3-Amino-2,3-dihydrobenzoic acid

Details

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Internal ID 0bd14369-fb23-43a5-8d60-3d2a6083a36d
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Amino acids, peptides, and analogues > Amino acids and derivatives > Gamma amino acids and derivatives
IUPAC Name 5-aminocyclohexa-1,3-diene-1-carboxylic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C7H9NO2/c8-6-3-1-2-5(4-6)7(9)10/h1-3,6H,4,8H2,(H,9,10)
InChI Key KFNRJXCQEJIBER-UHFFFAOYSA-N
Popularity 178 references in papers

Physical and Chemical Properties

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Molecular Formula C7H9NO2
Molecular Weight 139.15 g/mol
Exact Mass 139.063328530 g/mol
Topological Polar Surface Area (TPSA) 63.30 Ų
XlogP -2.20
Atomic LogP (AlogP) 0.28
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

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3-Amino-2,3-dihydrobenzoic acid
gabaculine
59556-18-2
5-aminocyclohexa-1,3-diene-1-carboxylic acid
GABACULINE, D.L-
5-Amino-1,3-cyclohexadiene-1-carboxylic acid
NSC-329502
3-Amino-4,6-cyclohexadienecarboxylic acid
87980-11-8
1,3-Cyclohexadiene-1-carboxylicacid,5-amino-(9CI)
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 3-Amino-2,3-dihydrobenzoic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9969 99.69%
Caco-2 + 0.6107 61.07%
Blood Brain Barrier + 0.7250 72.50%
Human oral bioavailability + 0.7143 71.43%
Subcellular localzation Lysosomes 0.5869 58.69%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9670 96.70%
OATP1B3 inhibitior + 0.9429 94.29%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.9175 91.75%
P-glycoprotein inhibitior - 0.9922 99.22%
P-glycoprotein substrate - 0.9421 94.21%
CYP3A4 substrate - 0.7477 74.77%
CYP2C9 substrate - 0.7846 78.46%
CYP2D6 substrate - 0.8359 83.59%
CYP3A4 inhibition - 0.9326 93.26%
CYP2C9 inhibition - 0.9154 91.54%
CYP2C19 inhibition - 0.9546 95.46%
CYP2D6 inhibition - 0.9530 95.30%
CYP1A2 inhibition - 0.9318 93.18%
CYP2C8 inhibition - 0.8982 89.82%
CYP inhibitory promiscuity - 0.9682 96.82%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5743 57.43%
Carcinogenicity (trinary) Non-required 0.6760 67.60%
Eye corrosion - 0.9767 97.67%
Eye irritation + 0.8054 80.54%
Skin irritation - 0.5869 58.69%
Skin corrosion - 0.7327 73.27%
Ames mutagenesis - 0.7800 78.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8956 89.56%
Micronuclear + 0.5300 53.00%
Hepatotoxicity + 0.8219 82.19%
skin sensitisation - 0.7995 79.95%
Respiratory toxicity + 0.6556 65.56%
Reproductive toxicity - 0.5222 52.22%
Mitochondrial toxicity - 0.5125 51.25%
Nephrotoxicity - 0.5867 58.67%
Acute Oral Toxicity (c) III 0.6471 64.71%
Estrogen receptor binding - 0.9535 95.35%
Androgen receptor binding - 0.8203 82.03%
Thyroid receptor binding - 0.8328 83.28%
Glucocorticoid receptor binding - 0.8749 87.49%
Aromatase binding - 0.8835 88.35%
PPAR gamma - 0.7609 76.09%
Honey bee toxicity - 0.8527 85.27%
Biodegradation - 0.5500 55.00%
Crustacea aquatic toxicity - 0.7000 70.00%
Fish aquatic toxicity - 0.4723 47.23%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
CHEMBL4040 P28482 MAP kinase ERK2 6.3 nM
Potency
via Super-PRED

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.40% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 87.28% 97.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.74% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 85.66% 91.11%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 82.42% 93.00%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 3445
LOTUS LTS0209757
wikiData Q1007138