2-(7-methyl-4-methylidene-2,3,4a,5,6,8a-hexahydro-1H-naphthalen-1-yl)propan-2-ol

Details

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Internal ID e151b235-f660-41a7-aed4-2f4800d0a5a6
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name 2-(7-methyl-4-methylidene-2,3,4a,5,6,8a-hexahydro-1H-naphthalen-1-yl)propan-2-ol
SMILES (Canonical) CC1=CC2C(CC1)C(=C)CCC2C(C)(C)O
SMILES (Isomeric) CC1=CC2C(CC1)C(=C)CCC2C(C)(C)O
InChI InChI=1S/C15H24O/c1-10-5-7-12-11(2)6-8-14(13(12)9-10)15(3,4)16/h9,12-14,16H,2,5-8H2,1,3-4H3
InChI Key QHNDBEIHGDNMQH-UHFFFAOYSA-N
Popularity 0 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 2.70
Atomic LogP (AlogP) 3.70
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2-(7-methyl-4-methylidene-2,3,4a,5,6,8a-hexahydro-1H-naphthalen-1-yl)propan-2-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9948 99.48%
Caco-2 + 0.7788 77.88%
Blood Brain Barrier + 0.8000 80.00%
Human oral bioavailability + 0.5286 52.86%
Subcellular localzation Lysosomes 0.4945 49.45%
OATP2B1 inhibitior - 0.8477 84.77%
OATP1B1 inhibitior + 0.9146 91.46%
OATP1B3 inhibitior - 0.2642 26.42%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior - 0.9423 94.23%
P-glycoprotein inhibitior - 0.9466 94.66%
P-glycoprotein substrate - 0.8818 88.18%
CYP3A4 substrate - 0.5000 50.00%
CYP2C9 substrate - 0.5471 54.71%
CYP2D6 substrate - 0.7267 72.67%
CYP3A4 inhibition - 0.7681 76.81%
CYP2C9 inhibition + 0.6312 63.12%
CYP2C19 inhibition + 0.6454 64.54%
CYP2D6 inhibition - 0.9193 91.93%
CYP1A2 inhibition - 0.7828 78.28%
CYP2C8 inhibition - 0.7052 70.52%
CYP inhibitory promiscuity - 0.6560 65.60%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.8300 83.00%
Carcinogenicity (trinary) Non-required 0.6147 61.47%
Eye corrosion - 0.9632 96.32%
Eye irritation - 0.6331 63.31%
Skin irritation + 0.5000 50.00%
Skin corrosion - 0.9623 96.23%
Ames mutagenesis - 0.7600 76.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7589 75.89%
Micronuclear - 0.9800 98.00%
Hepatotoxicity + 0.5303 53.03%
skin sensitisation + 0.7946 79.46%
Respiratory toxicity - 0.6889 68.89%
Reproductive toxicity - 0.6333 63.33%
Mitochondrial toxicity + 0.6125 61.25%
Nephrotoxicity - 0.7602 76.02%
Acute Oral Toxicity (c) III 0.6521 65.21%
Estrogen receptor binding - 0.7644 76.44%
Androgen receptor binding - 0.5057 50.57%
Thyroid receptor binding - 0.5862 58.62%
Glucocorticoid receptor binding - 0.6030 60.30%
Aromatase binding - 0.8181 81.81%
PPAR gamma - 0.6940 69.40%
Honey bee toxicity - 0.9394 93.94%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity + 0.5900 59.00%
Fish aquatic toxicity + 0.9970 99.70%

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 95.77% 97.25%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.82% 91.11%
CHEMBL3137262 O60341 LSD1/CoREST complex 86.05% 97.09%
CHEMBL241 Q14432 Phosphodiesterase 3A 83.92% 92.94%
CHEMBL2581 P07339 Cathepsin D 83.05% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 82.78% 95.56%
CHEMBL1977 P11473 Vitamin D receptor 81.70% 99.43%
CHEMBL1994 P08235 Mineralocorticoid receptor 81.58% 100.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.56% 95.89%
CHEMBL5966 P55899 IgG receptor FcRn large subunit p51 81.09% 90.93%
CHEMBL1871 P10275 Androgen Receptor 81.06% 96.43%
CHEMBL5805 Q9NR97 Toll-like receptor 8 80.52% 96.25%

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.
Commiphora kataf

Cross-Links

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PubChem 163075015
LOTUS LTS0224945
wikiData Q105221035