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

Details

Top
Internal ID 168cf306-c97c-446d-8818-6c50abb838c7
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name (1R,4aS,5R,8aS)-3-methyl-8-methylidene-5-propan-2-yl-2,4a,5,6,7,8a-hexahydro-1H-naphthalen-1-ol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H24O/c1-9(2)12-6-5-11(4)15-13(12)7-10(3)8-14(15)16/h7,9,12-16H,4-6,8H2,1-3H3/t12-,13-,14-,15-/m1/s1
InChI Key WFHKESPONQXPGD-KBUPBQIOSA-N
Popularity 3 references in papers

Physical and Chemical Properties

Top
Molecular Formula C15H24O
Molecular Weight 220.35 g/mol
Exact Mass 220.182715385 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 3.20
Atomic LogP (AlogP) 3.55
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

Top
There are no found synonyms.

2D Structure

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

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9963 99.63%
Caco-2 + 0.8271 82.71%
Blood Brain Barrier + 0.5500 55.00%
Human oral bioavailability + 0.6571 65.71%
Subcellular localzation Lysosomes 0.5608 56.08%
OATP2B1 inhibitior - 0.8546 85.46%
OATP1B1 inhibitior + 0.9039 90.39%
OATP1B3 inhibitior + 0.9057 90.57%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior - 0.9353 93.53%
P-glycoprotein inhibitior - 0.9297 92.97%
P-glycoprotein substrate - 0.7760 77.60%
CYP3A4 substrate - 0.5442 54.42%
CYP2C9 substrate - 0.6284 62.84%
CYP2D6 substrate + 0.3479 34.79%
CYP3A4 inhibition - 0.8402 84.02%
CYP2C9 inhibition - 0.8161 81.61%
CYP2C19 inhibition - 0.6953 69.53%
CYP2D6 inhibition - 0.9051 90.51%
CYP1A2 inhibition - 0.6921 69.21%
CYP2C8 inhibition - 0.9515 95.15%
CYP inhibitory promiscuity - 0.8126 81.26%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.8800 88.00%
Carcinogenicity (trinary) Non-required 0.6409 64.09%
Eye corrosion - 0.9575 95.75%
Eye irritation - 0.5176 51.76%
Skin irritation + 0.6069 60.69%
Skin corrosion - 0.8949 89.49%
Ames mutagenesis - 0.7400 74.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4482 44.82%
Micronuclear - 0.9800 98.00%
Hepatotoxicity - 0.5726 57.26%
skin sensitisation + 0.7597 75.97%
Respiratory toxicity - 0.5222 52.22%
Reproductive toxicity + 0.6667 66.67%
Mitochondrial toxicity + 0.6000 60.00%
Nephrotoxicity - 0.5712 57.12%
Acute Oral Toxicity (c) III 0.8147 81.47%
Estrogen receptor binding - 0.8415 84.15%
Androgen receptor binding - 0.5534 55.34%
Thyroid receptor binding - 0.5967 59.67%
Glucocorticoid receptor binding - 0.6631 66.31%
Aromatase binding - 0.8509 85.09%
PPAR gamma - 0.8330 83.30%
Honey bee toxicity - 0.8851 88.51%
Biodegradation - 0.5750 57.50%
Crustacea aquatic toxicity - 0.5400 54.00%
Fish aquatic toxicity + 0.9658 96.58%

Targets

Top

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
CHEMBL2581 P07339 Cathepsin D 88.73% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.67% 96.09%
CHEMBL5608 Q16288 NT-3 growth factor receptor 87.15% 95.89%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 86.58% 91.11%
CHEMBL1871 P10275 Androgen Receptor 85.83% 96.43%
CHEMBL1994 P08235 Mineralocorticoid receptor 84.63% 100.00%
CHEMBL3359 P21462 Formyl peptide receptor 1 83.91% 93.56%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.21% 95.56%
CHEMBL1977 P11473 Vitamin D receptor 82.89% 99.43%
CHEMBL3137262 O60341 LSD1/CoREST complex 81.84% 97.09%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 81.08% 95.89%

Plants that contains it

Top
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.
Cussonia bancoensis

Cross-Links

Top
PubChem 13874489
NPASS NPC21837