[6-[5-(1,2,4a,5-tetramethyl-2,3,4,7,8,8a-hexahydronaphthalen-1-yl)-3-methylpent-2-enyl]-6,6a-dihydroxy-5-oxo-3,3a-dihydro-2H-furo[3,2-b]furan-3-yl] acetate

Details

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Internal ID 65bc6190-3964-4069-b069-3c56c3f5d4db
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Terpene lactones > Diterpene lactones
IUPAC Name [6-[5-(1,2,4a,5-tetramethyl-2,3,4,7,8,8a-hexahydronaphthalen-1-yl)-3-methylpent-2-enyl]-6,6a-dihydroxy-5-oxo-3,3a-dihydro-2H-furo[3,2-b]furan-3-yl] acetate
SMILES (Canonical) CC1CCC2(C(C1(C)CCC(=CCC3(C(=O)OC4C3(OCC4OC(=O)C)O)O)C)CCC=C2C)C
SMILES (Isomeric) CC1CCC2(C(C1(C)CCC(=CCC3(C(=O)OC4C3(OCC4OC(=O)C)O)O)C)CCC=C2C)C
InChI InChI=1S/C28H42O7/c1-17(10-13-25(5)19(3)12-14-26(6)18(2)8-7-9-22(25)26)11-15-27(31)24(30)35-23-21(34-20(4)29)16-33-28(23,27)32/h8,11,19,21-23,31-32H,7,9-10,12-16H2,1-6H3
InChI Key UNRGCEXOJBFAII-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C28H42O7
Molecular Weight 490.60 g/mol
Exact Mass 490.29305367 g/mol
Topological Polar Surface Area (TPSA) 102.00 Ų
XlogP 4.90
Atomic LogP (AlogP) 4.21
H-Bond Acceptor 7
H-Bond Donor 2
Rotatable Bonds 6

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of [6-[5-(1,2,4a,5-tetramethyl-2,3,4,7,8,8a-hexahydronaphthalen-1-yl)-3-methylpent-2-enyl]-6,6a-dihydroxy-5-oxo-3,3a-dihydro-2H-furo[3,2-b]furan-3-yl] acetate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9619 96.19%
Caco-2 - 0.6911 69.11%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Mitochondria 0.8573 85.73%
OATP2B1 inhibitior - 0.7154 71.54%
OATP1B1 inhibitior + 0.8725 87.25%
OATP1B3 inhibitior + 0.9437 94.37%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.6553 65.53%
BSEP inhibitior + 0.6968 69.68%
P-glycoprotein inhibitior + 0.6876 68.76%
P-glycoprotein substrate - 0.5994 59.94%
CYP3A4 substrate + 0.6995 69.95%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8856 88.56%
CYP3A4 inhibition - 0.6410 64.10%
CYP2C9 inhibition - 0.8152 81.52%
CYP2C19 inhibition - 0.9151 91.51%
CYP2D6 inhibition - 0.9526 95.26%
CYP1A2 inhibition - 0.8750 87.50%
CYP2C8 inhibition + 0.5506 55.06%
CYP inhibitory promiscuity - 0.9336 93.36%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Non-required 0.4393 43.93%
Eye corrosion - 0.9923 99.23%
Eye irritation - 0.9282 92.82%
Skin irritation + 0.6847 68.47%
Skin corrosion - 0.9393 93.93%
Ames mutagenesis + 0.5134 51.34%
Human Ether-a-go-go-Related Gene inhibition - 0.5234 52.34%
Micronuclear - 0.7900 79.00%
Hepatotoxicity + 0.5250 52.50%
skin sensitisation - 0.9259 92.59%
Respiratory toxicity + 0.5778 57.78%
Reproductive toxicity + 0.9111 91.11%
Mitochondrial toxicity + 0.8500 85.00%
Nephrotoxicity + 0.5461 54.61%
Acute Oral Toxicity (c) I 0.5122 51.22%
Estrogen receptor binding + 0.7040 70.40%
Androgen receptor binding + 0.7270 72.70%
Thyroid receptor binding + 0.6197 61.97%
Glucocorticoid receptor binding + 0.8020 80.20%
Aromatase binding + 0.7209 72.09%
PPAR gamma + 0.5740 57.40%
Honey bee toxicity - 0.7342 73.42%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.5200 52.00%
Fish aquatic toxicity + 0.9905 99.05%

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 96.47% 91.11%
CHEMBL253 P34972 Cannabinoid CB2 receptor 94.68% 97.25%
CHEMBL4040 P28482 MAP kinase ERK2 93.73% 83.82%
CHEMBL1293255 P15428 15-hydroxyprostaglandin dehydrogenase [NAD+] 92.49% 83.57%
CHEMBL2581 P07339 Cathepsin D 90.47% 98.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 89.61% 94.45%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.85% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 87.89% 97.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.88% 95.56%
CHEMBL1806 P11388 DNA topoisomerase II alpha 87.82% 89.00%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 87.50% 94.80%
CHEMBL1994 P08235 Mineralocorticoid receptor 86.45% 100.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.74% 86.33%
CHEMBL340 P08684 Cytochrome P450 3A4 84.84% 91.19%
CHEMBL241 Q14432 Phosphodiesterase 3A 84.39% 92.94%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 82.40% 91.07%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.93% 99.23%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 81.76% 93.00%
CHEMBL5028 O14672 ADAM10 81.30% 97.50%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.13% 95.89%

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.
Brachyglottis bidwillii

Cross-Links

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PubChem 85142209
LOTUS LTS0197550
wikiData Q105276113