6-Hydroxyimino-4-(hydroxymethyl)cyclohexa-2,4-dien-1-ol

Details

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Internal ID 75cef478-0d55-4bed-abb0-b9eb38299e27
Taxonomy Organic nitrogen compounds > Organonitrogen compounds > Oximes > Ketoximes
IUPAC Name 6-hydroxyimino-4-(hydroxymethyl)cyclohexa-2,4-dien-1-ol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C7H9NO3/c9-4-5-1-2-7(10)6(3-5)8-11/h1-3,7,9-11H,4H2
InChI Key WTRMKZGASMSMCW-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C7H9NO3
Molecular Weight 155.15 g/mol
Exact Mass 155.058243149 g/mol
Topological Polar Surface Area (TPSA) 73.10 Ų
XlogP 0.00
Atomic LogP (AlogP) -0.33
H-Bond Acceptor 4
H-Bond Donor 3
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 6-Hydroxyimino-4-(hydroxymethyl)cyclohexa-2,4-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 + 0.9053 90.53%
Caco-2 - 0.7043 70.43%
Blood Brain Barrier + 0.5871 58.71%
Human oral bioavailability + 0.5571 55.71%
Subcellular localzation Mitochondria 0.6260 62.60%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9428 94.28%
OATP1B3 inhibitior + 0.9445 94.45%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8088 80.88%
BSEP inhibitior - 0.9536 95.36%
P-glycoprotein inhibitior - 0.9792 97.92%
P-glycoprotein substrate - 0.8845 88.45%
CYP3A4 substrate - 0.6414 64.14%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8440 84.40%
CYP3A4 inhibition - 0.8036 80.36%
CYP2C9 inhibition - 0.7730 77.30%
CYP2C19 inhibition - 0.6489 64.89%
CYP2D6 inhibition - 0.8655 86.55%
CYP1A2 inhibition - 0.5662 56.62%
CYP2C8 inhibition - 0.9551 95.51%
CYP inhibitory promiscuity - 0.6688 66.88%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.6061 60.61%
Carcinogenicity (trinary) Non-required 0.5598 55.98%
Eye corrosion - 0.9534 95.34%
Eye irritation + 0.8472 84.72%
Skin irritation - 0.6336 63.36%
Skin corrosion - 0.8861 88.61%
Ames mutagenesis + 0.6346 63.46%
Human Ether-a-go-go-Related Gene inhibition - 0.8249 82.49%
Micronuclear + 0.5300 53.00%
Hepatotoxicity - 0.5000 50.00%
skin sensitisation - 0.6797 67.97%
Respiratory toxicity - 0.5000 50.00%
Reproductive toxicity + 0.6667 66.67%
Mitochondrial toxicity - 0.5625 56.25%
Nephrotoxicity - 0.7893 78.93%
Acute Oral Toxicity (c) III 0.5854 58.54%
Estrogen receptor binding - 0.7309 73.09%
Androgen receptor binding - 0.7619 76.19%
Thyroid receptor binding - 0.7572 75.72%
Glucocorticoid receptor binding - 0.5194 51.94%
Aromatase binding - 0.7785 77.85%
PPAR gamma - 0.8017 80.17%
Honey bee toxicity - 0.9141 91.41%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity - 0.6600 66.00%
Fish aquatic toxicity - 0.5749 57.49%

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 94.59% 91.11%
CHEMBL226 P30542 Adenosine A1 receptor 92.42% 95.93%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.69% 96.09%
CHEMBL2581 P07339 Cathepsin D 82.24% 98.95%
CHEMBL4040 P28482 MAP kinase ERK2 80.79% 83.82%

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 139588877
LOTUS LTS0183796
wikiData Q104200630