Terremide A

Details

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Internal ID 739f6894-9713-4385-b499-f2e70ab79353
Taxonomy Benzenoids > Benzene and substituted derivatives > Anilides > Aromatic anilides > Benzanilides
IUPAC Name methyl 3-hydroxy-2-[[2-(pyridine-3-carbonylamino)benzoyl]amino]benzoate
SMILES (Canonical) COC(=O)C1=C(C(=CC=C1)O)NC(=O)C2=CC=CC=C2NC(=O)C3=CN=CC=C3
SMILES (Isomeric) COC(=O)C1=C(C(=CC=C1)O)NC(=O)C2=CC=CC=C2NC(=O)C3=CN=CC=C3
InChI InChI=1S/C21H17N3O5/c1-29-21(28)15-8-4-10-17(25)18(15)24-20(27)14-7-2-3-9-16(14)23-19(26)13-6-5-11-22-12-13/h2-12,25H,1H3,(H,23,26)(H,24,27)
InChI Key HGILROHNRVPEBC-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C21H17N3O5
Molecular Weight 391.40 g/mol
Exact Mass 391.11682065 g/mol
Topological Polar Surface Area (TPSA) 118.00 Ų
XlogP 3.10
Atomic LogP (AlogP) 3.08
H-Bond Acceptor 6
H-Bond Donor 3
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Terremide A

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.6561 65.61%
Caco-2 - 0.8264 82.64%
Blood Brain Barrier - 0.7000 70.00%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Mitochondria 0.6924 69.24%
OATP2B1 inhibitior - 0.8480 84.80%
OATP1B1 inhibitior + 0.9270 92.70%
OATP1B3 inhibitior + 0.9475 94.75%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior + 0.6538 65.38%
P-glycoprotein inhibitior - 0.6356 63.56%
P-glycoprotein substrate - 0.5227 52.27%
CYP3A4 substrate - 0.5000 50.00%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8953 89.53%
CYP3A4 inhibition - 0.7774 77.74%
CYP2C9 inhibition - 0.7177 71.77%
CYP2C19 inhibition - 0.8753 87.53%
CYP2D6 inhibition - 0.9591 95.91%
CYP1A2 inhibition + 0.6086 60.86%
CYP2C8 inhibition + 0.8963 89.63%
CYP inhibitory promiscuity - 0.7379 73.79%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.8744 87.44%
Carcinogenicity (trinary) Non-required 0.6752 67.52%
Eye corrosion - 0.9953 99.53%
Eye irritation - 0.9511 95.11%
Skin irritation - 0.8858 88.58%
Skin corrosion - 0.9725 97.25%
Ames mutagenesis - 0.5600 56.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4111 41.11%
Micronuclear + 0.9000 90.00%
Hepatotoxicity - 0.5163 51.63%
skin sensitisation - 0.9477 94.77%
Respiratory toxicity + 0.6444 64.44%
Reproductive toxicity + 0.7444 74.44%
Mitochondrial toxicity + 0.5875 58.75%
Nephrotoxicity + 0.5802 58.02%
Acute Oral Toxicity (c) III 0.6271 62.71%
Estrogen receptor binding + 0.5533 55.33%
Androgen receptor binding + 0.5871 58.71%
Thyroid receptor binding - 0.6262 62.62%
Glucocorticoid receptor binding + 0.6221 62.21%
Aromatase binding - 0.6450 64.50%
PPAR gamma + 0.6981 69.81%
Honey bee toxicity - 0.9210 92.10%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.6100 61.00%
Fish aquatic toxicity + 0.6606 66.06%

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
CHEMBL2535 P11166 Glucose transporter 96.94% 98.75%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 96.15% 81.11%
CHEMBL3714130 P46095 G-protein coupled receptor 6 95.60% 97.36%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 94.36% 99.23%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 93.30% 89.34%
CHEMBL1293294 P51151 Ras-related protein Rab-9A 92.78% 87.67%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.90% 96.09%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 91.86% 91.07%
CHEMBL3401 O75469 Pregnane X receptor 90.73% 94.73%
CHEMBL1951 P21397 Monoamine oxidase A 90.11% 91.49%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 87.26% 94.00%
CHEMBL2095172 P14867 GABA-A receptor; alpha-1/beta-2/gamma-2 86.77% 92.67%
CHEMBL4179 P45984 c-Jun N-terminal kinase 2 86.73% 90.75%
CHEMBL221 P23219 Cyclooxygenase-1 86.68% 90.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.62% 86.33%
CHEMBL2094127 P06493 Cyclin-dependent kinase 1/cyclin B 85.51% 96.00%
CHEMBL2581 P07339 Cathepsin D 85.15% 98.95%
CHEMBL2096618 P11274 Bcr/Abl fusion protein 84.86% 85.83%
CHEMBL1255126 O15151 Protein Mdm4 83.37% 90.20%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 82.32% 95.50%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 82.01% 93.03%
CHEMBL1868 P17948 Vascular endothelial growth factor receptor 1 81.81% 96.47%
CHEMBL4901 P54753 Ephrin type-B receptor 3 81.43% 87.50%
CHEMBL2041 P07949 Tyrosine-protein kinase receptor RET 81.12% 91.79%

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.
Phaseolus lunatus

Cross-Links

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PubChem 139585987
LOTUS LTS0011498
wikiData Q105289644