(S)-1-(4-(aminomethyl)phenyl)ethan-1-ol

Details

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Internal ID 7c5f06fd-9c18-4523-9e67-e4097bb88092
Taxonomy Benzenoids > Benzene and substituted derivatives > Phenylmethylamines
IUPAC Name (1S)-1-[4-(aminomethyl)phenyl]ethanol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C9H13NO/c1-7(11)9-4-2-8(6-10)3-5-9/h2-5,7,11H,6,10H2,1H3/t7-/m0/s1
InChI Key RIYYBTSTPIEMBD-ZETCQYMHSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C9H13NO
Molecular Weight 151.21 g/mol
Exact Mass 151.099714038 g/mol
Topological Polar Surface Area (TPSA) 46.30 Ų
XlogP 0.30
Atomic LogP (AlogP) 1.20
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 2

Synonyms

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(S)-1-(4-(aminomethyl)phenyl)ethan-1-ol
214760-48-2

2D Structure

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2D Structure of (S)-1-(4-(aminomethyl)phenyl)ethan-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 + 0.9913 99.13%
Caco-2 + 0.8793 87.93%
Blood Brain Barrier + 0.7500 75.00%
Human oral bioavailability + 0.6571 65.71%
Subcellular localzation Lysosomes 0.7489 74.89%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9659 96.59%
OATP1B3 inhibitior + 0.9596 95.96%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.9523 95.23%
P-glycoprotein inhibitior - 0.9822 98.22%
P-glycoprotein substrate - 0.8037 80.37%
CYP3A4 substrate - 0.8088 80.88%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate + 0.5263 52.63%
CYP3A4 inhibition - 0.8466 84.66%
CYP2C9 inhibition - 0.8586 85.86%
CYP2C19 inhibition - 0.8881 88.81%
CYP2D6 inhibition - 0.9307 93.07%
CYP1A2 inhibition - 0.7427 74.27%
CYP2C8 inhibition - 0.9758 97.58%
CYP inhibitory promiscuity - 0.8116 81.16%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) + 0.5200 52.00%
Carcinogenicity (trinary) Non-required 0.6782 67.82%
Eye corrosion + 0.9430 94.30%
Eye irritation + 0.9153 91.53%
Skin irritation + 0.6791 67.91%
Skin corrosion + 0.9329 93.29%
Ames mutagenesis - 0.7770 77.70%
Human Ether-a-go-go-Related Gene inhibition - 0.7889 78.89%
Micronuclear - 0.7900 79.00%
Hepatotoxicity - 0.6378 63.78%
skin sensitisation + 0.5289 52.89%
Respiratory toxicity + 0.8222 82.22%
Reproductive toxicity - 0.6667 66.67%
Mitochondrial toxicity + 0.7750 77.50%
Nephrotoxicity - 0.8873 88.73%
Acute Oral Toxicity (c) II 0.5052 50.52%
Estrogen receptor binding - 0.9181 91.81%
Androgen receptor binding - 0.7283 72.83%
Thyroid receptor binding - 0.8427 84.27%
Glucocorticoid receptor binding - 0.8662 86.62%
Aromatase binding - 0.8197 81.97%
PPAR gamma - 0.8496 84.96%
Honey bee toxicity - 0.9512 95.12%
Biodegradation - 0.5000 50.00%
Crustacea aquatic toxicity - 0.6800 68.00%
Fish aquatic toxicity - 0.9037 90.37%

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
CHEMBL3492 P49721 Proteasome Macropain subunit 98.20% 90.24%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.21% 96.09%
CHEMBL2581 P07339 Cathepsin D 95.87% 98.95%
CHEMBL1907594 P30926 Neuronal acetylcholine receptor; alpha3/beta4 84.88% 97.23%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 83.85% 94.45%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.73% 95.89%
CHEMBL3401 O75469 Pregnane X receptor 81.70% 94.73%
CHEMBL3830 Q2M2I8 Adaptor-associated kinase 81.54% 83.10%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 81.11% 95.56%
CHEMBL253 P34972 Cannabinoid CB2 receptor 80.87% 97.25%
CHEMBL3902 P09211 Glutathione S-transferase Pi 80.19% 93.81%

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.
Rosa transmorrisonensis

Cross-Links

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PubChem 28343937
NPASS NPC202808