(5Z)-5-[(1R,4S,5R,6R,9S,12S,13S)-9-butyl-12-hydroxy-4-methyl-2,14-dioxa-10-azapentacyclo[6.5.1.01,5.06,10.09,13]tetradecan-3-ylidene]-4-methoxy-3-methylfuran-2-one

Details

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Internal ID e0fa2047-1e81-4465-a7d9-ca4dea64163f
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbohydrates and carbohydrate conjugates > Aminosaccharides > Aminoglycosides
IUPAC Name (5Z)-5-[(1R,4S,5R,6R,9S,12S,13S)-9-butyl-12-hydroxy-4-methyl-2,14-dioxa-10-azapentacyclo[6.5.1.01,5.06,10.09,13]tetradecan-3-ylidene]-4-methoxy-3-methylfuran-2-one
SMILES (Canonical) CCCCC12C3CC4N1CC(C2C5(C4C(C(=C6C(=C(C(=O)O6)C)OC)O5)C)O3)O
SMILES (Isomeric) CCCC[C@@]12[C@H]3[C@@H](CN1[C@@H]4CC2O[C@@]35[C@@H]4[C@@H](/C(=C/6\C(=C(C(=O)O6)C)OC)/O5)C)O
InChI InChI=1S/C22H29NO6/c1-5-6-7-21-14-8-12-15-10(2)17(18-16(26-4)11(3)20(25)27-18)29-22(15,28-14)19(21)13(24)9-23(12)21/h10,12-15,19,24H,5-9H2,1-4H3/b18-17-/t10-,12+,13+,14?,15+,19+,21+,22+/m0/s1
InChI Key JCWCJMDFKZQWQK-JACSAYKJSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C22H29NO6
Molecular Weight 403.50 g/mol
Exact Mass 403.19948764 g/mol
Topological Polar Surface Area (TPSA) 77.50 Ų
XlogP 1.90
Atomic LogP (AlogP) 2.06
H-Bond Acceptor 7
H-Bond Donor 1
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (5Z)-5-[(1R,4S,5R,6R,9S,12S,13S)-9-butyl-12-hydroxy-4-methyl-2,14-dioxa-10-azapentacyclo[6.5.1.01,5.06,10.09,13]tetradecan-3-ylidene]-4-methoxy-3-methylfuran-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 + 0.9122 91.22%
Caco-2 + 0.5662 56.62%
Blood Brain Barrier + 0.8000 80.00%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Mitochondria 0.5191 51.91%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8723 87.23%
OATP1B3 inhibitior + 0.9370 93.70%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior + 0.8332 83.32%
P-glycoprotein inhibitior - 0.5780 57.80%
P-glycoprotein substrate + 0.6442 64.42%
CYP3A4 substrate + 0.6769 67.69%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7987 79.87%
CYP3A4 inhibition - 0.9238 92.38%
CYP2C9 inhibition - 0.8783 87.83%
CYP2C19 inhibition - 0.8987 89.87%
CYP2D6 inhibition - 0.8939 89.39%
CYP1A2 inhibition - 0.8677 86.77%
CYP2C8 inhibition - 0.6618 66.18%
CYP inhibitory promiscuity - 0.8303 83.03%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.4635 46.35%
Eye corrosion - 0.9879 98.79%
Eye irritation - 0.9385 93.85%
Skin irritation - 0.7245 72.45%
Skin corrosion - 0.9251 92.51%
Ames mutagenesis - 0.5600 56.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5000 50.00%
Micronuclear + 0.5600 56.00%
Hepatotoxicity - 0.5247 52.47%
skin sensitisation - 0.8538 85.38%
Respiratory toxicity + 0.7000 70.00%
Reproductive toxicity + 0.9222 92.22%
Mitochondrial toxicity + 0.9375 93.75%
Nephrotoxicity + 0.5584 55.84%
Acute Oral Toxicity (c) III 0.5251 52.51%
Estrogen receptor binding + 0.8230 82.30%
Androgen receptor binding + 0.7302 73.02%
Thyroid receptor binding + 0.6718 67.18%
Glucocorticoid receptor binding + 0.7808 78.08%
Aromatase binding + 0.6251 62.51%
PPAR gamma + 0.6811 68.11%
Honey bee toxicity - 0.8509 85.09%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity + 0.5868 58.68%
Fish aquatic toxicity + 0.8748 87.48%

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 98.63% 96.09%
CHEMBL218 P21554 Cannabinoid CB1 receptor 98.14% 96.61%
CHEMBL2581 P07339 Cathepsin D 98.06% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.67% 91.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 92.64% 85.14%
CHEMBL253 P34972 Cannabinoid CB2 receptor 89.89% 97.25%
CHEMBL3137262 O60341 LSD1/CoREST complex 89.87% 97.09%
CHEMBL2069156 Q14145 Kelch-like ECH-associated protein 1 89.81% 82.38%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.51% 86.33%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 88.48% 99.23%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.15% 95.56%
CHEMBL221 P23219 Cyclooxygenase-1 87.35% 90.17%
CHEMBL299 P17252 Protein kinase C alpha 86.15% 98.03%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 84.95% 97.14%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 84.16% 94.00%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 84.02% 100.00%
CHEMBL4588 P22894 Matrix metalloproteinase 8 83.97% 94.66%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 81.29% 93.00%

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.
Stemona japonica

Cross-Links

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PubChem 163185528
LOTUS LTS0229576
wikiData Q105125179