(111C)methyl 2-hydroxybenzoate

Details

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Internal ID c71c1ae0-1a8a-43c2-9fad-cb9c9dc90520
Taxonomy Benzenoids > Benzene and substituted derivatives > Benzoic acids and derivatives > Benzoic acid esters > o-Hydroxybenzoic acid esters
IUPAC Name (111C)methyl 2-hydroxybenzoate
SMILES (Canonical) COC(=O)C1=CC=CC=C1O
SMILES (Isomeric) [11CH3]OC(=O)C1=CC=CC=C1O
InChI InChI=1S/C8H8O3/c1-11-8(10)6-4-2-3-5-7(6)9/h2-5,9H,1H3/i1-1
InChI Key OSWPMRLSEDHDFF-BJUDXGSMSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C8H8O3
Molecular Weight 151.15 g/mol
Exact Mass 151.0587767 g/mol
Topological Polar Surface Area (TPSA) 46.50 Ų
XlogP 2.30
Atomic LogP (AlogP) 1.18
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (111C)methyl 2-hydroxybenzoate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9959 99.59%
Caco-2 + 0.6465 64.65%
Blood Brain Barrier - 0.6250 62.50%
Human oral bioavailability + 0.8143 81.43%
Subcellular localzation Mitochondria 0.9381 93.81%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9539 95.39%
OATP1B3 inhibitior + 0.9905 99.05%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9480 94.80%
P-glycoprotein inhibitior - 0.9842 98.42%
P-glycoprotein substrate - 0.9821 98.21%
CYP3A4 substrate - 0.6558 65.58%
CYP2C9 substrate - 0.6371 63.71%
CYP2D6 substrate - 0.8610 86.10%
CYP3A4 inhibition - 0.9780 97.80%
CYP2C9 inhibition - 0.9759 97.59%
CYP2C19 inhibition - 0.8628 86.28%
CYP2D6 inhibition - 0.9781 97.81%
CYP1A2 inhibition - 0.8013 80.13%
CYP2C8 inhibition - 0.7509 75.09%
CYP inhibitory promiscuity - 0.9199 91.99%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.6170 61.70%
Carcinogenicity (trinary) Non-required 0.6455 64.55%
Eye corrosion + 0.8625 86.25%
Eye irritation + 1.0000 100.00%
Skin irritation + 0.9040 90.40%
Skin corrosion - 0.9395 93.95%
Ames mutagenesis - 0.9200 92.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8472 84.72%
Micronuclear + 0.5737 57.37%
Hepatotoxicity - 0.7625 76.25%
skin sensitisation - 0.8845 88.45%
Respiratory toxicity - 0.9889 98.89%
Reproductive toxicity + 0.8667 86.67%
Mitochondrial toxicity - 0.9625 96.25%
Nephrotoxicity + 0.6398 63.98%
Acute Oral Toxicity (c) III 0.8105 81.05%
Estrogen receptor binding - 0.9117 91.17%
Androgen receptor binding - 0.8328 83.28%
Thyroid receptor binding - 0.7781 77.81%
Glucocorticoid receptor binding - 0.9413 94.13%
Aromatase binding - 0.8746 87.46%
PPAR gamma - 0.8153 81.53%
Honey bee toxicity - 0.9746 97.46%
Biodegradation + 0.9250 92.50%
Crustacea aquatic toxicity - 0.8400 84.00%
Fish aquatic toxicity + 0.8788 87.88%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
CHEMBL1293235 P02545 Prelamin-A/C 794.3 nM
Potency
via Super-PRED

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.53% 91.11%
CHEMBL2581 P07339 Cathepsin D 90.86% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.11% 96.09%
CHEMBL2535 P11166 Glucose transporter 85.00% 98.75%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 84.62% 95.50%
CHEMBL4208 P20618 Proteasome component C5 84.41% 90.00%
CHEMBL3401 O75469 Pregnane X receptor 84.08% 94.73%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.21% 95.56%

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.
Ardisia japonica
Camptotheca acuminata
Eleutherococcus nodiflorus
Ixora chinensis
Morus alba
Murraya paniculata
Nerium oleander
Prunus mume
Syzygium aromaticum
Uncaria macrophylla

Cross-Links

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PubChem 11378589
NPASS NPC9794