Anthranilate

Details

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Internal ID fd5f5be3-b5ef-4943-939a-4c77a0811cb4
Taxonomy Benzenoids > Benzene and substituted derivatives > Benzoic acids and derivatives > Aminobenzoic acids and derivatives > Aminobenzoic acids
IUPAC Name 2-aminobenzoate
SMILES (Canonical) C1=CC=C(C(=C1)C(=O)[O-])N
SMILES (Isomeric) C1=CC=C(C(=C1)C(=O)[O-])N
InChI InChI=1S/C7H7NO2/c8-6-4-2-1-3-5(6)7(9)10/h1-4H,8H2,(H,9,10)/p-1
InChI Key RWZYAGGXGHYGMB-UHFFFAOYSA-M
Popularity 736 references in papers

Physical and Chemical Properties

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Molecular Formula C7H6NO2-
Molecular Weight 136.13 g/mol
Exact Mass 136.039853434 g/mol
Topological Polar Surface Area (TPSA) 66.20 Ų
XlogP 1.90
Atomic LogP (AlogP) -0.37
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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o-Aminobenzoate
Anthranic acid
2-azanylbenzoate
9031-59-8
CHEBI:16567
DTXSID80420080
3h78
RWZYAGGXGHYGMB-UHFFFAOYSA-M
c0345
A804127
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Anthranilate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9873 98.73%
Caco-2 + 0.9281 92.81%
Blood Brain Barrier + 0.8750 87.50%
Human oral bioavailability + 0.8429 84.29%
Subcellular localzation Mitochondria 0.6293 62.93%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9813 98.13%
OATP1B3 inhibitior + 0.9626 96.26%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.9492 94.92%
P-glycoprotein inhibitior - 0.9861 98.61%
P-glycoprotein substrate - 0.9782 97.82%
CYP3A4 substrate - 0.8142 81.42%
CYP2C9 substrate - 0.5874 58.74%
CYP2D6 substrate - 0.8505 85.05%
CYP3A4 inhibition - 0.9747 97.47%
CYP2C9 inhibition - 0.7907 79.07%
CYP2C19 inhibition - 0.9075 90.75%
CYP2D6 inhibition - 0.9451 94.51%
CYP1A2 inhibition - 0.5141 51.41%
CYP2C8 inhibition - 0.9649 96.49%
CYP inhibitory promiscuity - 0.9461 94.61%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5462 54.62%
Carcinogenicity (trinary) Non-required 0.7121 71.21%
Eye corrosion - 0.8975 89.75%
Eye irritation + 1.0000 100.00%
Skin irritation + 0.6200 62.00%
Skin corrosion - 0.9748 97.48%
Ames mutagenesis - 0.8000 80.00%
Human Ether-a-go-go-Related Gene inhibition - 0.9217 92.17%
Micronuclear + 0.5100 51.00%
Hepatotoxicity + 0.7875 78.75%
skin sensitisation - 0.8197 81.97%
Respiratory toxicity - 0.7222 72.22%
Reproductive toxicity - 0.6111 61.11%
Mitochondrial toxicity - 0.8750 87.50%
Nephrotoxicity + 0.6324 63.24%
Acute Oral Toxicity (c) III 0.5876 58.76%
Estrogen receptor binding - 0.9519 95.19%
Androgen receptor binding - 0.7187 71.87%
Thyroid receptor binding - 0.7303 73.03%
Glucocorticoid receptor binding - 0.9116 91.16%
Aromatase binding - 0.8799 87.99%
PPAR gamma - 0.5765 57.65%
Honey bee toxicity - 0.9679 96.79%
Biodegradation + 0.7250 72.50%
Crustacea aquatic toxicity - 0.8200 82.00%
Fish aquatic toxicity + 0.8362 83.62%

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 92.64% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.89% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.96% 96.09%
CHEMBL4040 P28482 MAP kinase ERK2 85.09% 83.82%

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.
Thymus quinquecostatus
Thymus vulgaris

Cross-Links

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PubChem 5459842
NPASS NPC165951