5-(3-Hydroxyprop-1-en-2-yl)-3,8-dimethylidene-1,2,3a,4,5,6,7,8a-octahydroazulen-4-ol

Details

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Internal ID 8d414d43-3ecc-4571-bf3d-48bd9e53a13d
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids > Guaianes
IUPAC Name 5-(3-hydroxyprop-1-en-2-yl)-3,8-dimethylidene-1,2,3a,4,5,6,7,8a-octahydroazulen-4-ol
SMILES (Canonical) C=C1CCC(C(C2C1CCC2=C)O)C(=C)CO
SMILES (Isomeric) C=C1CCC(C(C2C1CCC2=C)O)C(=C)CO
InChI InChI=1S/C15H22O2/c1-9-4-7-13(11(3)8-16)15(17)14-10(2)5-6-12(9)14/h12-17H,1-8H2
InChI Key WKISBWAEMCVJQO-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H22O2
Molecular Weight 234.33 g/mol
Exact Mass 234.161979940 g/mol
Topological Polar Surface Area (TPSA) 40.50 Ų
XlogP 1.90
Atomic LogP (AlogP) 2.44
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 5-(3-Hydroxyprop-1-en-2-yl)-3,8-dimethylidene-1,2,3a,4,5,6,7,8a-octahydroazulen-4-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9882 98.82%
Caco-2 - 0.7525 75.25%
Blood Brain Barrier + 0.5500 55.00%
Human oral bioavailability - 0.6429 64.29%
Subcellular localzation Mitochondria 0.4677 46.77%
OATP2B1 inhibitior - 0.8531 85.31%
OATP1B1 inhibitior + 0.9284 92.84%
OATP1B3 inhibitior + 0.9541 95.41%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.7570 75.70%
BSEP inhibitior - 0.9070 90.70%
P-glycoprotein inhibitior - 0.9185 91.85%
P-glycoprotein substrate - 0.8729 87.29%
CYP3A4 substrate - 0.5550 55.50%
CYP2C9 substrate - 0.8066 80.66%
CYP2D6 substrate + 0.3503 35.03%
CYP3A4 inhibition - 0.8791 87.91%
CYP2C9 inhibition - 0.7314 73.14%
CYP2C19 inhibition - 0.7122 71.22%
CYP2D6 inhibition - 0.8186 81.86%
CYP1A2 inhibition - 0.5000 50.00%
CYP2C8 inhibition - 0.8426 84.26%
CYP inhibitory promiscuity - 0.6661 66.61%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.8600 86.00%
Carcinogenicity (trinary) Non-required 0.6503 65.03%
Eye corrosion - 0.9038 90.38%
Eye irritation + 0.7629 76.29%
Skin irritation - 0.7203 72.03%
Skin corrosion - 0.9317 93.17%
Ames mutagenesis - 0.8000 80.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6361 63.61%
Micronuclear - 0.9100 91.00%
Hepatotoxicity - 0.6125 61.25%
skin sensitisation - 0.5515 55.15%
Respiratory toxicity - 0.6778 67.78%
Reproductive toxicity + 0.5222 52.22%
Mitochondrial toxicity + 0.5875 58.75%
Nephrotoxicity + 0.5100 51.00%
Acute Oral Toxicity (c) III 0.6171 61.71%
Estrogen receptor binding - 0.7343 73.43%
Androgen receptor binding - 0.5086 50.86%
Thyroid receptor binding - 0.5811 58.11%
Glucocorticoid receptor binding + 0.5783 57.83%
Aromatase binding - 0.8222 82.22%
PPAR gamma - 0.7817 78.17%
Honey bee toxicity - 0.8462 84.62%
Biodegradation - 0.5000 50.00%
Crustacea aquatic toxicity - 0.6300 63.00%
Fish aquatic toxicity + 0.8741 87.41%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.63% 91.11%
CHEMBL226 P30542 Adenosine A1 receptor 93.54% 95.93%
CHEMBL3137262 O60341 LSD1/CoREST complex 89.01% 97.09%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.94% 96.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 84.87% 100.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.90% 95.89%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 82.77% 95.89%
CHEMBL241 Q14432 Phosphodiesterase 3A 80.14% 92.94%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 85213586
LOTUS LTS0150618
wikiData Q105307366