5-(4a-methyl-8-methylidene-1,2,3,4,5,6,7,8a-octahydronaphthalen-2-yl)-5',8'a-dimethylspiro[3,4-dihydropyran-2,3'-5,6,7,8,9,9a-hexahydro-3aH-benzo[f][1]benzofuran]-2'-one

Details

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Internal ID cfb0acd5-db90-403c-90fe-456c329cf59f
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Terpene lactones > Sesquiterpene lactones > Eudesmanolides, secoeudesmanolides, and derivatives
IUPAC Name 5-(4a-methyl-8-methylidene-1,2,3,4,5,6,7,8a-octahydronaphthalen-2-yl)-5',8'a-dimethylspiro[3,4-dihydropyran-2,3'-5,6,7,8,9,9a-hexahydro-3aH-benzo[f][1]benzofuran]-2'-one
SMILES (Canonical) CC1CCCC2(C1=CC3C(C2)OC(=O)C34CCC(=CO4)C5CCC6(CCCC(=C)C6C5)C)C
SMILES (Isomeric) CC1CCCC2(C1=CC3C(C2)OC(=O)C34CCC(=CO4)C5CCC6(CCCC(=C)C6C5)C)C
InChI InChI=1S/C30H42O3/c1-19-7-5-11-28(3)13-9-21(15-23(19)28)22-10-14-30(32-18-22)25-16-24-20(2)8-6-12-29(24,4)17-26(25)33-27(30)31/h16,18,20-21,23,25-26H,1,5-15,17H2,2-4H3
InChI Key GQVQCJCFCSLJQU-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C30H42O3
Molecular Weight 450.70 g/mol
Exact Mass 450.31339520 g/mol
Topological Polar Surface Area (TPSA) 35.50 Ų
XlogP 7.20
Atomic LogP (AlogP) 7.28
H-Bond Acceptor 3
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 5-(4a-methyl-8-methylidene-1,2,3,4,5,6,7,8a-octahydronaphthalen-2-yl)-5',8'a-dimethylspiro[3,4-dihydropyran-2,3'-5,6,7,8,9,9a-hexahydro-3aH-benzo[f][1]benzofuran]-2'-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9951 99.51%
Caco-2 - 0.5237 52.37%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability + 0.5286 52.86%
Subcellular localzation Mitochondria 0.6313 63.13%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8626 86.26%
OATP1B3 inhibitior + 0.8628 86.28%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior + 0.5250 52.50%
BSEP inhibitior + 0.8589 85.89%
P-glycoprotein inhibitior + 0.7583 75.83%
P-glycoprotein substrate - 0.5051 50.51%
CYP3A4 substrate + 0.6984 69.84%
CYP2C9 substrate - 0.6110 61.10%
CYP2D6 substrate - 0.8147 81.47%
CYP3A4 inhibition - 0.7427 74.27%
CYP2C9 inhibition - 0.8814 88.14%
CYP2C19 inhibition - 0.7822 78.22%
CYP2D6 inhibition - 0.9323 93.23%
CYP1A2 inhibition - 0.6005 60.05%
CYP2C8 inhibition + 0.5656 56.56%
CYP inhibitory promiscuity - 0.8462 84.62%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.5061 50.61%
Eye corrosion - 0.9820 98.20%
Eye irritation - 0.9457 94.57%
Skin irritation - 0.5847 58.47%
Skin corrosion - 0.9133 91.33%
Ames mutagenesis - 0.5600 56.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8018 80.18%
Micronuclear - 0.8100 81.00%
Hepatotoxicity + 0.6500 65.00%
skin sensitisation - 0.7710 77.10%
Respiratory toxicity + 0.6778 67.78%
Reproductive toxicity + 0.8222 82.22%
Mitochondrial toxicity + 0.7500 75.00%
Nephrotoxicity + 0.4640 46.40%
Acute Oral Toxicity (c) III 0.4577 45.77%
Estrogen receptor binding + 0.6517 65.17%
Androgen receptor binding + 0.7135 71.35%
Thyroid receptor binding + 0.5543 55.43%
Glucocorticoid receptor binding + 0.7983 79.83%
Aromatase binding + 0.6925 69.25%
PPAR gamma - 0.5422 54.22%
Honey bee toxicity - 0.7264 72.64%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity + 0.7053 70.53%
Fish aquatic toxicity + 0.9875 98.75%

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 94.76% 97.25%
CHEMBL3137262 O60341 LSD1/CoREST complex 93.91% 97.09%
CHEMBL241 Q14432 Phosphodiesterase 3A 92.64% 92.94%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 91.59% 93.40%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.59% 95.56%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 88.61% 99.23%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 87.24% 82.69%
CHEMBL1994 P08235 Mineralocorticoid receptor 87.23% 100.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 87.07% 94.45%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 86.85% 91.11%
CHEMBL3045 P05771 Protein kinase C beta 86.26% 97.63%
CHEMBL259 P32245 Melanocortin receptor 4 85.73% 95.38%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.73% 96.09%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 85.40% 96.77%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 84.04% 97.14%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.83% 86.33%
CHEMBL221 P23219 Cyclooxygenase-1 82.30% 90.17%
CHEMBL3746 P80365 11-beta-hydroxysteroid dehydrogenase 2 81.04% 94.78%
CHEMBL1806 P11388 DNA topoisomerase II alpha 80.35% 89.00%
CHEMBL4530 P00488 Coagulation factor XIII 80.28% 96.00%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 80.22% 93.04%

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.
Helenium autumnale
Umbilicus rupestris

Cross-Links

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PubChem 14315675
LOTUS LTS0230470
wikiData Q105161078