3,8-Dimethyl-5-prop-1-en-2-yl-1,2,3,4,4a,5,6,7-octahydronaphthalene

Details

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Internal ID 60e30315-9401-4c79-a43b-0ebf34c73c73
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name 3,8-dimethyl-5-prop-1-en-2-yl-1,2,3,4,4a,5,6,7-octahydronaphthalene
SMILES (Canonical) CC1CCC2=C(CCC(C2C1)C(=C)C)C
SMILES (Isomeric) CC1CCC2=C(CCC(C2C1)C(=C)C)C
InChI InChI=1S/C15H24/c1-10(2)13-8-6-12(4)14-7-5-11(3)9-15(13)14/h11,13,15H,1,5-9H2,2-4H3
InChI Key YYYXNMTVZFIDGU-UHFFFAOYSA-N
Popularity 0 references 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 4.60
Atomic LogP (AlogP) 4.73
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 3,8-Dimethyl-5-prop-1-en-2-yl-1,2,3,4,4a,5,6,7-octahydronaphthalene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9946 99.46%
Caco-2 + 0.9347 93.47%
Blood Brain Barrier + 0.9000 90.00%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Lysosomes 0.6684 66.84%
OATP2B1 inhibitior - 0.8449 84.49%
OATP1B1 inhibitior + 0.9146 91.46%
OATP1B3 inhibitior + 0.9291 92.91%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior - 0.8514 85.14%
P-glycoprotein inhibitior - 0.8635 86.35%
P-glycoprotein substrate - 0.7906 79.06%
CYP3A4 substrate - 0.5186 51.86%
CYP2C9 substrate - 0.7977 79.77%
CYP2D6 substrate - 0.6973 69.73%
CYP3A4 inhibition - 0.8540 85.40%
CYP2C9 inhibition - 0.7106 71.06%
CYP2C19 inhibition - 0.6363 63.63%
CYP2D6 inhibition - 0.9140 91.40%
CYP1A2 inhibition - 0.6490 64.90%
CYP2C8 inhibition - 0.7719 77.19%
CYP inhibitory promiscuity - 0.6021 60.21%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8100 81.00%
Carcinogenicity (trinary) Non-required 0.4280 42.80%
Eye corrosion - 0.8469 84.69%
Eye irritation + 0.9377 93.77%
Skin irritation - 0.5973 59.73%
Skin corrosion - 0.9376 93.76%
Ames mutagenesis - 0.7623 76.23%
Human Ether-a-go-go-Related Gene inhibition - 0.4610 46.10%
Micronuclear - 0.9800 98.00%
Hepatotoxicity + 0.6250 62.50%
skin sensitisation + 0.8204 82.04%
Respiratory toxicity - 0.7444 74.44%
Reproductive toxicity - 0.6556 65.56%
Mitochondrial toxicity - 0.6250 62.50%
Nephrotoxicity - 0.5522 55.22%
Acute Oral Toxicity (c) III 0.8273 82.73%
Estrogen receptor binding - 0.8949 89.49%
Androgen receptor binding + 0.5397 53.97%
Thyroid receptor binding - 0.6053 60.53%
Glucocorticoid receptor binding - 0.7317 73.17%
Aromatase binding - 0.7555 75.55%
PPAR gamma - 0.7712 77.12%
Honey bee toxicity - 0.9297 92.97%
Biodegradation + 0.5500 55.00%
Crustacea aquatic toxicity - 0.5500 55.00%
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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.81% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 85.98% 97.25%
CHEMBL1994 P08235 Mineralocorticoid receptor 84.32% 100.00%
CHEMBL241 Q14432 Phosphodiesterase 3A 83.70% 92.94%
CHEMBL1871 P10275 Androgen Receptor 81.13% 96.43%
CHEMBL3137262 O60341 LSD1/CoREST complex 80.68% 97.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 80.35% 95.56%

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.
Halocarpus biformis
Metrosideros umbellata

Cross-Links

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PubChem 101418053
LOTUS LTS0188755
wikiData Q105369025