(3R,4aR,8aS)-8a-methyl-5-methylidene-3-prop-1-en-2-yl-1,2,3,4,4a,8-hexahydronaphthalene

Details

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Internal ID ffec766c-10b7-4a9e-af4a-a86e2bf0dfb2
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name (3R,4aR,8aS)-8a-methyl-5-methylidene-3-prop-1-en-2-yl-1,2,3,4,4a,8-hexahydronaphthalene
SMILES (Canonical) CC(=C)C1CCC2(CC=CC(=C)C2C1)C
SMILES (Isomeric) CC(=C)[C@@H]1CC[C@]2(CC=CC(=C)[C@@H]2C1)C
InChI InChI=1S/C15H22/c1-11(2)13-7-9-15(4)8-5-6-12(3)14(15)10-13/h5-6,13-14H,1,3,7-10H2,2,4H3/t13-,14+,15-/m1/s1
InChI Key DDLAIUOYTHJYGD-QLFBSQMISA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C15H22
Molecular Weight 202.33 g/mol
Exact Mass 202.172150702 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 5.10
Atomic LogP (AlogP) 4.50
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 (3R,4aR,8aS)-8a-methyl-5-methylidene-3-prop-1-en-2-yl-1,2,3,4,4a,8-hexahydronaphthalene

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 + 0.8510 85.10%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Lysosomes 0.7746 77.46%
OATP2B1 inhibitior - 0.8537 85.37%
OATP1B1 inhibitior + 0.9216 92.16%
OATP1B3 inhibitior + 0.9095 90.95%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior - 0.9121 91.21%
P-glycoprotein inhibitior - 0.9689 96.89%
P-glycoprotein substrate - 0.7632 76.32%
CYP3A4 substrate + 0.5700 57.00%
CYP2C9 substrate - 0.6219 62.19%
CYP2D6 substrate - 0.7767 77.67%
CYP3A4 inhibition - 0.7319 73.19%
CYP2C9 inhibition - 0.7746 77.46%
CYP2C19 inhibition - 0.6540 65.40%
CYP2D6 inhibition - 0.9151 91.51%
CYP1A2 inhibition - 0.7761 77.61%
CYP2C8 inhibition - 0.8893 88.93%
CYP inhibitory promiscuity - 0.6460 64.60%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7800 78.00%
Carcinogenicity (trinary) Warning 0.4462 44.62%
Eye corrosion - 0.8931 89.31%
Eye irritation - 0.5448 54.48%
Skin irritation - 0.6352 63.52%
Skin corrosion - 0.9603 96.03%
Ames mutagenesis - 0.8137 81.37%
Human Ether-a-go-go-Related Gene inhibition + 0.6907 69.07%
Micronuclear - 0.9500 95.00%
Hepatotoxicity - 0.5414 54.14%
skin sensitisation + 0.8646 86.46%
Respiratory toxicity + 0.5333 53.33%
Reproductive toxicity - 0.6000 60.00%
Mitochondrial toxicity - 0.5250 52.50%
Nephrotoxicity - 0.6187 61.87%
Acute Oral Toxicity (c) III 0.8388 83.88%
Estrogen receptor binding - 0.8465 84.65%
Androgen receptor binding - 0.6634 66.34%
Thyroid receptor binding - 0.7193 71.93%
Glucocorticoid receptor binding - 0.6898 68.98%
Aromatase binding - 0.7014 70.14%
PPAR gamma - 0.7329 73.29%
Honey bee toxicity - 0.8443 84.43%
Biodegradation + 0.6000 60.00%
Crustacea aquatic toxicity - 0.5300 53.00%
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 96.23% 97.25%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.56% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.13% 96.09%
CHEMBL2996 Q05655 Protein kinase C delta 89.18% 97.79%
CHEMBL3137262 O60341 LSD1/CoREST complex 88.97% 97.09%
CHEMBL4040 P28482 MAP kinase ERK2 87.49% 83.82%
CHEMBL1994 P08235 Mineralocorticoid receptor 85.99% 100.00%
CHEMBL221 P23219 Cyclooxygenase-1 83.04% 90.17%
CHEMBL2581 P07339 Cathepsin D 81.86% 98.95%
CHEMBL4225 P49760 Dual specificity protein kinase CLK2 81.06% 80.96%

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.
Cyperus alopecuroides

Cross-Links

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PubChem 12011811
LOTUS LTS0018555
wikiData Q104976478