methyl 7-(1,2-dihydroxy-6-methoxy-6-oxohex-4-enyl)-9-(2-hexyl-5-oxo-2H-furan-4-yl)-4-(hydroxymethylidene)-1,3-dioxo-2-oxaspiro[4.4]nonane-9-carboxylate

Details

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Internal ID 7b996e3d-55ac-4b18-b2bd-39aef9e25303
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Terpene lactones
IUPAC Name methyl 7-(1,2-dihydroxy-6-methoxy-6-oxohex-4-enyl)-9-(2-hexyl-5-oxo-2H-furan-4-yl)-4-(hydroxymethylidene)-1,3-dioxo-2-oxaspiro[4.4]nonane-9-carboxylate
SMILES (Canonical) CCCCCCC1C=C(C(=O)O1)C2(CC(CC23C(=CO)C(=O)OC3=O)C(C(CC=CC(=O)OC)O)O)C(=O)OC
SMILES (Isomeric) CCCCCCC1C=C(C(=O)O1)C2(CC(CC23C(=CO)C(=O)OC3=O)C(C(CC=CC(=O)OC)O)O)C(=O)OC
InChI InChI=1S/C28H36O12/c1-4-5-6-7-9-17-12-18(23(33)39-17)27(25(35)38-3)13-16(22(32)20(30)10-8-11-21(31)37-2)14-28(27)19(15-29)24(34)40-26(28)36/h8,11-12,15-17,20,22,29-30,32H,4-7,9-10,13-14H2,1-3H3
InChI Key ULUMNLCJERAXQP-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C28H36O12
Molecular Weight 564.60 g/mol
Exact Mass 564.22067658 g/mol
Topological Polar Surface Area (TPSA) 183.00 Ų
XlogP 2.60
Atomic LogP (AlogP) 1.73
H-Bond Acceptor 12
H-Bond Donor 3
Rotatable Bonds 12

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of methyl 7-(1,2-dihydroxy-6-methoxy-6-oxohex-4-enyl)-9-(2-hexyl-5-oxo-2H-furan-4-yl)-4-(hydroxymethylidene)-1,3-dioxo-2-oxaspiro[4.4]nonane-9-carboxylate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9547 95.47%
Caco-2 - 0.7936 79.36%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability - 0.7857 78.57%
Subcellular localzation Mitochondria 0.7013 70.13%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8151 81.51%
OATP1B3 inhibitior + 0.8904 89.04%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior + 0.9796 97.96%
P-glycoprotein inhibitior + 0.8265 82.65%
P-glycoprotein substrate + 0.6304 63.04%
CYP3A4 substrate + 0.7139 71.39%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8813 88.13%
CYP3A4 inhibition + 0.5372 53.72%
CYP2C9 inhibition - 0.6578 65.78%
CYP2C19 inhibition - 0.6275 62.75%
CYP2D6 inhibition - 0.9350 93.50%
CYP1A2 inhibition - 0.7001 70.01%
CYP2C8 inhibition + 0.6560 65.60%
CYP inhibitory promiscuity - 0.9468 94.68%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.5088 50.88%
Eye corrosion - 0.9881 98.81%
Eye irritation - 0.9315 93.15%
Skin irritation - 0.5382 53.82%
Skin corrosion - 0.9294 92.94%
Ames mutagenesis - 0.7200 72.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4464 44.64%
Micronuclear - 0.7400 74.00%
Hepatotoxicity - 0.5755 57.55%
skin sensitisation - 0.8778 87.78%
Respiratory toxicity + 0.7222 72.22%
Reproductive toxicity + 0.8111 81.11%
Mitochondrial toxicity + 0.8250 82.50%
Nephrotoxicity - 0.6281 62.81%
Acute Oral Toxicity (c) II 0.5525 55.25%
Estrogen receptor binding + 0.7938 79.38%
Androgen receptor binding + 0.6951 69.51%
Thyroid receptor binding - 0.5753 57.53%
Glucocorticoid receptor binding + 0.7571 75.71%
Aromatase binding + 0.5645 56.45%
PPAR gamma + 0.5624 56.24%
Honey bee toxicity - 0.8174 81.74%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity + 0.6925 69.25%
Fish aquatic toxicity + 0.9716 97.16%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.84% 96.09%
CHEMBL2581 P07339 Cathepsin D 96.72% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.69% 95.56%
CHEMBL3060 Q9Y345 Glycine transporter 2 94.38% 99.17%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.27% 91.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.95% 86.33%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 87.62% 99.23%
CHEMBL230 P35354 Cyclooxygenase-2 87.60% 89.63%
CHEMBL221 P23219 Cyclooxygenase-1 87.42% 90.17%
CHEMBL1907605 P24864 Cyclin-dependent kinase 2/cyclin E1 85.92% 92.88%
CHEMBL3401 O75469 Pregnane X receptor 84.01% 94.73%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 83.35% 94.45%
CHEMBL4227 P25090 Lipoxin A4 receptor 83.29% 100.00%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 82.99% 92.62%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 82.86% 97.14%
CHEMBL340 P08684 Cytochrome P450 3A4 82.64% 91.19%
CHEMBL3137262 O60341 LSD1/CoREST complex 81.21% 97.09%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 80.96% 95.50%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 80.81% 94.33%
CHEMBL5103 Q969S8 Histone deacetylase 10 80.60% 90.08%

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 162932169
LOTUS LTS0225296
wikiData Q104198353