4)14(13)9-8-11/h6,13-14H,2,5,7-10H2,1,3-4H3/b11-6-/t13-,14-/m1/s1
InChI Key NPNUFJAVOOONJE-FLFDDASRSA-N
Popularity 787 references in papers

Physical and Chemical Properties

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Molecular Formula C15H24
Molecular Weight 204.35 g/mol
Exact Mass 204.187800766 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 4.40
Atomic LogP (AlogP) 4.73
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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Caryophyllene
118-65-0
(-)-ISOCARYOPHYLLENE
Cis-caryophyllene
gamma-caryophyllene
NRY8I0KNIR
UNII-NRY8I0KNIR
87-44-5
Isocaryophyllene (80per cent)
Caryophyllene (VAN)
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Isocaryophyllene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9881 98.81%
Caco-2 + 0.8656 86.56%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability + 0.6429 64.29%
Subcellular localzation Lysosomes 0.6916 69.16%
OATP2B1 inhibitior - 0.8477 84.77%
OATP1B1 inhibitior + 0.9400 94.00%
OATP1B3 inhibitior + 0.9479 94.79%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior - 0.6859 68.59%
P-glycoprotein inhibitior - 0.8955 89.55%
P-glycoprotein substrate - 0.9354 93.54%
CYP3A4 substrate + 0.5286 52.86%
CYP2C9 substrate - 0.7890 78.90%
CYP2D6 substrate - 0.7441 74.41%
CYP3A4 inhibition - 0.8665 86.65%
CYP2C9 inhibition - 0.6249 62.49%
CYP2C19 inhibition - 0.5957 59.57%
CYP2D6 inhibition - 0.9284 92.84%
CYP1A2 inhibition - 0.6695 66.95%
CYP2C8 inhibition - 0.6185 61.85%
CYP inhibitory promiscuity - 0.8433 84.33%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6500 65.00%
Carcinogenicity (trinary) Warning 0.4768 47.68%
Eye corrosion - 0.8380 83.80%
Eye irritation + 0.7064 70.64%
Skin irritation + 0.6323 63.23%
Skin corrosion - 0.9744 97.44%
Ames mutagenesis - 1.0000 100.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6851 68.51%
Micronuclear - 0.9800 98.00%
Hepatotoxicity - 0.8250 82.50%
skin sensitisation + 0.8238 82.38%
Respiratory toxicity - 0.5556 55.56%
Reproductive toxicity - 0.7889 78.89%
Mitochondrial toxicity - 0.5125 51.25%
Nephrotoxicity + 0.5165 51.65%
Acute Oral Toxicity (c) III 0.8200 82.00%
Estrogen receptor binding - 0.9345 93.45%
Androgen receptor binding - 0.5966 59.66%
Thyroid receptor binding - 0.8462 84.62%
Glucocorticoid receptor binding - 0.6499 64.99%
Aromatase binding - 0.7885 78.85%
PPAR gamma - 0.8349 83.49%
Honey bee toxicity - 0.8948 89.48%
Biodegradation - 0.5250 52.50%
Crustacea aquatic toxicity + 0.7300 73.00%
Fish aquatic toxicity + 0.9973 99.73%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
CHEMBL253 P34972 Cannabinoid CB2 receptor 150 nM
Ki
via Super-PRED

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.52% 91.11%
CHEMBL1994 P08235 Mineralocorticoid receptor 89.49% 100.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 89.15% 97.09%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.16% 96.09%
CHEMBL241 Q14432 Phosphodiesterase 3A 85.53% 92.94%
CHEMBL1871 P10275 Androgen Receptor 85.12% 96.43%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.93% 95.89%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 82.93% 95.56%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 81.96% 93.40%
CHEMBL221 P23219 Cyclooxygenase-1 80.36% 90.17%

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.
Agastache rugosa
Agrimonia pilosa
Aloysia citrodora
Aloysia gratissima
Angelica archangelica
Artemisia annua
Artemisia argyi
Artemisia capillaris
Artemisia carvifolia
Artemisia filifolia
Artemisia montana
Artemisia princeps
Asarum asperum
Atractylodes lancea
Aucklandia costus
Azadirachta indica
Baccharis coridifolia
Blepharocalyx salicifolius
Brucea javanica
Cannabis sativa
Cassinia laevis
Chrysanthemum indicum
Cinnamomum aromaticum
Citrus × aurantium
Citrus deliciosa
Citrus medica
Citrus trifoliata
Croton flavens
Cryptomeria japonica
Cuminum cyminum
Curcuma kwangsiensis
Curcuma longa
Curcuma phaeocaulis
Curcuma pierreana
Curcuma wenyujin
Curcuma zedoaria
Dendropanax trifidus
Dolomiaea souliei
Elettaria cardamomum
Elsholtzia ciliata
Erigeron bonariensis
Eugenia uniflora
Ferula fukanensis
Foeniculum vulgare
Houttuynia cordata
Humulus lupulus
Hypericum perforatum
Illicium difengpi
Illicium verum
Laggera crispata
Leonurus japonicus
Litsea cubeba
Magnolia biondii
Magnolia denudata
Magnolia kobus
Magnolia obovata
Magnolia officinalis
Magnolia salicifolia
Magnolia sprengeri
Mentha arvensis
Mentha canadensis
Monosis parishii
Mosla chinensis
Murraya exotica
Murraya paniculata
Myristica fragrans
Ocimum gratissimum
Othonna obtusiloba
Panax ginseng
Panax notoginseng
Panax quinquefolius
Perilla frutescens
Perilla frutescens var. hirtella
Persicaria minor
Piper cubeba
Piper nigrum
Platycladus orientalis
Pogostemon cablin
Sagittaria sagittifolia
Salvia dorisiana
Santolina chamaecyparissus
Satureja cuneifolia
Schisandra chinensis
Scutellaria barbata
Syzygium aromaticum
Tetradenia riparia
Tetradium ruticarpum
Thymus funkii
Thymus quinquecostatus
Thymus vulgaris
Vincetoxicum glaucescens
Vincetoxicum stauntonii
Vismia cayennensis
Vitex negundo
Vitex trifolia
Wurfbainia longiligularis
Wurfbainia villosa
Wurfbainia villosa var. xanthioides
Zanthoxylum bungeanum
Zanthoxylum schinifolium
Zingiber officinale
Ziziphus jujuba

Cross-Links

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PubChem 5281522
NPASS NPC60556
LOTUS LTS0141501
wikiData Q27106968