5-O-methylsorbifolin

Details

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Internal ID 504c0ebd-f4fe-41d6-ac27-f99ad94d1898
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Pyranochromenes
IUPAC Name 6-[(E)-3-hydroxy-3-methylbut-1-enyl]-5-methoxy-2,8,8-trimethylpyrano[2,3-h]chromen-4-one
SMILES (Canonical) CC1=CC(=O)C2=C(C(=C3C(=C2O1)C=CC(O3)(C)C)C=CC(C)(C)O)OC
SMILES (Isomeric) CC1=CC(=O)C2=C(C(=C3C(=C2O1)C=CC(O3)(C)C)/C=C/C(C)(C)O)OC
InChI InChI=1S/C21H24O5/c1-12-11-15(22)16-18(24-6)13(7-9-20(2,3)23)17-14(19(16)25-12)8-10-21(4,5)26-17/h7-11,23H,1-6H3/b9-7+
InChI Key ZFGXXFPHCVSNOP-VQHVLOKHSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C21H24O5
Molecular Weight 356.40 g/mol
Exact Mass 356.16237386 g/mol
Topological Polar Surface Area (TPSA) 65.00 Ų
XlogP 3.20
Atomic LogP (AlogP) 4.08
H-Bond Acceptor 5
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 5-O-methylsorbifolin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9888 98.88%
Caco-2 + 0.5347 53.47%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Mitochondria 0.7710 77.10%
OATP2B1 inhibitior - 0.8627 86.27%
OATP1B1 inhibitior + 0.8947 89.47%
OATP1B3 inhibitior + 0.9870 98.70%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior + 0.7530 75.30%
P-glycoprotein inhibitior - 0.4807 48.07%
P-glycoprotein substrate - 0.7138 71.38%
CYP3A4 substrate + 0.6381 63.81%
CYP2C9 substrate - 0.8166 81.66%
CYP2D6 substrate - 0.8360 83.60%
CYP3A4 inhibition + 0.6948 69.48%
CYP2C9 inhibition - 0.8144 81.44%
CYP2C19 inhibition + 0.7249 72.49%
CYP2D6 inhibition - 0.7361 73.61%
CYP1A2 inhibition + 0.7072 70.72%
CYP2C8 inhibition + 0.5055 50.55%
CYP inhibitory promiscuity + 0.5706 57.06%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9513 95.13%
Carcinogenicity (trinary) Danger 0.5029 50.29%
Eye corrosion - 0.9842 98.42%
Eye irritation + 0.5735 57.35%
Skin irritation - 0.7593 75.93%
Skin corrosion - 0.9729 97.29%
Ames mutagenesis + 0.5936 59.36%
Human Ether-a-go-go-Related Gene inhibition + 0.7152 71.52%
Micronuclear + 0.6200 62.00%
Hepatotoxicity - 0.6143 61.43%
skin sensitisation - 0.8550 85.50%
Respiratory toxicity - 0.5444 54.44%
Reproductive toxicity + 0.7000 70.00%
Mitochondrial toxicity - 0.5875 58.75%
Nephrotoxicity - 0.6530 65.30%
Acute Oral Toxicity (c) III 0.5103 51.03%
Estrogen receptor binding + 0.9145 91.45%
Androgen receptor binding + 0.6096 60.96%
Thyroid receptor binding + 0.6907 69.07%
Glucocorticoid receptor binding + 0.7683 76.83%
Aromatase binding + 0.8507 85.07%
PPAR gamma + 0.8911 89.11%
Honey bee toxicity - 0.7235 72.35%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.5300 53.00%
Fish aquatic toxicity + 0.9635 96.35%

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 97.40% 91.11%
CHEMBL3401 O75469 Pregnane X receptor 96.37% 94.73%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.00% 95.56%
CHEMBL1806 P11388 DNA topoisomerase II alpha 92.68% 89.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 90.80% 94.45%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.76% 86.33%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 87.37% 94.00%
CHEMBL1937 Q92769 Histone deacetylase 2 87.29% 94.75%
CHEMBL2581 P07339 Cathepsin D 86.93% 98.95%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 85.26% 97.14%
CHEMBL4051 P13569 Cystic fibrosis transmembrane conductance regulator 84.03% 95.71%
CHEMBL4829 O00763 Acetyl-CoA carboxylase 2 83.39% 98.00%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 83.07% 91.07%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 82.97% 100.00%
CHEMBL4581 P52732 Kinesin-like protein 1 81.90% 93.18%
CHEMBL2964 P36507 Dual specificity mitogen-activated protein kinase kinase 2 81.76% 80.00%

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.
Spathelia simplex

Cross-Links

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PubChem 13887366
LOTUS LTS0038074
wikiData Q105374149