Tryptoquivaline K

Details

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Internal ID f688768f-1232-4a9d-9148-c7df58d41b0d
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Amino acids, peptides, and analogues > Alpha amino acids and derivatives > Alpha amino acid esters
IUPAC Name
SMILES (Canonical) CC(=O)N1C2C3(CC(C(=O)O3)N4C=NC5=CC=CC=C5C4=O)C6=CC=CC=C6N2C(=O)C17CC7
SMILES (Isomeric) CC(=O)N1[C@@H]2[C@@]3(C[C@H](C(=O)O3)N4C=NC5=CC=CC=C5C4=O)C6=CC=CC=C6N2C(=O)C17CC7
InChI InChI=1S/C25H20N4O5/c1-14(30)29-22-25(16-7-3-5-9-18(16)28(22)23(33)24(29)10-11-24)12-19(21(32)34-25)27-13-26-17-8-4-2-6-15(17)20(27)31/h2-9,13,19,22H,10-12H2,1H3/t19-,22-,25-/m1/s1
InChI Key XCCSYLWRYYKLSU-OPJGWUQDSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C25H20N4O5
Molecular Weight 456.40 g/mol
Exact Mass 456.14336975 g/mol
Topological Polar Surface Area (TPSA) 99.60 Ų
XlogP 1.30
Atomic LogP (AlogP) 1.85
H-Bond Acceptor 7
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Tryptoquivaline K

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9728 97.28%
Caco-2 - 0.7960 79.60%
Blood Brain Barrier + 0.8250 82.50%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Mitochondria 0.5683 56.83%
OATP2B1 inhibitior - 0.8595 85.95%
OATP1B1 inhibitior + 0.8909 89.09%
OATP1B3 inhibitior + 0.9391 93.91%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.8316 83.16%
BSEP inhibitior + 0.9909 99.09%
P-glycoprotein inhibitior + 0.8673 86.73%
P-glycoprotein substrate + 0.5874 58.74%
CYP3A4 substrate + 0.6806 68.06%
CYP2C9 substrate - 0.5906 59.06%
CYP2D6 substrate - 0.8671 86.71%
CYP3A4 inhibition - 0.5557 55.57%
CYP2C9 inhibition + 0.6013 60.13%
CYP2C19 inhibition + 0.5169 51.69%
CYP2D6 inhibition - 0.8330 83.30%
CYP1A2 inhibition - 0.5500 55.00%
CYP2C8 inhibition + 0.5903 59.03%
CYP inhibitory promiscuity - 0.6051 60.51%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8000 80.00%
Carcinogenicity (trinary) Non-required 0.5344 53.44%
Eye corrosion - 0.9883 98.83%
Eye irritation - 0.9633 96.33%
Skin irritation - 0.8145 81.45%
Skin corrosion - 0.9433 94.33%
Ames mutagenesis - 0.6200 62.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6550 65.50%
Micronuclear + 0.8600 86.00%
Hepatotoxicity + 0.6375 63.75%
skin sensitisation - 0.8781 87.81%
Respiratory toxicity + 0.8333 83.33%
Reproductive toxicity + 0.7444 74.44%
Mitochondrial toxicity + 0.8875 88.75%
Nephrotoxicity + 0.5588 55.88%
Acute Oral Toxicity (c) III 0.5215 52.15%
Estrogen receptor binding + 0.7689 76.89%
Androgen receptor binding + 0.7599 75.99%
Thyroid receptor binding + 0.6782 67.82%
Glucocorticoid receptor binding + 0.7201 72.01%
Aromatase binding + 0.5418 54.18%
PPAR gamma + 0.7026 70.26%
Honey bee toxicity - 0.8253 82.53%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.5300 53.00%
Fish aquatic toxicity + 0.7937 79.37%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.97% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.34% 91.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 97.20% 85.14%
CHEMBL1806 P11388 DNA topoisomerase II alpha 95.71% 89.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 94.53% 99.23%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.70% 95.56%
CHEMBL2581 P07339 Cathepsin D 92.83% 98.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 91.00% 94.45%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 88.72% 94.00%
CHEMBL2140 P48775 Tryptophan 2,3-dioxygenase 87.37% 98.46%
CHEMBL1937 Q92769 Histone deacetylase 2 86.82% 94.75%
CHEMBL2095226 P05556 Integrin alpha-5/beta-1 86.58% 96.39%
CHEMBL2535 P11166 Glucose transporter 85.50% 98.75%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.06% 86.33%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 81.97% 93.65%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 81.90% 94.62%
CHEMBL3192 Q9BY41 Histone deacetylase 8 80.44% 93.99%

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 71604970
LOTUS LTS0156166
wikiData Q77506048