2-Methyl-6-(4-methylcyclohex-3-en-1-yl)hepta-2,5-dien-1-ol

Details

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Internal ID 754258df-d3e0-4a8b-9828-d636e4f76710
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name 2-methyl-6-(4-methylcyclohex-3-en-1-yl)hepta-2,5-dien-1-ol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H24O/c1-12-7-9-15(10-8-12)14(3)6-4-5-13(2)11-16/h5-7,15-16H,4,8-11H2,1-3H3
InChI Key CUXGFNUZZPYJNJ-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H24O
Molecular Weight 220.35 g/mol
Exact Mass 220.182715385 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 3.90
Atomic LogP (AlogP) 4.01
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2-Methyl-6-(4-methylcyclohex-3-en-1-yl)hepta-2,5-dien-1-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9879 98.79%
Caco-2 + 0.8568 85.68%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.5286 52.86%
Subcellular localzation Lysosomes 0.6996 69.96%
OATP2B1 inhibitior - 0.8542 85.42%
OATP1B1 inhibitior + 0.9369 93.69%
OATP1B3 inhibitior + 0.9110 91.10%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior - 0.7798 77.98%
P-glycoprotein inhibitior - 0.9776 97.76%
P-glycoprotein substrate - 0.8716 87.16%
CYP3A4 substrate - 0.5567 55.67%
CYP2C9 substrate - 0.6591 65.91%
CYP2D6 substrate - 0.7543 75.43%
CYP3A4 inhibition - 0.7246 72.46%
CYP2C9 inhibition - 0.8606 86.06%
CYP2C19 inhibition - 0.8424 84.24%
CYP2D6 inhibition - 0.8760 87.60%
CYP1A2 inhibition - 0.8098 80.98%
CYP2C8 inhibition - 0.8516 85.16%
CYP inhibitory promiscuity - 0.7091 70.91%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.8228 82.28%
Carcinogenicity (trinary) Non-required 0.6361 63.61%
Eye corrosion - 0.7003 70.03%
Eye irritation - 0.7484 74.84%
Skin irritation + 0.5441 54.41%
Skin corrosion - 0.9695 96.95%
Ames mutagenesis - 0.9000 90.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3681 36.81%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.5271 52.71%
skin sensitisation + 0.8532 85.32%
Respiratory toxicity - 0.7000 70.00%
Reproductive toxicity - 0.6556 65.56%
Mitochondrial toxicity - 0.8875 88.75%
Nephrotoxicity - 0.6446 64.46%
Acute Oral Toxicity (c) III 0.9137 91.37%
Estrogen receptor binding - 0.8444 84.44%
Androgen receptor binding - 0.8265 82.65%
Thyroid receptor binding - 0.6071 60.71%
Glucocorticoid receptor binding - 0.6104 61.04%
Aromatase binding - 0.6642 66.42%
PPAR gamma + 0.6729 67.29%
Honey bee toxicity - 0.9631 96.31%
Biodegradation - 0.5250 52.50%
Crustacea aquatic toxicity - 0.6300 63.00%
Fish aquatic toxicity + 0.9734 97.34%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.23% 91.11%
CHEMBL2581 P07339 Cathepsin D 90.26% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.90% 96.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 85.23% 100.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.41% 95.56%
CHEMBL3137262 O60341 LSD1/CoREST complex 84.22% 97.09%
CHEMBL3401 O75469 Pregnane X receptor 82.53% 94.73%
CHEMBL253 P34972 Cannabinoid CB2 receptor 80.20% 97.25%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 73803944
LOTUS LTS0198208
wikiData Q104970559