14-Oxy-alpha-muurolene

Details

Top
Internal ID ce1e6d75-230e-4f69-992d-c0a6184785e7
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name 6-methyl-4-propan-2-yl-3,4,4a,7,8,8a-hexahydronaphthalene-1-carbaldehyde
SMILES (Canonical) CC1=CC2C(CC1)C(=CCC2C(C)C)C=O
SMILES (Isomeric) CC1=CC2C(CC1)C(=CCC2C(C)C)C=O
InChI InChI=1S/C15H22O/c1-10(2)13-7-5-12(9-16)14-6-4-11(3)8-15(13)14/h5,8-10,13-15H,4,6-7H2,1-3H3
InChI Key DNHAZRYDTSOZHV-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C15H22O
Molecular Weight 218.33 g/mol
Exact Mass 218.167065321 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 3.30
Atomic LogP (AlogP) 3.76
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

Top
4,9-Muuroladien-14-al
DNHAZRYDTSOZHV-UHFFFAOYSA-N

2D Structure

Top
2D Structure of 14-Oxy-alpha-muurolene

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 + 0.8555 85.55%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability + 0.6143 61.43%
Subcellular localzation Lysosomes 0.4155 41.55%
OATP2B1 inhibitior - 0.8575 85.75%
OATP1B1 inhibitior + 0.9068 90.68%
OATP1B3 inhibitior + 0.9050 90.50%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior - 0.8447 84.47%
P-glycoprotein inhibitior - 0.9106 91.06%
P-glycoprotein substrate - 0.8862 88.62%
CYP3A4 substrate - 0.5231 52.31%
CYP2C9 substrate - 0.8062 80.62%
CYP2D6 substrate - 0.8279 82.79%
CYP3A4 inhibition - 0.9277 92.77%
CYP2C9 inhibition - 0.8499 84.99%
CYP2C19 inhibition - 0.6331 63.31%
CYP2D6 inhibition - 0.8981 89.81%
CYP1A2 inhibition - 0.7096 70.96%
CYP2C8 inhibition - 0.9209 92.09%
CYP inhibitory promiscuity - 0.5727 57.27%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7700 77.00%
Carcinogenicity (trinary) Non-required 0.5873 58.73%
Eye corrosion - 0.8459 84.59%
Eye irritation - 0.6872 68.72%
Skin irritation + 0.4921 49.21%
Skin corrosion - 0.8904 89.04%
Ames mutagenesis - 0.8400 84.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3986 39.86%
Micronuclear - 0.9626 96.26%
Hepatotoxicity + 0.5375 53.75%
skin sensitisation + 0.9182 91.82%
Respiratory toxicity - 0.6444 64.44%
Reproductive toxicity + 0.6000 60.00%
Mitochondrial toxicity - 0.6750 67.50%
Nephrotoxicity + 0.6651 66.51%
Acute Oral Toxicity (c) III 0.7826 78.26%
Estrogen receptor binding - 0.8642 86.42%
Androgen receptor binding - 0.5333 53.33%
Thyroid receptor binding - 0.7110 71.10%
Glucocorticoid receptor binding - 0.6839 68.39%
Aromatase binding - 0.8247 82.47%
PPAR gamma - 0.7974 79.74%
Honey bee toxicity - 0.8854 88.54%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity + 0.5300 53.00%
Fish aquatic toxicity + 0.9912 99.12%

Targets

Top

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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.86% 95.56%
CHEMBL2581 P07339 Cathepsin D 90.11% 98.95%
CHEMBL253 P34972 Cannabinoid CB2 receptor 87.18% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.89% 96.09%
CHEMBL3359 P21462 Formyl peptide receptor 1 84.26% 93.56%
CHEMBL1994 P08235 Mineralocorticoid receptor 83.52% 100.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 83.23% 91.11%
CHEMBL3137262 O60341 LSD1/CoREST complex 83.01% 97.09%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 80.93% 95.89%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.38% 95.89%

Plants that contains it

Top
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.
Hypericum perforatum
Lindera aggregata

Cross-Links

Top
PubChem 91746681
NPASS NPC90889
LOTUS LTS0230291
wikiData Q104985552