Helietidine

Details

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Internal ID 832a1224-11cc-4307-ba7d-026efa475bac
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Chromenopyridines
IUPAC Name 2,2-dimethyl-7-(2-methylbut-3-en-2-yl)-9H-pyrano[3,2-g]quinolin-8-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C19H21NO2/c1-6-18(2,3)14-10-13-9-12-7-8-19(4,5)22-16(12)11-15(13)20-17(14)21/h6-11H,1H2,2-5H3,(H,20,21)
InChI Key XAZRWJYBHVVNMC-UHFFFAOYSA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C19H21NO2
Molecular Weight 295.40 g/mol
Exact Mass 295.157228913 g/mol
Topological Polar Surface Area (TPSA) 38.30 Ų
XlogP 4.20
Atomic LogP (AlogP) 4.18
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Helietidine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9975 99.75%
Caco-2 + 0.6114 61.14%
Blood Brain Barrier + 0.8629 86.29%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Mitochondria 0.6300 63.00%
OATP2B1 inhibitior - 0.8571 85.71%
OATP1B1 inhibitior + 0.9121 91.21%
OATP1B3 inhibitior + 0.9622 96.22%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior + 0.8432 84.32%
P-glycoprotein inhibitior - 0.6197 61.97%
P-glycoprotein substrate - 0.7813 78.13%
CYP3A4 substrate + 0.5529 55.29%
CYP2C9 substrate - 0.8000 80.00%
CYP2D6 substrate - 0.8556 85.56%
CYP3A4 inhibition - 0.7263 72.63%
CYP2C9 inhibition + 0.5161 51.61%
CYP2C19 inhibition + 0.6554 65.54%
CYP2D6 inhibition - 0.9216 92.16%
CYP1A2 inhibition + 0.8529 85.29%
CYP2C8 inhibition - 0.6382 63.82%
CYP inhibitory promiscuity + 0.5261 52.61%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9200 92.00%
Carcinogenicity (trinary) Non-required 0.5017 50.17%
Eye corrosion - 0.9906 99.06%
Eye irritation + 0.7629 76.29%
Skin irritation - 0.8179 81.79%
Skin corrosion - 0.9543 95.43%
Ames mutagenesis + 0.5600 56.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7590 75.90%
Micronuclear + 0.6200 62.00%
Hepatotoxicity + 0.5551 55.51%
skin sensitisation - 0.6897 68.97%
Respiratory toxicity + 0.6222 62.22%
Reproductive toxicity + 0.6333 63.33%
Mitochondrial toxicity - 0.5125 51.25%
Nephrotoxicity + 0.6766 67.66%
Acute Oral Toxicity (c) III 0.5984 59.84%
Estrogen receptor binding + 0.9722 97.22%
Androgen receptor binding - 0.5749 57.49%
Thyroid receptor binding + 0.8732 87.32%
Glucocorticoid receptor binding + 0.6704 67.04%
Aromatase binding + 0.9261 92.61%
PPAR gamma + 0.6304 63.04%
Honey bee toxicity - 0.8800 88.00%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity + 0.5400 54.00%
Fish aquatic toxicity + 0.8951 89.51%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.63% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 92.66% 94.45%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 92.16% 85.30%
CHEMBL3401 O75469 Pregnane X receptor 91.42% 94.73%
CHEMBL2581 P07339 Cathepsin D 91.24% 98.95%
CHEMBL230 P35354 Cyclooxygenase-2 91.06% 89.63%
CHEMBL253 P34972 Cannabinoid CB2 receptor 90.44% 97.25%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 89.80% 85.14%
CHEMBL4225 P49760 Dual specificity protein kinase CLK2 88.67% 80.96%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.26% 95.56%
CHEMBL1937 Q92769 Histone deacetylase 2 87.58% 94.75%
CHEMBL4051 P13569 Cystic fibrosis transmembrane conductance regulator 86.79% 95.71%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 86.66% 96.77%
CHEMBL2964 P36507 Dual specificity mitogen-activated protein kinase kinase 2 86.56% 80.00%
CHEMBL2708 Q16584 Mitogen-activated protein kinase kinase kinase 11 85.23% 81.14%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.59% 86.33%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 84.00% 99.23%
CHEMBL325 Q13547 Histone deacetylase 1 82.73% 95.92%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 82.58% 93.40%
CHEMBL1806 P11388 DNA topoisomerase II alpha 82.37% 89.00%
CHEMBL4208 P20618 Proteasome component C5 82.14% 90.00%
CHEMBL3310 Q96DB2 Histone deacetylase 11 81.11% 88.56%
CHEMBL4530 P00488 Coagulation factor XIII 80.88% 96.00%
CHEMBL241 Q14432 Phosphodiesterase 3A 80.76% 92.94%
CHEMBL4829 O00763 Acetyl-CoA carboxylase 2 80.13% 98.00%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 80.11% 91.07%

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.
Helietta apiculata

Cross-Links

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PubChem 134830748
LOTUS LTS0116586
wikiData Q105324260