4-Hydroxyxylidine

Details

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Internal ID 69e188b0-9954-445b-9d01-a584199a4796
Taxonomy Benzenoids > Phenols > Cresols > Ortho cresols
IUPAC Name 4-amino-2,3-dimethylphenol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C8H11NO/c1-5-6(2)8(10)4-3-7(5)9/h3-4,10H,9H2,1-2H3
InChI Key UBKPLLYABUUFCE-UHFFFAOYSA-N
Popularity 24 references in papers

Physical and Chemical Properties

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Molecular Formula C8H11NO
Molecular Weight 137.18 g/mol
Exact Mass 137.084063974 g/mol
Topological Polar Surface Area (TPSA) 46.30 Ų
XlogP 0.90
Atomic LogP (AlogP) 1.59
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 0

Synonyms

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RefChem:517542
4-Amino-2,3-dimethylphenol
4-Amino-2,3-xylenol
3096-69-3
Phenol, 4-amino-2,3-dimethyl-
MFCD00070554
4-Hydroxy-2,3-dimethylaniline
NSC-143549
4-Amino-2,3-dimethyl-phenol
2,3-dimethyl-4-hydroxyaniline
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 4-Hydroxyxylidine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9937 99.37%
Caco-2 + 0.9154 91.54%
Blood Brain Barrier - 0.5750 57.50%
Human oral bioavailability + 0.6286 62.86%
Subcellular localzation Mitochondria 0.3736 37.36%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9445 94.45%
OATP1B3 inhibitior + 0.9651 96.51%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.9517 95.17%
P-glycoprotein inhibitior - 0.9898 98.98%
P-glycoprotein substrate - 0.9716 97.16%
CYP3A4 substrate - 0.7604 76.04%
CYP2C9 substrate - 0.6532 65.32%
CYP2D6 substrate + 0.4053 40.53%
CYP3A4 inhibition - 0.8010 80.10%
CYP2C9 inhibition - 0.6456 64.56%
CYP2C19 inhibition - 0.7304 73.04%
CYP2D6 inhibition - 0.9473 94.73%
CYP1A2 inhibition + 0.5303 53.03%
CYP2C8 inhibition - 0.9372 93.72%
CYP inhibitory promiscuity - 0.6709 67.09%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.6029 60.29%
Carcinogenicity (trinary) Non-required 0.5994 59.94%
Eye corrosion - 0.7582 75.82%
Eye irritation + 0.9893 98.93%
Skin irritation - 0.7463 74.63%
Skin corrosion - 0.8191 81.91%
Ames mutagenesis - 0.5100 51.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7440 74.40%
Micronuclear + 0.6200 62.00%
Hepatotoxicity + 0.7250 72.50%
skin sensitisation + 0.8514 85.14%
Respiratory toxicity - 0.8000 80.00%
Reproductive toxicity + 0.5889 58.89%
Mitochondrial toxicity - 0.5625 56.25%
Nephrotoxicity + 0.5134 51.34%
Acute Oral Toxicity (c) III 0.8107 81.07%
Estrogen receptor binding - 0.7531 75.31%
Androgen receptor binding - 0.5573 55.73%
Thyroid receptor binding - 0.6972 69.72%
Glucocorticoid receptor binding - 0.8428 84.28%
Aromatase binding - 0.8136 81.36%
PPAR gamma - 0.6434 64.34%
Honey bee toxicity - 0.9844 98.44%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity + 0.6000 60.00%
Fish aquatic toxicity + 0.6977 69.77%

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 92.56% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.11% 95.56%
CHEMBL3492 P49721 Proteasome Macropain subunit 88.02% 90.24%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 84.74% 99.15%
CHEMBL2041 P07949 Tyrosine-protein kinase receptor RET 80.14% 91.79%

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.
Schisandra chinensis

Cross-Links

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PubChem 76542
NPASS NPC97095