(1R,4S,4aR,8aS)-4,7-dimethyl-1-prop-1-en-2-yl-3,4,4a,5,6,8a-hexahydro-2H-naphthalen-1-ol

Details

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Internal ID 60343892-9f44-49c6-9a6c-693986f92d0c
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name (1R,4S,4aR,8aS)-4,7-dimethyl-1-prop-1-en-2-yl-3,4,4a,5,6,8a-hexahydro-2H-naphthalen-1-ol
SMILES (Canonical) CC1CCC(C2C1CCC(=C2)C)(C(=C)C)O
SMILES (Isomeric) C[C@H]1CC[C@@]([C@H]2[C@@H]1CCC(=C2)C)(C(=C)C)O
InChI InChI=1S/C15H24O/c1-10(2)15(16)8-7-12(4)13-6-5-11(3)9-14(13)15/h9,12-14,16H,1,5-8H2,2-4H3/t12-,13+,14+,15-/m0/s1
InChI Key CUVJTROTJRHROZ-YJNKXOJESA-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 3.60
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 (1R,4S,4aR,8aS)-4,7-dimethyl-1-prop-1-en-2-yl-3,4,4a,5,6,8a-hexahydro-2H-naphthalen-1-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9966 99.66%
Caco-2 + 0.8831 88.31%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Lysosomes 0.6062 60.62%
OATP2B1 inhibitior - 0.8477 84.77%
OATP1B1 inhibitior + 0.9501 95.01%
OATP1B3 inhibitior + 0.8782 87.82%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.5500 55.00%
BSEP inhibitior - 0.9417 94.17%
P-glycoprotein inhibitior - 0.9510 95.10%
P-glycoprotein substrate - 0.8535 85.35%
CYP3A4 substrate + 0.5677 56.77%
CYP2C9 substrate - 0.5471 54.71%
CYP2D6 substrate - 0.7267 72.67%
CYP3A4 inhibition - 0.7073 70.73%
CYP2C9 inhibition - 0.6388 63.88%
CYP2C19 inhibition - 0.5712 57.12%
CYP2D6 inhibition - 0.9372 93.72%
CYP1A2 inhibition - 0.7697 76.97%
CYP2C8 inhibition - 0.8564 85.64%
CYP inhibitory promiscuity - 0.8746 87.46%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.8900 89.00%
Carcinogenicity (trinary) Non-required 0.5655 56.55%
Eye corrosion - 0.9777 97.77%
Eye irritation - 0.5554 55.54%
Skin irritation + 0.6266 62.66%
Skin corrosion - 0.9389 93.89%
Ames mutagenesis - 0.8970 89.70%
Human Ether-a-go-go-Related Gene inhibition - 0.4923 49.23%
Micronuclear - 0.9800 98.00%
Hepatotoxicity + 0.7129 71.29%
skin sensitisation + 0.6473 64.73%
Respiratory toxicity + 0.5111 51.11%
Reproductive toxicity + 0.7111 71.11%
Mitochondrial toxicity + 0.7125 71.25%
Nephrotoxicity - 0.7604 76.04%
Acute Oral Toxicity (c) III 0.8681 86.81%
Estrogen receptor binding - 0.8236 82.36%
Androgen receptor binding - 0.5000 50.00%
Thyroid receptor binding - 0.5336 53.36%
Glucocorticoid receptor binding - 0.7109 71.09%
Aromatase binding - 0.6842 68.42%
PPAR gamma - 0.7491 74.91%
Honey bee toxicity - 0.8533 85.33%
Biodegradation - 0.5500 55.00%
Crustacea aquatic toxicity + 0.5200 52.00%
Fish aquatic toxicity + 0.9831 98.31%

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 95.95% 91.11%
CHEMBL253 P34972 Cannabinoid CB2 receptor 94.38% 97.25%
CHEMBL1994 P08235 Mineralocorticoid receptor 88.50% 100.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.35% 96.09%
CHEMBL241 Q14432 Phosphodiesterase 3A 86.86% 92.94%
CHEMBL2581 P07339 Cathepsin D 84.31% 98.95%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 83.31% 86.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 81.08% 95.56%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 80.96% 93.04%
CHEMBL259 P32245 Melanocortin receptor 4 80.05% 95.38%

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.
Marsupella aquatica

Cross-Links

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PubChem 102575400
LOTUS LTS0257484
wikiData Q104970521