Alcalinaphenol D

Details

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Internal ID 57328e0a-dbfa-4fd8-87d4-e3737bbc2941
Taxonomy Benzenoids > Phenols > Methoxyphenols
IUPAC Name 4-bromo-3-methoxy-5-methylbenzene-1,2-diol
SMILES (Canonical) CC1=CC(=C(C(=C1Br)OC)O)O
SMILES (Isomeric) CC1=CC(=C(C(=C1Br)OC)O)O
InChI InChI=1S/C8H9BrO3/c1-4-3-5(10)7(11)8(12-2)6(4)9/h3,10-11H,1-2H3
InChI Key YXINKIWRWMPNQA-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C8H9BrO3
Molecular Weight 233.06 g/mol
Exact Mass 231.97351 g/mol
Topological Polar Surface Area (TPSA) 49.70 Ų
XlogP 2.20
Atomic LogP (AlogP) 2.18
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

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4-Bromo-3-methoxy-5-methylbenzene-1,2-diol
920008-54-4
DTXSID40582714

2D Structure

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2D Structure of Alcalinaphenol D

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9799 97.99%
Caco-2 - 0.6274 62.74%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability + 0.6571 65.71%
Subcellular localzation Mitochondria 0.8341 83.41%
OATP2B1 inhibitior - 0.8596 85.96%
OATP1B1 inhibitior + 0.9383 93.83%
OATP1B3 inhibitior + 0.9687 96.87%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.9384 93.84%
P-glycoprotein inhibitior - 0.9600 96.00%
P-glycoprotein substrate - 0.9799 97.99%
CYP3A4 substrate - 0.6596 65.96%
CYP2C9 substrate - 0.7739 77.39%
CYP2D6 substrate - 0.6684 66.84%
CYP3A4 inhibition - 0.9100 91.00%
CYP2C9 inhibition - 0.7143 71.43%
CYP2C19 inhibition - 0.5410 54.10%
CYP2D6 inhibition - 0.8991 89.91%
CYP1A2 inhibition + 0.5763 57.63%
CYP2C8 inhibition - 0.7303 73.03%
CYP inhibitory promiscuity - 0.6267 62.67%
UGT catelyzed + 1.0000 100.00%
Carcinogenicity (binary) - 0.7126 71.26%
Carcinogenicity (trinary) Non-required 0.4402 44.02%
Eye corrosion + 0.4865 48.65%
Eye irritation + 0.9667 96.67%
Skin irritation + 0.5610 56.10%
Skin corrosion - 0.8044 80.44%
Ames mutagenesis - 0.8064 80.64%
Human Ether-a-go-go-Related Gene inhibition - 0.7032 70.32%
Micronuclear + 0.6333 63.33%
Hepatotoxicity + 0.6680 66.80%
skin sensitisation + 0.5537 55.37%
Respiratory toxicity - 0.6333 63.33%
Reproductive toxicity + 0.7778 77.78%
Mitochondrial toxicity - 0.7000 70.00%
Nephrotoxicity - 0.7909 79.09%
Acute Oral Toxicity (c) III 0.6896 68.96%
Estrogen receptor binding - 0.4787 47.87%
Androgen receptor binding - 0.5961 59.61%
Thyroid receptor binding - 0.6218 62.18%
Glucocorticoid receptor binding - 0.7242 72.42%
Aromatase binding - 0.8130 81.30%
PPAR gamma - 0.5873 58.73%
Honey bee toxicity - 0.9594 95.94%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity + 0.6300 63.00%
Fish aquatic toxicity + 0.9344 93.44%

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 97.77% 91.11%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 90.06% 94.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.88% 95.56%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 89.80% 99.15%
CHEMBL215 P09917 Arachidonate 5-lipoxygenase 85.09% 92.68%
CHEMBL3401 O75469 Pregnane X receptor 84.58% 94.73%
CHEMBL1293249 Q13887 Kruppel-like factor 5 80.87% 86.33%
CHEMBL241 Q14432 Phosphodiesterase 3A 80.10% 92.94%

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.
There are no matching plants.

Cross-Links

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PubChem 16099547
LOTUS LTS0038168
wikiData Q77513043