Limonen-4-ol

Details

Top
Internal ID f34eaed3-f6e0-45bd-9a7f-be1bd86cbb06
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids > Menthane monoterpenoids
IUPAC Name 4-methyl-1-prop-1-en-2-ylcyclohex-3-en-1-ol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C10H16O/c1-8(2)10(11)6-4-9(3)5-7-10/h4,11H,1,5-7H2,2-3H3
InChI Key OVKDFILSBMEKLT-UHFFFAOYSA-N
Popularity 19 references in papers

Physical and Chemical Properties

Top
Molecular Formula C10H16O
Molecular Weight 152.23 g/mol
Exact Mass 152.120115130 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 2.10
Atomic LogP (AlogP) 2.42
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

Top
Limonen-4-ol
RefChem:1088468
p-Mentha-1,8-dien-4-ol
4-Methyl-1-(prop-1-en-2-yl)cyclohex-3-enol
4-methyl-1-prop-1-en-2-ylcyclohex-3-en-1-ol
1,8-Menthadien-4-ol
4-methyl-1-(prop-1-en-2-yl)cyclohex-3-en-1-ol
Limonene-4-ol
1,8-Menthadiene-4-ol
p-1,8-Menthadien-4-ol
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

Top
2D Structure of Limonen-4-ol

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9955 99.55%
Caco-2 + 0.9114 91.14%
Blood Brain Barrier + 0.7000 70.00%
Human oral bioavailability + 0.5429 54.29%
Subcellular localzation Lysosomes 0.4973 49.73%
OATP2B1 inhibitior - 0.8492 84.92%
OATP1B1 inhibitior + 0.9609 96.09%
OATP1B3 inhibitior + 0.9235 92.35%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior - 0.9157 91.57%
P-glycoprotein inhibitior - 0.9800 98.00%
P-glycoprotein substrate - 0.9362 93.62%
CYP3A4 substrate - 0.5942 59.42%
CYP2C9 substrate - 0.7899 78.99%
CYP2D6 substrate - 0.7511 75.11%
CYP3A4 inhibition - 0.8204 82.04%
CYP2C9 inhibition - 0.8568 85.68%
CYP2C19 inhibition - 0.8552 85.52%
CYP2D6 inhibition - 0.9417 94.17%
CYP1A2 inhibition - 0.8496 84.96%
CYP2C8 inhibition - 0.9405 94.05%
CYP inhibitory promiscuity - 0.9435 94.35%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.8228 82.28%
Carcinogenicity (trinary) Non-required 0.5781 57.81%
Eye corrosion - 0.8652 86.52%
Eye irritation + 0.9721 97.21%
Skin irritation + 0.7120 71.20%
Skin corrosion - 0.9556 95.56%
Ames mutagenesis - 0.8200 82.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7498 74.98%
Micronuclear - 0.9900 99.00%
Hepatotoxicity + 0.7463 74.63%
skin sensitisation + 0.8735 87.35%
Respiratory toxicity - 0.6444 64.44%
Reproductive toxicity - 0.6182 61.82%
Mitochondrial toxicity - 0.7875 78.75%
Nephrotoxicity + 0.5000 50.00%
Acute Oral Toxicity (c) III 0.8489 84.89%
Estrogen receptor binding - 0.9449 94.49%
Androgen receptor binding - 0.7465 74.65%
Thyroid receptor binding - 0.9039 90.39%
Glucocorticoid receptor binding - 0.7755 77.55%
Aromatase binding - 0.8261 82.61%
PPAR gamma - 0.7996 79.96%
Honey bee toxicity - 0.8952 89.52%
Biodegradation + 0.8250 82.50%
Crustacea aquatic toxicity - 0.5400 54.00%
Fish aquatic toxicity + 0.9565 95.65%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.16% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.78% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 82.45% 95.56%
CHEMBL5966 P55899 IgG receptor FcRn large subunit p51 81.17% 90.93%
CHEMBL4208 P20618 Proteasome component C5 80.47% 90.00%

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.
Sideritis tragoriganum
Zanthoxylum bungeanum
Zanthoxylum schinifolium

Cross-Links

Top
PubChem 527428
NPASS NPC266147
LOTUS LTS0071786
wikiData Q82102431