(2S)-2,5,7-trihydroxy-2-icosyl-3H-chromen-4-one

Details

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Internal ID b926bd45-2d03-4420-b701-2f605559c945
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Chromones
IUPAC Name (2S)-2,5,7-trihydroxy-2-icosyl-3H-chromen-4-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C29H48O5/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-29(33)23-26(32)28-25(31)21-24(30)22-27(28)34-29/h21-22,30-31,33H,2-20,23H2,1H3/t29-/m0/s1
InChI Key MIOOAVYFDWMZAD-LJAQVGFWSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C29H48O5
Molecular Weight 476.70 g/mol
Exact Mass 476.35017463 g/mol
Topological Polar Surface Area (TPSA) 87.00 Ų
XlogP 11.00
Atomic LogP (AlogP) 8.18
H-Bond Acceptor 5
H-Bond Donor 3
Rotatable Bonds 19

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (2S)-2,5,7-trihydroxy-2-icosyl-3H-chromen-4-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9469 94.69%
Caco-2 - 0.7215 72.15%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability - 0.7429 74.29%
Subcellular localzation Mitochondria 0.6367 63.67%
OATP2B1 inhibitior - 0.7157 71.57%
OATP1B1 inhibitior + 0.9109 91.09%
OATP1B3 inhibitior + 0.9053 90.53%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.6619 66.19%
P-glycoprotein inhibitior - 0.5342 53.42%
P-glycoprotein substrate - 0.7492 74.92%
CYP3A4 substrate + 0.5331 53.31%
CYP2C9 substrate + 0.5976 59.76%
CYP2D6 substrate - 0.8276 82.76%
CYP3A4 inhibition + 0.6900 69.00%
CYP2C9 inhibition - 0.8896 88.96%
CYP2C19 inhibition - 0.6833 68.33%
CYP2D6 inhibition - 0.8976 89.76%
CYP1A2 inhibition - 0.5921 59.21%
CYP2C8 inhibition - 0.5735 57.35%
CYP inhibitory promiscuity - 0.8548 85.48%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.7045 70.45%
Eye corrosion - 0.9903 99.03%
Eye irritation - 0.5547 55.47%
Skin irritation - 0.6283 62.83%
Skin corrosion - 0.8939 89.39%
Ames mutagenesis - 0.8400 84.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6063 60.63%
Micronuclear - 0.8600 86.00%
Hepatotoxicity - 0.5225 52.25%
skin sensitisation - 0.8266 82.66%
Respiratory toxicity - 0.5222 52.22%
Reproductive toxicity + 0.8921 89.21%
Mitochondrial toxicity + 0.8625 86.25%
Nephrotoxicity + 0.8076 80.76%
Acute Oral Toxicity (c) III 0.5744 57.44%
Estrogen receptor binding + 0.8328 83.28%
Androgen receptor binding + 0.7240 72.40%
Thyroid receptor binding - 0.5000 50.00%
Glucocorticoid receptor binding + 0.5948 59.48%
Aromatase binding + 0.5795 57.95%
PPAR gamma + 0.7207 72.07%
Honey bee toxicity - 0.9635 96.35%
Biodegradation - 0.5250 52.50%
Crustacea aquatic toxicity + 0.8469 84.69%
Fish aquatic toxicity + 0.9780 97.80%

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 99.39% 91.11%
CHEMBL2581 P07339 Cathepsin D 98.37% 98.95%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 94.75% 95.17%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 94.59% 94.45%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.71% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.29% 95.56%
CHEMBL1929 P47989 Xanthine dehydrogenase 88.21% 96.12%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.22% 99.17%
CHEMBL1806 P11388 DNA topoisomerase II alpha 87.20% 89.00%
CHEMBL4208 P20618 Proteasome component C5 87.03% 90.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.77% 86.33%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 84.16% 92.08%
CHEMBL3192 Q9BY41 Histone deacetylase 8 83.95% 93.99%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 83.82% 99.23%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 83.71% 90.71%
CHEMBL299 P17252 Protein kinase C alpha 82.34% 98.03%
CHEMBL2069156 Q14145 Kelch-like ECH-associated protein 1 80.87% 82.38%
CHEMBL3401 O75469 Pregnane X receptor 80.22% 94.73%

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.
Antidesma membranaceum

Cross-Links

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PubChem 162935516
LOTUS LTS0178356
wikiData Q105165135