Carotamine

Details

Top
Internal ID 9facc591-aeaa-49ac-88f0-8e4a77c41dd7
Taxonomy Benzenoids > Benzene and substituted derivatives > Anilides > Aromatic anilides > Benzanilides
IUPAC Name 2-amino-4-[(4-aminobenzoyl)amino]benzoic acid
SMILES (Canonical) C1=CC(=CC=C1C(=O)NC2=CC(=C(C=C2)C(=O)O)N)N
SMILES (Isomeric) C1=CC(=CC=C1C(=O)NC2=CC(=C(C=C2)C(=O)O)N)N
InChI InChI=1S/C14H13N3O3/c15-9-3-1-8(2-4-9)13(18)17-10-5-6-11(14(19)20)12(16)7-10/h1-7H,15-16H2,(H,17,18)(H,19,20)
InChI Key GGUOSFAJMKBDFW-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C14H13N3O3
Molecular Weight 271.27 g/mol
Exact Mass 271.09569129 g/mol
Topological Polar Surface Area (TPSA) 118.00 Ų
XlogP 2.30
Atomic LogP (AlogP) 1.80
H-Bond Acceptor 4
H-Bond Donor 4
Rotatable Bonds 3

Synonyms

Top
CHEBI:191847
2-Amino-4-(4-aminobenzoylamino)benzoic acid
2-amino-4-[(4-aminobenzoyl)amino]benzoic acid

2D Structure

Top
2D Structure of Carotamine

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.6399 63.99%
Caco-2 + 0.5674 56.74%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability + 0.7143 71.43%
Subcellular localzation Mitochondria 0.8166 81.66%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9602 96.02%
OATP1B3 inhibitior + 0.9425 94.25%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.8250 82.50%
P-glycoprotein inhibitior - 0.9387 93.87%
P-glycoprotein substrate - 0.7678 76.78%
CYP3A4 substrate - 0.7412 74.12%
CYP2C9 substrate - 0.7724 77.24%
CYP2D6 substrate - 0.8419 84.19%
CYP3A4 inhibition - 0.8774 87.74%
CYP2C9 inhibition - 0.8279 82.79%
CYP2C19 inhibition - 0.9390 93.90%
CYP2D6 inhibition - 0.9667 96.67%
CYP1A2 inhibition + 0.5442 54.42%
CYP2C8 inhibition - 0.7461 74.61%
CYP inhibitory promiscuity - 0.8978 89.78%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6104 61.04%
Carcinogenicity (trinary) Non-required 0.6934 69.34%
Eye corrosion - 0.9938 99.38%
Eye irritation - 0.6639 66.39%
Skin irritation - 0.8597 85.97%
Skin corrosion - 0.9909 99.09%
Ames mutagenesis - 0.5200 52.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7929 79.29%
Micronuclear + 0.8200 82.00%
Hepatotoxicity + 0.6375 63.75%
skin sensitisation - 0.9302 93.02%
Respiratory toxicity - 0.6889 68.89%
Reproductive toxicity - 0.6000 60.00%
Mitochondrial toxicity + 0.5250 52.50%
Nephrotoxicity + 0.6110 61.10%
Acute Oral Toxicity (c) IV 0.6827 68.27%
Estrogen receptor binding + 0.8335 83.35%
Androgen receptor binding + 0.9062 90.62%
Thyroid receptor binding - 0.5648 56.48%
Glucocorticoid receptor binding + 0.7007 70.07%
Aromatase binding + 0.8019 80.19%
PPAR gamma + 0.8298 82.98%
Honey bee toxicity - 0.9757 97.57%
Biodegradation - 1.0000 100.00%
Crustacea aquatic toxicity - 0.7300 73.00%
Fish aquatic toxicity + 0.9586 95.86%

Targets

Top

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
CHEMBL1293277 O15118 Niemann-Pick C1 protein 99.32% 81.11%
CHEMBL1293294 P51151 Ras-related protein Rab-9A 98.13% 87.67%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 94.03% 94.42%
CHEMBL2409 P34913 Epoxide hydratase 91.75% 94.09%
CHEMBL2093869 P05106 Integrin alpha-IIb/beta-3 91.62% 95.42%
CHEMBL2216739 Q92523 Carnitine O-palmitoyltransferase 1, muscle isoform 90.98% 88.33%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 89.96% 89.34%
CHEMBL1255126 O15151 Protein Mdm4 89.32% 90.20%
CHEMBL1287628 Q9Y5S8 NADPH oxidase 1 87.38% 95.48%
CHEMBL4530 P00488 Coagulation factor XIII 86.64% 96.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.64% 95.56%
CHEMBL2535 P11166 Glucose transporter 86.19% 98.75%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.16% 86.33%
CHEMBL340 P08684 Cytochrome P450 3A4 85.01% 91.19%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 84.41% 90.71%
CHEMBL279 P35968 Vascular endothelial growth factor receptor 2 83.88% 95.52%
CHEMBL3401 O75469 Pregnane X receptor 83.01% 94.73%
CHEMBL4040 P28482 MAP kinase ERK2 82.47% 83.82%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 81.54% 97.21%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.47% 99.17%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 80.22% 100.00%

Plants that contains it

Top
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.
Daucus carota

Cross-Links

Top
PubChem 131752767
LOTUS LTS0082801
wikiData Q105008333