Castillene D

Details

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Internal ID c0cdcac0-10eb-4a52-af1b-ba3d1e510770
Taxonomy Phenylpropanoids and polyketides > Aurone flavonoids
IUPAC Name 2-(1,3-benzodioxol-5-ylmethyl)-2-methoxyfuro[2,3-e][1]benzofuran-3-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C19H14O6/c1-21-19(9-11-2-4-15-16(8-11)24-10-23-15)18(20)13-3-5-14-12(6-7-22-14)17(13)25-19/h2-8H,9-10H2,1H3
InChI Key HNGNYODKSMNHQW-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C19H14O6
Molecular Weight 338.30 g/mol
Exact Mass 338.07903816 g/mol
Topological Polar Surface Area (TPSA) 67.10 Ų
XlogP 3.50
Atomic LogP (AlogP) 3.32
H-Bond Acceptor 6
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

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126585-63-5
(+)-Castillene D
DTXSID80925601
LMPK12130064
2-[(2H-1,3-Benzodioxol-5-yl)methyl]-2-methoxybenzo[1,2-b:3,4-b']difuran-3(2H)-one

2D Structure

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2D Structure of Castillene D

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9905 99.05%
Caco-2 + 0.6497 64.97%
Blood Brain Barrier + 0.5500 55.00%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.7179 71.79%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9009 90.09%
OATP1B3 inhibitior + 0.9697 96.97%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior + 0.8065 80.65%
P-glycoprotein inhibitior - 0.4697 46.97%
P-glycoprotein substrate - 0.6515 65.15%
CYP3A4 substrate + 0.5985 59.85%
CYP2C9 substrate - 0.8086 80.86%
CYP2D6 substrate - 0.7677 76.77%
CYP3A4 inhibition + 0.8146 81.46%
CYP2C9 inhibition + 0.6606 66.06%
CYP2C19 inhibition + 0.8441 84.41%
CYP2D6 inhibition + 0.5074 50.74%
CYP1A2 inhibition - 0.6265 62.65%
CYP2C8 inhibition + 0.4743 47.43%
CYP inhibitory promiscuity + 0.8152 81.52%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Non-required 0.4207 42.07%
Eye corrosion - 0.9761 97.61%
Eye irritation - 0.8644 86.44%
Skin irritation - 0.7402 74.02%
Skin corrosion - 0.9583 95.83%
Ames mutagenesis - 0.5900 59.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3698 36.98%
Micronuclear + 0.5692 56.92%
Hepatotoxicity + 0.6250 62.50%
skin sensitisation - 0.6198 61.98%
Respiratory toxicity + 0.6444 64.44%
Reproductive toxicity + 0.7556 75.56%
Mitochondrial toxicity - 0.5375 53.75%
Nephrotoxicity - 0.6504 65.04%
Acute Oral Toxicity (c) III 0.6898 68.98%
Estrogen receptor binding + 0.9391 93.91%
Androgen receptor binding + 0.8318 83.18%
Thyroid receptor binding - 0.5410 54.10%
Glucocorticoid receptor binding + 0.7914 79.14%
Aromatase binding + 0.7364 73.64%
PPAR gamma + 0.7231 72.31%
Honey bee toxicity - 0.6989 69.89%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity + 0.5700 57.00%
Fish aquatic toxicity + 0.9562 95.62%

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
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 99.03% 96.77%
CHEMBL2581 P07339 Cathepsin D 98.96% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 98.48% 91.11%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 95.25% 94.80%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 94.48% 94.45%
CHEMBL1951 P21397 Monoamine oxidase A 93.46% 91.49%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 91.79% 85.14%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.24% 95.56%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 89.28% 94.00%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 87.57% 92.62%
CHEMBL5608 Q16288 NT-3 growth factor receptor 87.25% 95.89%
CHEMBL1806 P11388 DNA topoisomerase II alpha 85.74% 89.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.95% 96.09%
CHEMBL1966 Q02127 Dihydroorotate dehydrogenase 84.62% 96.09%
CHEMBL4895 P30530 Tyrosine-protein kinase receptor UFO 84.09% 90.95%
CHEMBL4145 Q9UKV0 Histone deacetylase 9 81.80% 85.49%
CHEMBL2535 P11166 Glucose transporter 81.78% 98.75%
CHEMBL3492 P49721 Proteasome Macropain subunit 81.60% 90.24%
CHEMBL1293249 Q13887 Kruppel-like factor 5 80.50% 86.33%

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.
Lonchocarpus castilloi

Cross-Links

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PubChem 180424
LOTUS LTS0216963
wikiData Q82899975