6-Hydroxy-3-(hydroxymethyl)-2,4,4-trimethylcyclohexa-2,5-dien-1-one

Details

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Internal ID c23dedc3-6f16-40ac-a25e-897b2ccfeda1
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Cyclic ketones
IUPAC Name 6-hydroxy-3-(hydroxymethyl)-2,4,4-trimethylcyclohexa-2,5-dien-1-one
SMILES (Canonical) CC1=C(C(C=C(C1=O)O)(C)C)CO
SMILES (Isomeric) CC1=C(C(C=C(C1=O)O)(C)C)CO
InChI InChI=1S/C10H14O3/c1-6-7(5-11)10(2,3)4-8(12)9(6)13/h4,11-12H,5H2,1-3H3
InChI Key RDTZVJXIFNPDIG-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C10H14O3
Molecular Weight 182.22 g/mol
Exact Mass 182.094294304 g/mol
Topological Polar Surface Area (TPSA) 57.50 Ų
XlogP 0.90
Atomic LogP (AlogP) 1.35
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

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211107-45-8
6-Hydroxy-3-(hydroxymethyl)-2,4,4-trimethylcyclohexa-2,5-dien-1-one
DTXSID80631492

2D Structure

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2D Structure of 6-Hydroxy-3-(hydroxymethyl)-2,4,4-trimethylcyclohexa-2,5-dien-1-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9938 99.38%
Caco-2 + 0.5839 58.39%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability + 0.6143 61.43%
Subcellular localzation Mitochondria 0.8435 84.35%
OATP2B1 inhibitior - 0.8580 85.80%
OATP1B1 inhibitior + 0.8995 89.95%
OATP1B3 inhibitior + 0.9355 93.55%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.9314 93.14%
P-glycoprotein inhibitior - 0.9667 96.67%
P-glycoprotein substrate - 0.9467 94.67%
CYP3A4 substrate - 0.5899 58.99%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8908 89.08%
CYP3A4 inhibition - 0.8471 84.71%
CYP2C9 inhibition - 0.7895 78.95%
CYP2C19 inhibition - 0.7830 78.30%
CYP2D6 inhibition - 0.8781 87.81%
CYP1A2 inhibition - 0.7168 71.68%
CYP2C8 inhibition - 0.9800 98.00%
CYP inhibitory promiscuity - 0.7042 70.42%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.7367 73.67%
Carcinogenicity (trinary) Non-required 0.6790 67.90%
Eye corrosion - 0.9451 94.51%
Eye irritation + 0.8816 88.16%
Skin irritation - 0.5710 57.10%
Skin corrosion - 0.8836 88.36%
Ames mutagenesis - 0.5944 59.44%
Human Ether-a-go-go-Related Gene inhibition - 0.7132 71.32%
Micronuclear - 0.8500 85.00%
Hepatotoxicity + 0.5185 51.85%
skin sensitisation + 0.6564 65.64%
Respiratory toxicity - 0.6111 61.11%
Reproductive toxicity + 0.5556 55.56%
Mitochondrial toxicity - 0.5500 55.00%
Nephrotoxicity + 0.7644 76.44%
Acute Oral Toxicity (c) III 0.6475 64.75%
Estrogen receptor binding - 0.8086 80.86%
Androgen receptor binding - 0.7950 79.50%
Thyroid receptor binding - 0.7508 75.08%
Glucocorticoid receptor binding - 0.7593 75.93%
Aromatase binding - 0.7497 74.97%
PPAR gamma - 0.6348 63.48%
Honey bee toxicity - 0.9625 96.25%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.7600 76.00%
Fish aquatic toxicity + 0.8608 86.08%

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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.49% 95.56%
CHEMBL2581 P07339 Cathepsin D 91.57% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.87% 91.11%
CHEMBL4040 P28482 MAP kinase ERK2 88.30% 83.82%
CHEMBL1937 Q92769 Histone deacetylase 2 87.09% 94.75%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 81.04% 96.09%
CHEMBL3401 O75469 Pregnane X receptor 80.29% 94.73%

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 23244089
NPASS NPC279221
LOTUS LTS0024070
wikiData Q82538693