4-Bromo-3-(hydroxymethyl)cyclohexa-1,5-diene-1,4-diol

Details

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Internal ID ab2ab34e-b76b-4667-9b0f-5d314ee7d7cb
Taxonomy Organic oxygen compounds > Organooxygen compounds > Enols
IUPAC Name 4-bromo-3-(hydroxymethyl)cyclohexa-1,5-diene-1,4-diol
SMILES (Canonical) C1=CC(C(C=C1O)CO)(O)Br
SMILES (Isomeric) C1=CC(C(C=C1O)CO)(O)Br
InChI InChI=1S/C7H9BrO3/c8-7(11)2-1-6(10)3-5(7)4-9/h1-3,5,9-11H,4H2
InChI Key AIBZCQINGHNFDT-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C7H9BrO3
Molecular Weight 221.05 g/mol
Exact Mass 219.97351 g/mol
Topological Polar Surface Area (TPSA) 60.70 Ų
XlogP 0.80
Atomic LogP (AlogP) 0.69
H-Bond Acceptor 3
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 4-Bromo-3-(hydroxymethyl)cyclohexa-1,5-diene-1,4-diol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8836 88.36%
Caco-2 + 0.6840 68.40%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability + 0.5571 55.71%
Subcellular localzation Mitochondria 0.7340 73.40%
OATP2B1 inhibitior - 0.8582 85.82%
OATP1B1 inhibitior + 0.9199 91.99%
OATP1B3 inhibitior + 0.9525 95.25%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9088 90.88%
BSEP inhibitior - 0.9355 93.55%
P-glycoprotein inhibitior - 0.9774 97.74%
P-glycoprotein substrate - 0.8804 88.04%
CYP3A4 substrate - 0.6293 62.93%
CYP2C9 substrate - 0.6000 60.00%
CYP2D6 substrate - 0.8499 84.99%
CYP3A4 inhibition - 0.7070 70.70%
CYP2C9 inhibition - 0.6010 60.10%
CYP2C19 inhibition - 0.5716 57.16%
CYP2D6 inhibition - 0.8945 89.45%
CYP1A2 inhibition - 0.6261 62.61%
CYP2C8 inhibition - 0.9045 90.45%
CYP inhibitory promiscuity - 0.5101 51.01%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.7886 78.86%
Carcinogenicity (trinary) Non-required 0.5708 57.08%
Eye corrosion - 0.9232 92.32%
Eye irritation + 0.8388 83.88%
Skin irritation - 0.6098 60.98%
Skin corrosion - 0.8676 86.76%
Ames mutagenesis - 0.7000 70.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7575 75.75%
Micronuclear - 0.7641 76.41%
Hepatotoxicity - 0.5625 56.25%
skin sensitisation - 0.5985 59.85%
Respiratory toxicity + 0.5444 54.44%
Reproductive toxicity + 0.5222 52.22%
Mitochondrial toxicity - 0.6000 60.00%
Nephrotoxicity + 0.5143 51.43%
Acute Oral Toxicity (c) III 0.6188 61.88%
Estrogen receptor binding - 0.8435 84.35%
Androgen receptor binding - 0.7858 78.58%
Thyroid receptor binding - 0.7551 75.51%
Glucocorticoid receptor binding - 0.6623 66.23%
Aromatase binding - 0.7270 72.70%
PPAR gamma - 0.7177 71.77%
Honey bee toxicity - 0.9466 94.66%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity - 0.6200 62.00%
Fish aquatic toxicity + 0.8346 83.46%

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 96.62% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.30% 96.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 90.36% 94.45%
CHEMBL1937 Q92769 Histone deacetylase 2 87.15% 94.75%
CHEMBL3137262 O60341 LSD1/CoREST complex 85.71% 97.09%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 81.75% 86.92%

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 145915962
LOTUS LTS0135553
wikiData Q105095537