NCGC00169365-03_C25H32O8_5H-Furo[3,4-i]oxepino[4,3-a]xanthene-3,12-dione, 1,2,5a,6,7,7a,10,14,14a,14b-decahydro-5a,6-dihydroxy-13-methoxy-5,5,7a,9,14b-pentamethyl-

Details

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Internal ID c24fa105-e856-4eec-bac3-7fc3f35dfaf7
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthenes
IUPAC Name 20,21-dihydroxy-10-methoxy-1,4,14,19,19-pentamethyl-2,7,18-trioxapentacyclo[11.9.0.03,11.05,9.014,20]docosa-3(11),4,9-triene-8,17-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C25H32O8/c1-12-14-11-31-21(28)18(14)20(30-6)13-9-15-23(4)8-7-17(27)32-22(2,3)25(23,29)16(26)10-24(15,5)33-19(12)13/h15-16,26,29H,7-11H2,1-6H3
InChI Key ZVTVYIVILDSYIK-UHFFFAOYSA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C25H32O8
Molecular Weight 460.50 g/mol
Exact Mass 460.20971797 g/mol
Topological Polar Surface Area (TPSA) 112.00 Ų
XlogP 2.10
Atomic LogP (AlogP) 2.60
H-Bond Acceptor 8
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

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ACon1_000781
AKOS040739997
NCGC00169365-01
NCGC00169365-03
BRD-A63422794-001-01-5
NCGC00169365-03_C25H32O8_5H-Furo[3,4-i]oxepino[4,3-a]xanthene-3,12-dione, 1,2,5a,6,7,7a,10,14,14a,14b-decahydro-5a,6-dihydroxy-13-methoxy-5,5,7a,9,14b-pentamethyl-

2D Structure

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2D Structure of NCGC00169365-03_C25H32O8_5H-Furo[3,4-i]oxepino[4,3-a]xanthene-3,12-dione, 1,2,5a,6,7,7a,10,14,14a,14b-decahydro-5a,6-dihydroxy-13-methoxy-5,5,7a,9,14b-pentamethyl-

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9314 93.14%
Caco-2 - 0.5430 54.30%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability - 0.7000 70.00%
Subcellular localzation Mitochondria 0.7891 78.91%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9046 90.46%
OATP1B3 inhibitior + 0.8718 87.18%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior + 0.9172 91.72%
P-glycoprotein inhibitior - 0.4350 43.50%
P-glycoprotein substrate - 0.6473 64.73%
CYP3A4 substrate + 0.6939 69.39%
CYP2C9 substrate - 0.7965 79.65%
CYP2D6 substrate - 0.8524 85.24%
CYP3A4 inhibition - 0.6908 69.08%
CYP2C9 inhibition - 0.8033 80.33%
CYP2C19 inhibition - 0.8080 80.80%
CYP2D6 inhibition - 0.9372 93.72%
CYP1A2 inhibition - 0.6143 61.43%
CYP2C8 inhibition + 0.5697 56.97%
CYP inhibitory promiscuity - 0.9742 97.42%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9200 92.00%
Carcinogenicity (trinary) Non-required 0.5714 57.14%
Eye corrosion - 0.9906 99.06%
Eye irritation - 0.7881 78.81%
Skin irritation - 0.7503 75.03%
Skin corrosion - 0.9379 93.79%
Ames mutagenesis + 0.5800 58.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6987 69.87%
Micronuclear - 0.7700 77.00%
Hepatotoxicity - 0.5123 51.23%
skin sensitisation - 0.8941 89.41%
Respiratory toxicity + 0.6333 63.33%
Reproductive toxicity + 0.8778 87.78%
Mitochondrial toxicity + 0.7625 76.25%
Nephrotoxicity + 0.5222 52.22%
Acute Oral Toxicity (c) II 0.3307 33.07%
Estrogen receptor binding + 0.8176 81.76%
Androgen receptor binding + 0.7132 71.32%
Thyroid receptor binding + 0.5754 57.54%
Glucocorticoid receptor binding + 0.8404 84.04%
Aromatase binding + 0.8696 86.96%
PPAR gamma + 0.6462 64.62%
Honey bee toxicity - 0.7745 77.45%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity + 0.5400 54.00%
Fish aquatic toxicity + 0.9845 98.45%

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 97.95% 91.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 94.29% 85.14%
CHEMBL4302 P08183 P-glycoprotein 1 93.89% 92.98%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.03% 95.56%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 92.92% 94.45%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.24% 86.33%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 90.02% 99.23%
CHEMBL3137262 O60341 LSD1/CoREST complex 87.61% 97.09%
CHEMBL2581 P07339 Cathepsin D 87.39% 98.95%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 86.99% 97.14%
CHEMBL1994 P08235 Mineralocorticoid receptor 86.17% 100.00%
CHEMBL4681 P42330 Aldo-keto-reductase family 1 member C3 86.14% 89.05%
CHEMBL2002 P12268 Inosine-5'-monophosphate dehydrogenase 2 85.75% 98.21%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.19% 96.09%
CHEMBL1806 P11388 DNA topoisomerase II alpha 84.73% 89.00%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 82.92% 92.62%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 82.62% 96.77%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 81.15% 96.95%

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.
There are no matching plants.

Cross-Links

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PubChem 23846522
LOTUS LTS0114564
wikiData Q104202845