Terremide C

Details

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Internal ID 40079a11-e7e8-4775-8284-3ca4839c1693
Taxonomy Organoheterocyclic compounds > Diazines > Pyrimidines and pyrimidine derivatives > Pyridinylpyrimidines
IUPAC Name methyl 3,4,5-trimethoxy-2-(4-oxo-2-pyridin-3-ylquinazolin-3-yl)benzoate
SMILES (Canonical) COC1=C(C(=C(C(=C1)C(=O)OC)N2C(=NC3=CC=CC=C3C2=O)C4=CN=CC=C4)OC)OC
SMILES (Isomeric) COC1=C(C(=C(C(=C1)C(=O)OC)N2C(=NC3=CC=CC=C3C2=O)C4=CN=CC=C4)OC)OC
InChI InChI=1S/C24H21N3O6/c1-30-18-12-16(24(29)33-4)19(21(32-3)20(18)31-2)27-22(14-8-7-11-25-13-14)26-17-10-6-5-9-15(17)23(27)28/h5-13H,1-4H3
InChI Key AVVXZSFAPUSQEX-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C24H21N3O6
Molecular Weight 447.40 g/mol
Exact Mass 447.14303540 g/mol
Topological Polar Surface Area (TPSA) 99.60 Ų
XlogP 2.80
Atomic LogP (AlogP) 3.26
H-Bond Acceptor 9
H-Bond Donor 0
Rotatable Bonds 6

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Terremide C

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9082 90.82%
Caco-2 + 0.7431 74.31%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability + 0.6714 67.14%
Subcellular localzation Mitochondria 0.5446 54.46%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9201 92.01%
OATP1B3 inhibitior + 0.9372 93.72%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior + 0.7087 70.87%
P-glycoprotein inhibitior + 0.8462 84.62%
P-glycoprotein substrate - 0.6531 65.31%
CYP3A4 substrate + 0.6022 60.22%
CYP2C9 substrate + 0.5764 57.64%
CYP2D6 substrate - 0.8542 85.42%
CYP3A4 inhibition - 0.7888 78.88%
CYP2C9 inhibition + 0.5430 54.30%
CYP2C19 inhibition - 0.8546 85.46%
CYP2D6 inhibition - 0.9670 96.70%
CYP1A2 inhibition - 0.8445 84.45%
CYP2C8 inhibition + 0.9241 92.41%
CYP inhibitory promiscuity - 0.7613 76.13%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8600 86.00%
Carcinogenicity (trinary) Non-required 0.5076 50.76%
Eye corrosion - 0.9911 99.11%
Eye irritation - 0.8459 84.59%
Skin irritation - 0.8252 82.52%
Skin corrosion - 0.9620 96.20%
Ames mutagenesis + 0.6600 66.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6947 69.47%
Micronuclear + 0.8700 87.00%
Hepatotoxicity + 0.6691 66.91%
skin sensitisation - 0.9371 93.71%
Respiratory toxicity + 0.7778 77.78%
Reproductive toxicity + 0.6889 68.89%
Mitochondrial toxicity + 0.8125 81.25%
Nephrotoxicity - 0.7610 76.10%
Acute Oral Toxicity (c) III 0.5750 57.50%
Estrogen receptor binding + 0.8751 87.51%
Androgen receptor binding + 0.5363 53.63%
Thyroid receptor binding + 0.7858 78.58%
Glucocorticoid receptor binding + 0.7532 75.32%
Aromatase binding - 0.5768 57.68%
PPAR gamma + 0.7441 74.41%
Honey bee toxicity - 0.8883 88.83%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.6700 67.00%
Fish aquatic toxicity + 0.7484 74.84%

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
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 99.59% 85.14%
CHEMBL1293249 Q13887 Kruppel-like factor 5 97.15% 86.33%
CHEMBL2581 P07339 Cathepsin D 95.92% 98.95%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 94.92% 99.23%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 94.87% 95.50%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 94.51% 94.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.56% 96.09%
CHEMBL1868 P17948 Vascular endothelial growth factor receptor 1 93.54% 96.47%
CHEMBL2535 P11166 Glucose transporter 92.06% 98.75%
CHEMBL3714130 P46095 G-protein coupled receptor 6 89.92% 97.36%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 88.78% 91.11%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 88.70% 99.15%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 88.09% 81.11%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.94% 99.17%
CHEMBL2094127 P06493 Cyclin-dependent kinase 1/cyclin B 87.66% 96.00%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 87.24% 94.42%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.79% 95.56%
CHEMBL2095172 P14867 GABA-A receptor; alpha-1/beta-2/gamma-2 86.24% 92.67%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 86.12% 96.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 85.42% 89.00%
CHEMBL1741221 Q9Y4P1 Cysteine protease ATG4B 84.64% 87.50%
CHEMBL4208 P20618 Proteasome component C5 82.85% 90.00%
CHEMBL3976 Q9UHL4 Dipeptidyl peptidase II 81.96% 92.29%
CHEMBL1255126 O15151 Protein Mdm4 81.48% 90.20%

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 71726178
LOTUS LTS0197956
wikiData Q77310224