Braylin

Details

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Internal ID 7f29bdca-cb29-4e28-b7bb-fd1edf413baf
Taxonomy Phenylpropanoids and polyketides > Coumarins and derivatives > Pyranocoumarins > Angular pyranocoumarins
IUPAC Name 6-methoxy-8,8-dimethylpyrano[2,3-f]chromen-2-one
SMILES (Canonical) CC1(C=CC2=C3C(=CC(=C2O1)OC)C=CC(=O)O3)C
SMILES (Isomeric) CC1(C=CC2=C3C(=CC(=C2O1)OC)C=CC(=O)O3)C
InChI InChI=1S/C15H14O4/c1-15(2)7-6-10-13-9(4-5-12(16)18-13)8-11(17-3)14(10)19-15/h4-8H,1-3H3
InChI Key UOFNVZWWIXXTMZ-UHFFFAOYSA-N
Popularity 17 references in papers

Physical and Chemical Properties

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Molecular Formula C15H14O4
Molecular Weight 258.27 g/mol
Exact Mass 258.08920892 g/mol
Topological Polar Surface Area (TPSA) 44.80 Ų
XlogP 2.80
Atomic LogP (AlogP) 2.99
H-Bond Acceptor 4
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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6054-10-0
6-methoxy-8,8-dimethylpyrano[2,3-f]chromen-2-one
2H, 8H-Benzo[1,2-b
CHEMBL529210
6-Methoxy-8,8-dimethyl-2H,8H-pyrano[2,3-f]chromen-2-one
Brayelin
2H-1-Benzopyran-6-acrylic acid, 5-hydroxy-8-methoxy-2,2-dimethyl-, delta-lactone
UOFNVZWWIXXTMZ-UHFFFAOYSA-N
HY-N2958
BDBM50008737
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Braylin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9857 98.57%
Caco-2 + 0.5857 58.57%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability + 0.7143 71.43%
Subcellular localzation Mitochondria 0.6593 65.93%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9517 95.17%
OATP1B3 inhibitior + 0.9668 96.68%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior + 0.6258 62.58%
P-glycoprotein inhibitior - 0.6650 66.50%
P-glycoprotein substrate - 0.7980 79.80%
CYP3A4 substrate - 0.5191 51.91%
CYP2C9 substrate - 0.6755 67.55%
CYP2D6 substrate - 0.8349 83.49%
CYP3A4 inhibition + 0.6015 60.15%
CYP2C9 inhibition - 0.9240 92.40%
CYP2C19 inhibition + 0.6453 64.53%
CYP2D6 inhibition - 0.6834 68.34%
CYP1A2 inhibition + 0.5685 56.85%
CYP2C8 inhibition + 0.4748 47.48%
CYP inhibitory promiscuity + 0.5673 56.73%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Danger 0.5011 50.11%
Eye corrosion - 0.9744 97.44%
Eye irritation + 0.7586 75.86%
Skin irritation - 0.7913 79.13%
Skin corrosion - 0.9775 97.75%
Ames mutagenesis - 0.5900 59.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6570 65.70%
Micronuclear + 0.5700 57.00%
Hepatotoxicity + 0.6949 69.49%
skin sensitisation - 0.7855 78.55%
Respiratory toxicity - 0.6222 62.22%
Reproductive toxicity + 0.6778 67.78%
Mitochondrial toxicity - 0.6000 60.00%
Nephrotoxicity + 0.5511 55.11%
Acute Oral Toxicity (c) III 0.4429 44.29%
Estrogen receptor binding + 0.9422 94.22%
Androgen receptor binding + 0.6861 68.61%
Thyroid receptor binding + 0.5859 58.59%
Glucocorticoid receptor binding + 0.8320 83.20%
Aromatase binding + 0.8684 86.84%
PPAR gamma + 0.6470 64.70%
Honey bee toxicity - 0.8065 80.65%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.5500 55.00%
Fish aquatic toxicity + 0.9675 96.75%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
CHEMBL288 Q08499 Phosphodiesterase 4D 960 nM
960 nM
IC50
IC50
PMID: 24597921
via Super-PRED

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.67% 91.11%
CHEMBL3192 Q9BY41 Histone deacetylase 8 93.73% 93.99%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 93.34% 94.00%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 91.81% 85.30%
CHEMBL1255126 O15151 Protein Mdm4 88.93% 90.20%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.19% 86.33%
CHEMBL4208 P20618 Proteasome component C5 87.74% 90.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.50% 95.56%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 87.33% 94.45%
CHEMBL1937 Q92769 Histone deacetylase 2 86.39% 94.75%
CHEMBL2581 P07339 Cathepsin D 85.17% 98.95%
CHEMBL1907 P15144 Aminopeptidase N 84.72% 93.31%
CHEMBL2535 P11166 Glucose transporter 81.73% 98.75%
CHEMBL4145 Q9UKV0 Histone deacetylase 9 81.58% 85.49%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 81.47% 100.00%
CHEMBL4306 P22460 Voltage-gated potassium channel subunit Kv1.5 81.40% 94.03%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 80.87% 90.71%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.61% 99.23%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 80.48% 89.62%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 80.10% 92.62%

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.
Boronia pinnata
Bosistoa transversa
Cedrelopsis grevei
Flindersia brayleyana
Geleznowia verrucosa
Menyanthes trifoliata
Metrodorea flavida
Murraya paniculata
Pitavia punctata
Spiranthera odoratissima
Ticorea longiflora
Toddalia asiatica

Cross-Links

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PubChem 618370
NPASS NPC167517
ChEMBL CHEMBL529210
LOTUS LTS0213074
wikiData Q104403416