Bacchotricuneatin B

Details

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Internal ID cde5c14e-6849-471a-bf76-0f424f7d17c3
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Terpene lactones > Diterpene lactones
IUPAC Name 5'-(furan-3-yl)-8-methylspiro[5,6,6a,8,9,10-hexahydro-1H-benzo[d][2]benzofuran-7,3'-oxolane]-2',3-dione
SMILES (Canonical) CC1CCC23COC(=O)C2=CCCC3C14CC(OC4=O)C5=COC=C5
SMILES (Isomeric) CC1CCC23COC(=O)C2=CCCC3C14CC(OC4=O)C5=COC=C5
InChI InChI=1S/C20H22O5/c1-12-5-7-19-11-24-17(21)14(19)3-2-4-16(19)20(12)9-15(25-18(20)22)13-6-8-23-10-13/h3,6,8,10,12,15-16H,2,4-5,7,9,11H2,1H3
InChI Key HMAABAHMPJEWDJ-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C20H22O5
Molecular Weight 342.40 g/mol
Exact Mass 342.14672380 g/mol
Topological Polar Surface Area (TPSA) 65.70 Ų
XlogP 3.20
Atomic LogP (AlogP) 3.56
H-Bond Acceptor 5
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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65596-26-1
NSC299116
DTXSID90316061
HMAABAHMPJEWDJ-UHFFFAOYSA-N
NSC-299116
Spiro[furan-3(2H),7'(8'H)-[1H]naphtho[1,8a-c]furan]-2,3'(5'H)-dione, 5-(3-furanyl)-4,5,6',6'a,9',10'-hexahydro-8'-methyl-, [6'aS-[6'a.alpha.,7'.beta.(S*),8'.beta.,10'aR*]]-
Spiro[furan-3(2H),8a-c]furan]-2,3'(5'H)-dione, 5-(3-furanyl)-4,5,6',6'a,9',10'-hexahydro-8'-methyl-, [6'aS-[6'a.alpha.,7'.beta.(S*),8'.beta.,10'aR*]]-

2D Structure

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2D Structure of Bacchotricuneatin B

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 + 0.6128 61.28%
Blood Brain Barrier + 0.7500 75.00%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Mitochondria 0.8237 82.37%
OATP2B1 inhibitior - 0.8606 86.06%
OATP1B1 inhibitior + 0.8693 86.93%
OATP1B3 inhibitior + 0.9582 95.82%
MATE1 inhibitior - 0.8000 80.00%
OCT2 inhibitior - 0.5500 55.00%
BSEP inhibitior - 0.6256 62.56%
P-glycoprotein inhibitior - 0.6699 66.99%
P-glycoprotein substrate - 0.6808 68.08%
CYP3A4 substrate + 0.6288 62.88%
CYP2C9 substrate - 0.7990 79.90%
CYP2D6 substrate - 0.8693 86.93%
CYP3A4 inhibition - 0.6318 63.18%
CYP2C9 inhibition - 0.7518 75.18%
CYP2C19 inhibition - 0.8079 80.79%
CYP2D6 inhibition - 0.9001 90.01%
CYP1A2 inhibition - 0.7117 71.17%
CYP2C8 inhibition + 0.4856 48.56%
CYP inhibitory promiscuity - 0.7768 77.68%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Non-required 0.4366 43.66%
Eye corrosion - 0.9802 98.02%
Eye irritation - 0.9451 94.51%
Skin irritation - 0.6613 66.13%
Skin corrosion - 0.9315 93.15%
Ames mutagenesis - 0.5070 50.70%
Human Ether-a-go-go-Related Gene inhibition + 0.8007 80.07%
Micronuclear - 0.6800 68.00%
Hepatotoxicity + 0.6052 60.52%
skin sensitisation - 0.8782 87.82%
Respiratory toxicity + 0.7000 70.00%
Reproductive toxicity + 0.8222 82.22%
Mitochondrial toxicity + 0.6000 60.00%
Nephrotoxicity + 0.7600 76.00%
Acute Oral Toxicity (c) III 0.5009 50.09%
Estrogen receptor binding + 0.8827 88.27%
Androgen receptor binding + 0.6393 63.93%
Thyroid receptor binding - 0.6082 60.82%
Glucocorticoid receptor binding + 0.6099 60.99%
Aromatase binding + 0.7148 71.48%
PPAR gamma - 0.4897 48.97%
Honey bee toxicity - 0.8724 87.24%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity + 0.6400 64.00%
Fish aquatic toxicity + 0.9971 99.71%

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
CHEMBL3137262 O60341 LSD1/CoREST complex 94.29% 97.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.19% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.57% 91.11%
CHEMBL221 P23219 Cyclooxygenase-1 89.83% 90.17%
CHEMBL253 P34972 Cannabinoid CB2 receptor 89.72% 97.25%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 88.86% 99.23%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 87.61% 82.69%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 85.75% 93.40%
CHEMBL1994 P08235 Mineralocorticoid receptor 85.33% 100.00%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 84.26% 97.14%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 82.70% 94.80%
CHEMBL1293249 Q13887 Kruppel-like factor 5 82.38% 86.33%
CHEMBL2581 P07339 Cathepsin D 81.94% 98.95%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 80.27% 94.00%

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.
Baccharis linearifolia subsp. chilco
Baccharis tricuneata

Cross-Links

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PubChem 326833
LOTUS LTS0012769
wikiData Q82069590