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

Details

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Internal ID af16f68e-af58-47c9-8724-01a93558d9b2
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name (4R,4aR,6R,8aS)-4,8a-dimethyl-6-prop-1-en-2-yl-2,3,4,4a,5,6-hexahydro-1H-naphthalene
SMILES (Canonical) CC1CCCC2(C1CC(C=C2)C(=C)C)C
SMILES (Isomeric) C[C@@H]1CCC[C@@]2([C@@H]1C[C@H](C=C2)C(=C)C)C
InChI InChI=1S/C15H24/c1-11(2)13-7-9-15(4)8-5-6-12(3)14(15)10-13/h7,9,12-14H,1,5-6,8,10H2,2-4H3/t12-,13+,14-,15+/m1/s1
InChI Key VTGQKWZAEGHONH-BARDWOONSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C15H24
Molecular Weight 204.35 g/mol
Exact Mass 204.187800766 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 5.90
Atomic LogP (AlogP) 4.58
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (4R,4aR,6R,8aS)-4,8a-dimethyl-6-prop-1-en-2-yl-2,3,4,4a,5,6-hexahydro-1H-naphthalene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9926 99.26%
Caco-2 + 0.8304 83.04%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Lysosomes 0.7525 75.25%
OATP2B1 inhibitior - 0.8532 85.32%
OATP1B1 inhibitior + 0.9241 92.41%
OATP1B3 inhibitior + 0.8939 89.39%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.6500 65.00%
BSEP inhibitior - 0.8477 84.77%
P-glycoprotein inhibitior - 0.9490 94.90%
P-glycoprotein substrate - 0.7633 76.33%
CYP3A4 substrate + 0.5803 58.03%
CYP2C9 substrate - 0.7853 78.53%
CYP2D6 substrate - 0.7460 74.60%
CYP3A4 inhibition - 0.7309 73.09%
CYP2C9 inhibition - 0.6961 69.61%
CYP2C19 inhibition - 0.5830 58.30%
CYP2D6 inhibition - 0.9238 92.38%
CYP1A2 inhibition - 0.7962 79.62%
CYP2C8 inhibition - 0.8426 84.26%
CYP inhibitory promiscuity - 0.6408 64.08%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7800 78.00%
Carcinogenicity (trinary) Warning 0.4497 44.97%
Eye corrosion - 0.9143 91.43%
Eye irritation - 0.6975 69.75%
Skin irritation - 0.5915 59.15%
Skin corrosion - 0.9580 95.80%
Ames mutagenesis - 0.7970 79.70%
Human Ether-a-go-go-Related Gene inhibition + 0.6411 64.11%
Micronuclear - 0.9800 98.00%
Hepatotoxicity + 0.6176 61.76%
skin sensitisation + 0.8210 82.10%
Respiratory toxicity - 0.5333 53.33%
Reproductive toxicity - 0.6111 61.11%
Mitochondrial toxicity - 0.5625 56.25%
Nephrotoxicity - 0.6952 69.52%
Acute Oral Toxicity (c) III 0.8468 84.68%
Estrogen receptor binding - 0.8679 86.79%
Androgen receptor binding - 0.5935 59.35%
Thyroid receptor binding - 0.7197 71.97%
Glucocorticoid receptor binding - 0.7186 71.86%
Aromatase binding - 0.7880 78.80%
PPAR gamma - 0.8553 85.53%
Honey bee toxicity - 0.8018 80.18%
Biodegradation - 0.5750 57.50%
Crustacea aquatic toxicity + 0.5700 57.00%
Fish aquatic toxicity + 1.0000 100.00%

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 96.89% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.06% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.76% 91.11%
CHEMBL4040 P28482 MAP kinase ERK2 93.23% 83.82%
CHEMBL1951 P21397 Monoamine oxidase A 91.93% 91.49%
CHEMBL3137262 O60341 LSD1/CoREST complex 87.43% 97.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 87.36% 85.14%
CHEMBL1994 P08235 Mineralocorticoid receptor 85.69% 100.00%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 81.65% 93.04%
CHEMBL241 Q14432 Phosphodiesterase 3A 81.20% 92.94%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 80.14% 95.50%

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.
Frullania tamarisci

Cross-Links

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PubChem 163008815
LOTUS LTS0221061
wikiData Q105292721