Caryophylla-2(12),6-dien-5-one

Details

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Internal ID 843375ae-b56c-4775-9e09-67cdaaebf9ad
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name (1R,3Z,9S)-4,11,11-trimethyl-8-methylidenebicyclo[7.2.0]undec-3-en-5-one
SMILES (Canonical) CC1=CCC2C(CC2(C)C)C(=C)CCC1=O
SMILES (Isomeric) C/C/1=C/C[C@@H]2[C@H](CC2(C)C)C(=C)CCC1=O
InChI InChI=1S/C15H22O/c1-10-6-8-14(16)11(2)5-7-13-12(10)9-15(13,3)4/h5,12-13H,1,6-9H2,2-4H3/b11-5-/t12-,13-/m1/s1
InChI Key UVPVOJNEDSOAHT-WNIKWDQDSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H22O
Molecular Weight 218.33 g/mol
Exact Mass 218.167065321 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 3.50
Atomic LogP (AlogP) 3.90
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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caryophylla-2(12),6-dien-5-one

2D Structure

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2D Structure of Caryophylla-2(12),6-dien-5-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9946 99.46%
Caco-2 + 0.8912 89.12%
Blood Brain Barrier + 0.7500 75.00%
Human oral bioavailability + 0.6571 65.71%
Subcellular localzation Mitochondria 0.4273 42.73%
OATP2B1 inhibitior - 0.8498 84.98%
OATP1B1 inhibitior + 0.8354 83.54%
OATP1B3 inhibitior - 0.5698 56.98%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior - 0.7803 78.03%
P-glycoprotein inhibitior - 0.9255 92.55%
P-glycoprotein substrate - 0.9188 91.88%
CYP3A4 substrate + 0.5653 56.53%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8716 87.16%
CYP3A4 inhibition - 0.8309 83.09%
CYP2C9 inhibition - 0.7748 77.48%
CYP2C19 inhibition - 0.6445 64.45%
CYP2D6 inhibition - 0.9476 94.76%
CYP1A2 inhibition - 0.5876 58.76%
CYP2C8 inhibition - 0.8860 88.60%
CYP inhibitory promiscuity - 0.9217 92.17%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8400 84.00%
Carcinogenicity (trinary) Non-required 0.4991 49.91%
Eye corrosion - 0.9380 93.80%
Eye irritation + 0.8514 85.14%
Skin irritation + 0.6940 69.40%
Skin corrosion - 0.9666 96.66%
Ames mutagenesis - 0.7800 78.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3664 36.64%
Micronuclear - 0.9600 96.00%
Hepatotoxicity + 0.5250 52.50%
skin sensitisation + 0.8360 83.60%
Respiratory toxicity + 0.5222 52.22%
Reproductive toxicity - 0.6111 61.11%
Mitochondrial toxicity - 0.6625 66.25%
Nephrotoxicity + 0.6572 65.72%
Acute Oral Toxicity (c) III 0.6806 68.06%
Estrogen receptor binding - 0.9397 93.97%
Androgen receptor binding - 0.6034 60.34%
Thyroid receptor binding - 0.7105 71.05%
Glucocorticoid receptor binding - 0.6813 68.13%
Aromatase binding - 0.7518 75.18%
PPAR gamma - 0.7583 75.83%
Honey bee toxicity - 0.8225 82.25%
Biodegradation + 0.5250 52.50%
Crustacea aquatic toxicity + 0.6100 61.00%
Fish aquatic toxicity + 0.9842 98.42%

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 94.31% 97.25%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.95% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.80% 95.56%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 90.58% 93.40%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.88% 96.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 85.63% 100.00%
CHEMBL1937 Q92769 Histone deacetylase 2 84.80% 94.75%
CHEMBL2581 P07339 Cathepsin D 84.28% 98.95%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 83.04% 90.71%
CHEMBL1871 P10275 Androgen Receptor 81.73% 96.43%
CHEMBL4685 P14902 Indoleamine 2,3-dioxygenase 80.35% 96.38%

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.
Artemisia argyi
Artemisia montana
Artemisia princeps

Cross-Links

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PubChem 91748678
NPASS NPC16182