4-Ethenyl-3,5,5-trimethylcyclohex-3-en-1-ol

Details

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Internal ID 6603b87b-0103-4d0f-b7d2-0d8ada2a4896
Taxonomy Organic oxygen compounds > Organooxygen compounds > Alcohols and polyols > Secondary alcohols
IUPAC Name 4-ethenyl-3,5,5-trimethylcyclohex-3-en-1-ol
SMILES (Canonical) CC1=C(C(CC(C1)O)(C)C)C=C
SMILES (Isomeric) CC1=C(C(CC(C1)O)(C)C)C=C
InChI InChI=1S/C11H18O/c1-5-10-8(2)6-9(12)7-11(10,3)4/h5,9,12H,1,6-7H2,2-4H3
InChI Key JBNNEBXFMFDBSS-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C11H18O
Molecular Weight 166.26 g/mol
Exact Mass 166.135765193 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 2.20
Atomic LogP (AlogP) 2.67
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 4-Ethenyl-3,5,5-trimethylcyclohex-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 + 0.9925 99.25%
Caco-2 + 0.9390 93.90%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability + 0.5429 54.29%
Subcellular localzation Lysosomes 0.5201 52.01%
OATP2B1 inhibitior - 0.8537 85.37%
OATP1B1 inhibitior + 0.9119 91.19%
OATP1B3 inhibitior + 0.8898 88.98%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.8901 89.01%
P-glycoprotein inhibitior - 0.9716 97.16%
P-glycoprotein substrate - 0.9285 92.85%
CYP3A4 substrate - 0.5399 53.99%
CYP2C9 substrate - 0.8262 82.62%
CYP2D6 substrate - 0.7495 74.95%
CYP3A4 inhibition - 0.8435 84.35%
CYP2C9 inhibition - 0.8562 85.62%
CYP2C19 inhibition - 0.6992 69.92%
CYP2D6 inhibition - 0.9531 95.31%
CYP1A2 inhibition - 0.8747 87.47%
CYP2C8 inhibition - 0.8965 89.65%
CYP inhibitory promiscuity - 0.8722 87.22%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.6852 68.52%
Carcinogenicity (trinary) Non-required 0.6021 60.21%
Eye corrosion - 0.8671 86.71%
Eye irritation + 0.9145 91.45%
Skin irritation + 0.6525 65.25%
Skin corrosion - 0.9043 90.43%
Ames mutagenesis - 0.7591 75.91%
Human Ether-a-go-go-Related Gene inhibition - 0.7393 73.93%
Micronuclear - 0.9600 96.00%
Hepatotoxicity - 0.5673 56.73%
skin sensitisation + 0.8947 89.47%
Respiratory toxicity - 0.5222 52.22%
Reproductive toxicity - 0.5778 57.78%
Mitochondrial toxicity - 0.7500 75.00%
Nephrotoxicity + 0.4872 48.72%
Acute Oral Toxicity (c) III 0.8498 84.98%
Estrogen receptor binding - 0.9377 93.77%
Androgen receptor binding - 0.8215 82.15%
Thyroid receptor binding - 0.7530 75.30%
Glucocorticoid receptor binding - 0.8583 85.83%
Aromatase binding - 0.7544 75.44%
PPAR gamma - 0.6581 65.81%
Honey bee toxicity - 0.8241 82.41%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity - 0.5000 50.00%
Fish aquatic toxicity + 0.9391 93.91%

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 92.73% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.09% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.41% 95.56%
CHEMBL240 Q12809 HERG 84.00% 89.76%
CHEMBL2581 P07339 Cathepsin D 82.52% 98.95%
CHEMBL221 P23219 Cyclooxygenase-1 80.91% 90.17%
CHEMBL1951 P21397 Monoamine oxidase A 80.80% 91.49%

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.
Crocus sativus

Cross-Links

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PubChem 91753281
NPASS NPC287109