(8R,8aS)-3,8-dimethyl-5-propan-2-yl-1,2,6,7,8,8a-hexahydroazulene

Details

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Internal ID ba1780b4-f7a1-4426-80b4-8c159e7723fb
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids > Guaianes
IUPAC Name (8R,8aS)-3,8-dimethyl-5-propan-2-yl-1,2,6,7,8,8a-hexahydroazulene
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H24/c1-10(2)13-7-5-11(3)14-8-6-12(4)15(14)9-13/h9-11,14H,5-8H2,1-4H3/t11-,14+/m1/s1
InChI Key HLXDFKWNOTZIEI-RISCZKNCSA-N
Popularity 2 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 4.00
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 (8R,8aS)-3,8-dimethyl-5-propan-2-yl-1,2,6,7,8,8a-hexahydroazulene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9939 99.39%
Caco-2 + 0.9541 95.41%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability + 0.6714 67.14%
Subcellular localzation Lysosomes 0.5690 56.90%
OATP2B1 inhibitior - 0.8451 84.51%
OATP1B1 inhibitior + 0.9424 94.24%
OATP1B3 inhibitior + 0.9656 96.56%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior - 0.8770 87.70%
P-glycoprotein inhibitior - 0.9025 90.25%
P-glycoprotein substrate - 0.8572 85.72%
CYP3A4 substrate - 0.5507 55.07%
CYP2C9 substrate - 0.8153 81.53%
CYP2D6 substrate - 0.7357 73.57%
CYP3A4 inhibition - 0.9636 96.36%
CYP2C9 inhibition - 0.7633 76.33%
CYP2C19 inhibition - 0.7642 76.42%
CYP2D6 inhibition - 0.9215 92.15%
CYP1A2 inhibition - 0.6394 63.94%
CYP2C8 inhibition - 0.9282 92.82%
CYP inhibitory promiscuity - 0.7706 77.06%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7500 75.00%
Carcinogenicity (trinary) Non-required 0.4614 46.14%
Eye corrosion - 0.8353 83.53%
Eye irritation + 0.6820 68.20%
Skin irritation + 0.5993 59.93%
Skin corrosion - 0.9622 96.22%
Ames mutagenesis - 0.8300 83.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7783 77.83%
Micronuclear - 0.9900 99.00%
Hepatotoxicity + 0.7125 71.25%
skin sensitisation + 0.8446 84.46%
Respiratory toxicity + 0.5778 57.78%
Reproductive toxicity - 0.7111 71.11%
Mitochondrial toxicity - 0.5750 57.50%
Nephrotoxicity - 0.8090 80.90%
Acute Oral Toxicity (c) III 0.8364 83.64%
Estrogen receptor binding - 0.9595 95.95%
Androgen receptor binding - 0.5990 59.90%
Thyroid receptor binding - 0.6889 68.89%
Glucocorticoid receptor binding - 0.8769 87.69%
Aromatase binding - 0.8610 86.10%
PPAR gamma - 0.9021 90.21%
Honey bee toxicity - 0.9543 95.43%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity + 0.7500 75.00%
Fish aquatic toxicity + 0.9959 99.59%

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 88.63% 96.09%
CHEMBL2581 P07339 Cathepsin D 88.43% 98.95%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 86.00% 86.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 84.29% 97.09%
CHEMBL3359 P21462 Formyl peptide receptor 1 84.23% 93.56%
CHEMBL1907594 P30926 Neuronal acetylcholine receptor; alpha3/beta4 83.43% 97.23%
CHEMBL1994 P08235 Mineralocorticoid receptor 82.65% 100.00%
CHEMBL253 P34972 Cannabinoid CB2 receptor 81.69% 97.25%
CHEMBL3155 P34969 Serotonin 7 (5-HT7) receptor 80.88% 90.71%

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.
Bryopteris filicina

Cross-Links

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PubChem 11447054
LOTUS LTS0122705
wikiData Q105030369