p-Mentha-2,4-diene

Details

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Internal ID b1df8d09-1e2f-4e13-8f53-4e742349a001
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids > Menthane monoterpenoids
IUPAC Name 5-methyl-2-propan-2-ylcyclohexa-1,3-diene
SMILES (Canonical) CC1CC=C(C=C1)C(C)C
SMILES (Isomeric) CC1CC=C(C=C1)C(C)C
InChI InChI=1S/C10H16/c1-8(2)10-6-4-9(3)5-7-10/h4,6-9H,5H2,1-3H3
InChI Key AAIXZDBTEWDLSG-UHFFFAOYSA-N
Popularity 14 references in papers

Physical and Chemical Properties

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Molecular Formula C10H16
Molecular Weight 136.23 g/mol
Exact Mass 136.125200510 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 3.20
Atomic LogP (AlogP) 3.16
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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2,4-p-Menthadiene
38QSP402UI
586-68-5
3-Cyclohexadiene, 5-methyl-2-(1-methylethyl)-
Cyclohexanol, 5-methyl-2-(1-methylethyl)-, (1alpha,2alpha,5alpha)-
5-methyl-2-(propan-2-yl)cyclohexa-1,3-diene
RefChem:1094199
.delta.-Terpinene
Menthol, cis-1,3,cis-1,4-
UNII-38QSP402UI
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-2,4-diene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9924 99.24%
Caco-2 + 0.8806 88.06%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.5857 58.57%
Subcellular localzation Lysosomes 0.5194 51.94%
OATP2B1 inhibitior - 0.8649 86.49%
OATP1B1 inhibitior + 0.9695 96.95%
OATP1B3 inhibitior + 0.9231 92.31%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.8576 85.76%
P-glycoprotein inhibitior - 0.9830 98.30%
P-glycoprotein substrate - 0.9342 93.42%
CYP3A4 substrate - 0.6984 69.84%
CYP2C9 substrate - 0.8164 81.64%
CYP2D6 substrate - 0.7751 77.51%
CYP3A4 inhibition - 0.8943 89.43%
CYP2C9 inhibition - 0.8766 87.66%
CYP2C19 inhibition - 0.9093 90.93%
CYP2D6 inhibition - 0.9139 91.39%
CYP1A2 inhibition - 0.8125 81.25%
CYP2C8 inhibition - 0.9879 98.79%
CYP inhibitory promiscuity - 0.6481 64.81%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5464 54.64%
Carcinogenicity (trinary) Warning 0.6226 62.26%
Eye corrosion + 0.7745 77.45%
Eye irritation + 0.9791 97.91%
Skin irritation + 0.7673 76.73%
Skin corrosion - 0.9344 93.44%
Ames mutagenesis - 0.8300 83.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6630 66.30%
Micronuclear - 0.9800 98.00%
Hepatotoxicity + 0.5500 55.00%
skin sensitisation + 0.9520 95.20%
Respiratory toxicity + 0.5222 52.22%
Reproductive toxicity + 0.6222 62.22%
Mitochondrial toxicity - 0.7800 78.00%
Nephrotoxicity - 0.7136 71.36%
Acute Oral Toxicity (c) III 0.8178 81.78%
Estrogen receptor binding - 0.9786 97.86%
Androgen receptor binding - 0.8429 84.29%
Thyroid receptor binding - 0.8733 87.33%
Glucocorticoid receptor binding - 0.8426 84.26%
Aromatase binding - 0.9008 90.08%
PPAR gamma - 0.9201 92.01%
Honey bee toxicity - 0.9563 95.63%
Biodegradation + 0.5250 52.50%
Crustacea aquatic toxicity + 0.6200 62.00%
Fish aquatic toxicity + 0.9776 97.76%

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 92.24% 97.25%
CHEMBL2581 P07339 Cathepsin D 89.04% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 88.77% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.17% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.15% 95.56%
CHEMBL3359 P21462 Formyl peptide receptor 1 81.71% 93.56%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 80.82% 96.47%

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.
Platycladus orientalis
Teucrium bidentatum

Cross-Links

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PubChem 6428962
NPASS NPC30032