Caryophyllene, 14-hydroxy-

Details

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Internal ID d37e4332-56e0-491d-9f25-65e2986bf092
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name [(1R,4Z,9S)-11,11-dimethyl-8-methylidene-4-bicyclo[7.2.0]undec-4-enyl]methanol
SMILES (Canonical) CC1(CC2C1CCC(=CCCC2=C)CO)C
SMILES (Isomeric) CC1(C[C@H]2[C@H]1CC/C(=C/CCC2=C)/CO)C
InChI InChI=1S/C15H24O/c1-11-5-4-6-12(10-16)7-8-14-13(11)9-15(14,2)3/h6,13-14,16H,1,4-5,7-10H2,2-3H3/b12-6-/t13-,14-/m1/s1
InChI Key MGIQTXDHQJGPEZ-NGPFNDBQSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C15H24O
Molecular Weight 220.35 g/mol
Exact Mass 220.182715385 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 3.10
Atomic LogP (AlogP) 3.70
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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MGIQTXDHQJGPEZ-NGPFNDBQSA-N

2D Structure

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2D Structure of Caryophyllene, 14-hydroxy-

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9883 98.83%
Caco-2 + 0.8460 84.60%
Blood Brain Barrier + 0.9000 90.00%
Human oral bioavailability + 0.5429 54.29%
Subcellular localzation Lysosomes 0.7952 79.52%
OATP2B1 inhibitior - 0.8463 84.63%
OATP1B1 inhibitior + 0.8908 89.08%
OATP1B3 inhibitior + 0.9232 92.32%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior - 0.8098 80.98%
P-glycoprotein inhibitior - 0.8936 89.36%
P-glycoprotein substrate - 0.8782 87.82%
CYP3A4 substrate + 0.5403 54.03%
CYP2C9 substrate - 0.7664 76.64%
CYP2D6 substrate - 0.7388 73.88%
CYP3A4 inhibition - 0.7118 71.18%
CYP2C9 inhibition - 0.6031 60.31%
CYP2C19 inhibition - 0.6767 67.67%
CYP2D6 inhibition - 0.8975 89.75%
CYP1A2 inhibition - 0.7549 75.49%
CYP2C8 inhibition - 0.6285 62.85%
CYP inhibitory promiscuity - 0.8200 82.00%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.7700 77.00%
Carcinogenicity (trinary) Non-required 0.6091 60.91%
Eye corrosion - 0.8870 88.70%
Eye irritation + 0.5742 57.42%
Skin irritation - 0.6395 63.95%
Skin corrosion - 0.9570 95.70%
Ames mutagenesis - 0.8200 82.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4773 47.73%
Micronuclear - 0.9600 96.00%
Hepatotoxicity - 0.6500 65.00%
skin sensitisation + 0.7686 76.86%
Respiratory toxicity + 0.5111 51.11%
Reproductive toxicity - 0.7778 77.78%
Mitochondrial toxicity + 0.5250 52.50%
Nephrotoxicity - 0.6956 69.56%
Acute Oral Toxicity (c) III 0.6306 63.06%
Estrogen receptor binding - 0.8412 84.12%
Androgen receptor binding - 0.6187 61.87%
Thyroid receptor binding - 0.7868 78.68%
Glucocorticoid receptor binding + 0.6342 63.42%
Aromatase binding - 0.7298 72.98%
PPAR gamma - 0.8071 80.71%
Honey bee toxicity - 0.9169 91.69%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity - 0.5800 58.00%
Fish aquatic toxicity + 0.9884 98.84%

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 98.56% 97.25%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.40% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.35% 96.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 91.63% 100.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 91.24% 97.09%
CHEMBL226 P30542 Adenosine A1 receptor 87.59% 95.93%
CHEMBL5608 Q16288 NT-3 growth factor receptor 83.97% 95.89%
CHEMBL4208 P20618 Proteasome component C5 82.12% 90.00%
CHEMBL4040 P28482 MAP kinase ERK2 81.52% 83.82%

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.
Betula pendula
Pterocaulon serrulatum

Cross-Links

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PubChem 6430534
LOTUS LTS0064086
wikiData Q105163339