3-Methyl-1-prop-1-en-2-ylcyclohex-3-en-1-ol

Details

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Internal ID efdbc207-0f3a-481d-9caa-8349ba3c9a3c
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids > Monocyclic monoterpenoids
IUPAC Name 3-methyl-1-prop-1-en-2-ylcyclohex-3-en-1-ol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C10H16O/c1-8(2)10(11)6-4-5-9(3)7-10/h5,11H,1,4,6-7H2,2-3H3
InChI Key WQABFSITNCYDBD-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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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

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There are no found synonyms.

2D Structure

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2D Structure of 3-Methyl-1-prop-1-en-2-ylcyclohex-3-en-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 + 0.9955 99.55%
Caco-2 + 0.9031 90.31%
Blood Brain Barrier + 0.7000 70.00%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Lysosomes 0.4973 49.73%
OATP2B1 inhibitior - 0.8478 84.78%
OATP1B1 inhibitior + 0.9692 96.92%
OATP1B3 inhibitior + 0.9235 92.35%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior - 0.8798 87.98%
P-glycoprotein inhibitior - 0.9748 97.48%
P-glycoprotein substrate - 0.9434 94.34%
CYP3A4 substrate - 0.6038 60.38%
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 - 0.9406 94.06%
CYP inhibitory promiscuity - 0.9435 94.35%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.8228 82.28%
Carcinogenicity (trinary) Non-required 0.5781 57.81%
Eye corrosion - 0.8652 86.52%
Eye irritation + 0.9827 98.27%
Skin irritation + 0.7120 71.20%
Skin corrosion - 0.9556 95.56%
Ames mutagenesis - 0.7900 79.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5823 58.23%
Micronuclear - 0.9900 99.00%
Hepatotoxicity + 0.6090 60.90%
skin sensitisation + 0.8735 87.35%
Respiratory toxicity - 0.7000 70.00%
Reproductive toxicity - 0.6182 61.82%
Mitochondrial toxicity - 0.7875 78.75%
Nephrotoxicity + 0.7145 71.45%
Acute Oral Toxicity (c) III 0.8489 84.89%
Estrogen receptor binding - 0.9644 96.44%
Androgen receptor binding - 0.8111 81.11%
Thyroid receptor binding - 0.8946 89.46%
Glucocorticoid receptor binding - 0.9081 90.81%
Aromatase binding - 0.9297 92.97%
PPAR gamma - 0.7739 77.39%
Honey bee toxicity - 0.9306 93.06%
Biodegradation + 0.7000 70.00%
Crustacea aquatic toxicity - 0.5500 55.00%
Fish aquatic toxicity + 0.9565 95.65%

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 93.59% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.46% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 86.80% 97.25%
CHEMBL4208 P20618 Proteasome component C5 85.65% 90.00%
CHEMBL3492 P49721 Proteasome Macropain subunit 81.52% 90.24%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 80.84% 95.56%

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.
Cannabis sativa

Cross-Links

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PubChem 101409170
LOTUS LTS0270867
wikiData Q105310291