p-Mentha-1,3,8-triene

Details

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Internal ID a1948966-1999-480d-ae10-17621ddb4a8b
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids > Menthane monoterpenoids
IUPAC Name 1-methyl-4-prop-1-en-2-ylcyclohexa-1,3-diene
SMILES (Canonical) CC1=CC=C(CC1)C(=C)C
SMILES (Isomeric) CC1=CC=C(CC1)C(=C)C
InChI InChI=1S/C10H14/c1-8(2)10-6-4-9(3)5-7-10/h4,6H,1,5,7H2,2-3H3
InChI Key XNMPFDIYAMOYRM-UHFFFAOYSA-N
Popularity 80 references in papers

Physical and Chemical Properties

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Molecular Formula C10H14
Molecular Weight 134.22 g/mol
Exact Mass 134.109550447 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 3.00
Atomic LogP (AlogP) 3.23
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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1,3,8-p-Menthatriene
p-Menthatriene
18368-95-1
1-methyl-4-prop-1-en-2-ylcyclohexa-1,3-diene
p-1,3,8-Menthatriene
p-Menta-1,3,8-triene
1,3,8-para-Menthatriene
1,3,8-menthatriene
1,3-Cyclohexadiene, 1-methyl-4-(1-methylethenyl)-
ZDY5H4QWH3
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of p-Mentha-1,3,8-triene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9905 99.05%
Caco-2 + 0.9578 95.78%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.7000 70.00%
Subcellular localzation Lysosomes 0.6553 65.53%
OATP2B1 inhibitior - 0.8609 86.09%
OATP1B1 inhibitior + 0.9626 96.26%
OATP1B3 inhibitior + 0.9059 90.59%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior - 0.9161 91.61%
P-glycoprotein inhibitior - 0.9831 98.31%
P-glycoprotein substrate - 0.9627 96.27%
CYP3A4 substrate - 0.6711 67.11%
CYP2C9 substrate - 0.8209 82.09%
CYP2D6 substrate - 0.7550 75.50%
CYP3A4 inhibition - 0.9338 93.38%
CYP2C9 inhibition - 0.9428 94.28%
CYP2C19 inhibition - 0.8747 87.47%
CYP2D6 inhibition - 0.9221 92.21%
CYP1A2 inhibition - 0.7624 76.24%
CYP2C8 inhibition - 0.9740 97.40%
CYP inhibitory promiscuity - 0.7657 76.57%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6300 63.00%
Carcinogenicity (trinary) Warning 0.5094 50.94%
Eye corrosion + 0.7819 78.19%
Eye irritation + 0.9827 98.27%
Skin irritation + 0.8430 84.30%
Skin corrosion - 0.9603 96.03%
Ames mutagenesis - 0.8700 87.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5805 58.05%
Micronuclear - 0.9900 99.00%
Hepatotoxicity + 0.7125 71.25%
skin sensitisation + 0.9522 95.22%
Respiratory toxicity - 0.7667 76.67%
Reproductive toxicity + 0.6333 63.33%
Mitochondrial toxicity - 0.9625 96.25%
Nephrotoxicity + 0.6184 61.84%
Acute Oral Toxicity (c) III 0.8646 86.46%
Estrogen receptor binding - 0.9636 96.36%
Androgen receptor binding - 0.7369 73.69%
Thyroid receptor binding - 0.9078 90.78%
Glucocorticoid receptor binding - 0.8860 88.60%
Aromatase binding - 0.8474 84.74%
PPAR gamma - 0.8653 86.53%
Honey bee toxicity - 0.9522 95.22%
Biodegradation + 0.5750 57.50%
Crustacea aquatic toxicity - 0.5400 54.00%
Fish aquatic toxicity + 0.9880 98.80%

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 86.58% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 86.35% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.72% 95.56%
CHEMBL1951 P21397 Monoamine oxidase A 84.57% 91.49%

Cross-Links

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PubChem 176983
NPASS NPC146522
LOTUS LTS0275561
wikiData Q27161428