Tryptoquialanine B

Details

Top
Internal ID 0011d167-b0c4-4fd2-b6eb-a4d249092c05
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 [(1S)-1-[3-[(2S,3'R,3aS,4S)-3-hydroxy-2-methyl-1,2'-dioxospiro[2,3a-dihydroimidazo[1,2-a]indole-4,5'-oxolane]-3'-yl]-4-oxoquinazolin-2-yl]ethyl] acetate
SMILES (Canonical) CC1C(=O)N2C(N1O)C3(CC(C(=O)O3)N4C(=O)C5=CC=CC=C5N=C4C(C)OC(=O)C)C6=CC=CC=C62
SMILES (Isomeric) C[C@H]1C(=O)N2[C@@H](N1O)[C@]3(C[C@H](C(=O)O3)N4C(=O)C5=CC=CC=C5N=C4[C@H](C)OC(=O)C)C6=CC=CC=C62
InChI InChI=1S/C26H24N4O7/c1-13-22(32)29-19-11-7-5-9-17(19)26(25(29)30(13)35)12-20(24(34)37-26)28-21(14(2)36-15(3)31)27-18-10-6-4-8-16(18)23(28)33/h4-11,13-14,20,25,35H,12H2,1-3H3/t13-,14-,20+,25-,26-/m0/s1
InChI Key UNRJSEBGHKFHQK-NHYRABQJSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

Top
Molecular Formula C26H24N4O7
Molecular Weight 504.50 g/mol
Exact Mass 504.16449912 g/mol
Topological Polar Surface Area (TPSA) 129.00 Ų
XlogP 1.70
Atomic LogP (AlogP) 2.17
H-Bond Acceptor 10
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of Tryptoquialanine B

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8944 89.44%
Caco-2 - 0.7118 71.18%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability - 0.6857 68.57%
Subcellular localzation Mitochondria 0.4174 41.74%
OATP2B1 inhibitior - 0.8592 85.92%
OATP1B1 inhibitior + 0.8793 87.93%
OATP1B3 inhibitior + 0.9339 93.39%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior + 0.9532 95.32%
P-glycoprotein inhibitior + 0.8693 86.93%
P-glycoprotein substrate - 0.5160 51.60%
CYP3A4 substrate + 0.7074 70.74%
CYP2C9 substrate - 0.7878 78.78%
CYP2D6 substrate - 0.8784 87.84%
CYP3A4 inhibition - 0.5283 52.83%
CYP2C9 inhibition - 0.5425 54.25%
CYP2C19 inhibition - 0.6567 65.67%
CYP2D6 inhibition - 0.8919 89.19%
CYP1A2 inhibition - 0.7967 79.67%
CYP2C8 inhibition + 0.5413 54.13%
CYP inhibitory promiscuity - 0.5587 55.87%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.7400 74.00%
Carcinogenicity (trinary) Non-required 0.4793 47.93%
Eye corrosion - 0.9845 98.45%
Eye irritation - 0.9381 93.81%
Skin irritation - 0.7903 79.03%
Skin corrosion - 0.9388 93.88%
Ames mutagenesis - 0.5300 53.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4788 47.88%
Micronuclear + 0.8700 87.00%
Hepatotoxicity + 0.7698 76.98%
skin sensitisation - 0.8712 87.12%
Respiratory toxicity + 0.8111 81.11%
Reproductive toxicity + 0.8000 80.00%
Mitochondrial toxicity + 0.8375 83.75%
Nephrotoxicity + 0.7843 78.43%
Acute Oral Toxicity (c) III 0.5987 59.87%
Estrogen receptor binding + 0.7329 73.29%
Androgen receptor binding + 0.7619 76.19%
Thyroid receptor binding + 0.6498 64.98%
Glucocorticoid receptor binding + 0.8315 83.15%
Aromatase binding + 0.5437 54.37%
PPAR gamma + 0.7173 71.73%
Honey bee toxicity - 0.7823 78.23%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.5000 50.00%
Fish aquatic toxicity + 0.8768 87.68%

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
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 98.67% 85.14%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.45% 96.09%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 94.82% 99.23%
CHEMBL2581 P07339 Cathepsin D 94.75% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.69% 91.11%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 94.30% 94.62%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.10% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.55% 86.33%
CHEMBL1806 P11388 DNA topoisomerase II alpha 89.46% 89.00%
CHEMBL1821 P08173 Muscarinic acetylcholine receptor M4 85.86% 94.08%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 84.86% 100.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 83.11% 94.00%
CHEMBL216 P11229 Muscarinic acetylcholine receptor M1 83.06% 94.23%

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.
There are no matching plants.

Cross-Links

Top
PubChem 11049404
LOTUS LTS0257593
wikiData Q75064842