(4S)-4,4a,5,6,7,8,8a,9-Octahydro-3,4abeta,5beta-trimethyl-9-oxonaphtho[2,3-b]furan-4beta,8alpha,8abeta-triol 4-[(Z)-2-methyl-2-butenoate]8-acetate

Details

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Internal ID 6e35caeb-8f12-4398-8ade-faf37ebcd16d
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids > Eremophilane, 8,9-secoeremophilane and furoeremophilane sesquiterpenoids
IUPAC Name [(4S,4aS,5S,8S,8aS)-8-acetyloxy-8a-hydroxy-3,4a,5-trimethyl-9-oxo-5,6,7,8-tetrahydro-4H-benzo[f][1]benzofuran-4-yl] (Z)-2-methylbut-2-enoate
SMILES (Canonical) CC=C(C)C(=O)OC1C2=C(C(=O)C3(C1(C(CCC3OC(=O)C)C)C)O)OC=C2C
SMILES (Isomeric) C/C=C(/C)\C(=O)O[C@@H]1C2=C(C(=O)[C@@]3([C@]1([C@H](CC[C@@H]3OC(=O)C)C)C)O)OC=C2C
InChI InChI=1S/C22H28O7/c1-7-11(2)20(25)29-19-16-12(3)10-27-17(16)18(24)22(26)15(28-14(5)23)9-8-13(4)21(19,22)6/h7,10,13,15,19,26H,8-9H2,1-6H3/b11-7-/t13-,15-,19+,21-,22-/m0/s1
InChI Key NRBUYLCVCQRAEM-WUDAXFLVSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C22H28O7
Molecular Weight 404.50 g/mol
Exact Mass 404.18350323 g/mol
Topological Polar Surface Area (TPSA) 103.00 Ų
XlogP 3.20
Atomic LogP (AlogP) 3.43
H-Bond Acceptor 7
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (4S)-4,4a,5,6,7,8,8a,9-Octahydro-3,4abeta,5beta-trimethyl-9-oxonaphtho[2,3-b]furan-4beta,8alpha,8abeta-triol 4-[(Z)-2-methyl-2-butenoate]8-acetate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9893 98.93%
Caco-2 + 0.5642 56.42%
Blood Brain Barrier + 0.7250 72.50%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.7527 75.27%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8750 87.50%
OATP1B3 inhibitior - 0.3987 39.87%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.6353 63.53%
BSEP inhibitior + 0.7295 72.95%
P-glycoprotein inhibitior + 0.7025 70.25%
P-glycoprotein substrate - 0.7351 73.51%
CYP3A4 substrate + 0.6644 66.44%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8980 89.80%
CYP3A4 inhibition - 0.6866 68.66%
CYP2C9 inhibition - 0.6262 62.62%
CYP2C19 inhibition - 0.6639 66.39%
CYP2D6 inhibition - 0.9026 90.26%
CYP1A2 inhibition + 0.8104 81.04%
CYP2C8 inhibition + 0.5205 52.05%
CYP inhibitory promiscuity - 0.6831 68.31%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.4788 47.88%
Eye corrosion - 0.9922 99.22%
Eye irritation - 0.9270 92.70%
Skin irritation - 0.5619 56.19%
Skin corrosion - 0.8808 88.08%
Ames mutagenesis - 0.5500 55.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4300 43.00%
Micronuclear - 0.6600 66.00%
Hepatotoxicity + 0.5961 59.61%
skin sensitisation - 0.8070 80.70%
Respiratory toxicity + 0.5778 57.78%
Reproductive toxicity + 0.9222 92.22%
Mitochondrial toxicity + 0.7750 77.50%
Nephrotoxicity + 0.5000 50.00%
Acute Oral Toxicity (c) III 0.3483 34.83%
Estrogen receptor binding + 0.8169 81.69%
Androgen receptor binding + 0.6278 62.78%
Thyroid receptor binding + 0.6113 61.13%
Glucocorticoid receptor binding + 0.7519 75.19%
Aromatase binding + 0.5892 58.92%
PPAR gamma + 0.7343 73.43%
Honey bee toxicity - 0.7415 74.15%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity + 0.5700 57.00%
Fish aquatic toxicity + 0.9922 99.22%

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 98.10% 91.11%
CHEMBL1806 P11388 DNA topoisomerase II alpha 93.59% 89.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.68% 95.56%
CHEMBL3137262 O60341 LSD1/CoREST complex 90.71% 97.09%
CHEMBL4040 P28482 MAP kinase ERK2 88.55% 83.82%
CHEMBL241 Q14432 Phosphodiesterase 3A 88.10% 92.94%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.54% 86.33%
CHEMBL3492 P49721 Proteasome Macropain subunit 86.86% 90.24%
CHEMBL340 P08684 Cytochrome P450 3A4 85.75% 91.19%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 85.57% 94.80%
CHEMBL1994 P08235 Mineralocorticoid receptor 84.83% 100.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 83.85% 99.23%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 82.00% 94.45%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 81.82% 91.07%
CHEMBL1907601 P11802 Cyclin-dependent kinase 4/cyclin D1 81.42% 98.99%
CHEMBL1937 Q92769 Histone deacetylase 2 81.01% 94.75%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 80.87% 96.09%
CHEMBL4208 P20618 Proteasome component C5 80.87% 90.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.18% 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.
Jatropha curcas
Nepeta tenuifolia
Senecio dryophyllus

Cross-Links

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PubChem 101606405
NPASS NPC160858
LOTUS LTS0038345
wikiData Q105184319