4-(2-Aminoethyl)phenol;hydron

Details

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Internal ID 01a54ba7-21e4-4a94-88ea-135809f0c0f4
Taxonomy Benzenoids > Benzene and substituted derivatives > Phenethylamines
IUPAC Name 4-(2-aminoethyl)phenol;hydron
SMILES (Canonical) [H+].C1=CC(=CC=C1CCN)O
SMILES (Isomeric) [H+].C1=CC(=CC=C1CCN)O
InChI InChI=1S/C8H11NO/c9-6-5-7-1-3-8(10)4-2-7/h1-4,10H,5-6,9H2/p+1
InChI Key DZGWFCGJZKJUFP-UHFFFAOYSA-O
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C8H12NO+
Molecular Weight 138.19 g/mol
Exact Mass 138.091889006 g/mol
Topological Polar Surface Area (TPSA) 46.20 Ų
XlogP 0.00
Atomic LogP (AlogP) 1.01
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 4-(2-Aminoethyl)phenol;hydron

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9833 98.33%
Caco-2 + 0.9637 96.37%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability - 0.7143 71.43%
Subcellular localzation Lysosomes 0.5700 57.00%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9411 94.11%
OATP1B3 inhibitior + 0.9518 95.18%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.6500 65.00%
BSEP inhibitior - 0.9345 93.45%
P-glycoprotein inhibitior - 0.9893 98.93%
P-glycoprotein substrate - 0.8774 87.74%
CYP3A4 substrate - 0.7626 76.26%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate + 0.4789 47.89%
CYP3A4 inhibition - 0.8844 88.44%
CYP2C9 inhibition - 0.9292 92.92%
CYP2C19 inhibition - 0.9037 90.37%
CYP2D6 inhibition - 0.9119 91.19%
CYP1A2 inhibition - 0.9019 90.19%
CYP2C8 inhibition + 0.6781 67.81%
CYP inhibitory promiscuity - 0.8383 83.83%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.6110 61.10%
Carcinogenicity (trinary) Non-required 0.7166 71.66%
Eye corrosion + 0.8005 80.05%
Eye irritation + 0.9442 94.42%
Skin irritation + 0.7050 70.50%
Skin corrosion + 0.7621 76.21%
Ames mutagenesis - 0.7100 71.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8152 81.52%
Micronuclear - 0.7000 70.00%
Hepatotoxicity - 0.5500 55.00%
skin sensitisation - 0.5997 59.97%
Respiratory toxicity + 0.6444 64.44%
Reproductive toxicity + 0.5556 55.56%
Mitochondrial toxicity + 0.8250 82.50%
Nephrotoxicity - 0.8079 80.79%
Acute Oral Toxicity (c) II 0.5923 59.23%
Estrogen receptor binding - 0.6992 69.92%
Androgen receptor binding - 0.5288 52.88%
Thyroid receptor binding - 0.7864 78.64%
Glucocorticoid receptor binding - 0.7783 77.83%
Aromatase binding - 0.8127 81.27%
PPAR gamma - 0.6713 67.13%
Honey bee toxicity - 0.9388 93.88%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity + 0.6100 61.00%
Fish aquatic toxicity - 0.9435 94.35%

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 94.08% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.89% 96.09%
CHEMBL242 Q92731 Estrogen receptor beta 87.77% 98.35%
CHEMBL3492 P49721 Proteasome Macropain subunit 87.41% 90.24%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 86.97% 94.45%
CHEMBL3230 O95977 Sphingosine 1-phosphate receptor Edg-6 86.31% 94.01%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.50% 99.17%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 83.34% 96.95%
CHEMBL3038469 P24941 CDK2/Cyclin A 82.28% 91.38%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 81.60% 91.71%
CHEMBL4101 P17612 cAMP-dependent protein kinase alpha-catalytic subunit 80.63% 82.86%
CHEMBL4581 P52732 Kinesin-like protein 1 80.42% 93.18%
CHEMBL2581 P07339 Cathepsin D 80.34% 98.95%

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.
Allium victorialis
Capsella bursa-pastoris
Chelidonium majus
Glycine max
Hordeum vulgare
Lophophora williamsii
Silybum marianum
Typha domingensis
Viscum album

Cross-Links

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PubChem 67458472
NPASS NPC125731