(1R,4aS,8aS)-8a-deuterio-7-methyl-4-methylidene-1-propan-2-yl-1,2,3,4a,5,6-hexahydronaphthalene

Details

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Internal ID 067e8bcd-fbf5-492f-9dda-238b46ecc7fe
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name (1R,4aS,8aS)-8a-deuterio-7-methyl-4-methylidene-1-propan-2-yl-1,2,3,4a,5,6-hexahydronaphthalene
SMILES (Canonical) CC1=CC2C(CC1)C(=C)CCC2C(C)C
SMILES (Isomeric) [2H][C@]12C=C(CC[C@@H]1C(=C)CC[C@@H]2C(C)C)C
InChI InChI=1S/C15H24/c1-10(2)13-8-6-12(4)14-7-5-11(3)9-15(13)14/h9-10,13-15H,4-8H2,1-3H3/t13-,14-,15-/m1/s1/i15D
InChI Key WRHGORWNJGOVQY-UHTQFYIKSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H24
Molecular Weight 205.36 g/mol
Exact Mass 205.194077511 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 4.30
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 (1R,4aS,8aS)-8a-deuterio-7-methyl-4-methylidene-1-propan-2-yl-1,2,3,4a,5,6-hexahydronaphthalene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9929 99.29%
Caco-2 + 0.8139 81.39%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability + 0.6000 60.00%
Subcellular localzation Lysosomes 0.6999 69.99%
OATP2B1 inhibitior - 0.8523 85.23%
OATP1B1 inhibitior + 0.9242 92.42%
OATP1B3 inhibitior - 0.2680 26.80%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior - 0.8923 89.23%
P-glycoprotein inhibitior - 0.9006 90.06%
P-glycoprotein substrate - 0.8534 85.34%
CYP3A4 substrate - 0.5251 52.51%
CYP2C9 substrate - 0.7977 79.77%
CYP2D6 substrate - 0.6973 69.73%
CYP3A4 inhibition - 0.8073 80.73%
CYP2C9 inhibition - 0.7418 74.18%
CYP2C19 inhibition - 0.5775 57.75%
CYP2D6 inhibition - 0.9388 93.88%
CYP1A2 inhibition - 0.8143 81.43%
CYP2C8 inhibition - 0.9403 94.03%
CYP inhibitory promiscuity - 0.5501 55.01%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7600 76.00%
Carcinogenicity (trinary) Non-required 0.4936 49.36%
Eye corrosion - 0.9530 95.30%
Eye irritation + 0.5635 56.35%
Skin irritation - 0.6483 64.83%
Skin corrosion - 0.9683 96.83%
Ames mutagenesis - 0.7700 77.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7379 73.79%
Micronuclear - 0.9800 98.00%
Hepatotoxicity + 0.6500 65.00%
skin sensitisation + 0.8385 83.85%
Respiratory toxicity - 0.5778 57.78%
Reproductive toxicity - 0.5556 55.56%
Mitochondrial toxicity - 0.6125 61.25%
Nephrotoxicity - 0.5846 58.46%
Acute Oral Toxicity (c) III 0.7647 76.47%
Estrogen receptor binding - 0.8755 87.55%
Androgen receptor binding + 0.5788 57.88%
Thyroid receptor binding - 0.5989 59.89%
Glucocorticoid receptor binding - 0.5952 59.52%
Aromatase binding - 0.8158 81.58%
PPAR gamma - 0.7182 71.82%
Honey bee toxicity - 0.8792 87.92%
Biodegradation + 0.6000 60.00%
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 87.28% 97.25%
CHEMBL3137262 O60341 LSD1/CoREST complex 86.78% 97.09%
CHEMBL1907594 P30926 Neuronal acetylcholine receptor; alpha3/beta4 84.84% 97.23%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.49% 95.56%
CHEMBL2581 P07339 Cathepsin D 83.43% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 82.72% 91.11%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.47% 95.89%
CHEMBL1994 P08235 Mineralocorticoid receptor 82.32% 100.00%
CHEMBL2996 Q05655 Protein kinase C delta 82.17% 97.79%
CHEMBL1871 P10275 Androgen Receptor 81.83% 96.43%
CHEMBL3359 P21462 Formyl peptide receptor 1 80.76% 93.56%

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.
Artemisia annua

Cross-Links

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PubChem 10512446
NPASS NPC49471