(5Z)-5-[(1S,4S,5R,6S,8S,13R)-9-[(2S)-2-hydroxybutyl]-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 401f7def-5fcb-43e1-b366-bb07147f1304
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbohydrates and carbohydrate conjugates > Aminosaccharides > Aminoglycosides
IUPAC Name (5Z)-5-[(1S,4S,5R,6S,8S,13R)-9-[(2S)-2-hydroxybutyl]-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) CCC(CC12C3CCN1C4CC2OC35C4C(C(=C6C(=C(C(=O)O6)C)OC)O5)C)O
SMILES (Isomeric) CC[C@@H](CC12[C@H]3CCN1[C@H]4C[C@@H]2O[C@]35[C@@H]4[C@@H](/C(=C/6\C(=C(C(=O)O6)C)OC)/O5)C)O
InChI InChI=1S/C22H29NO6/c1-5-12(24)9-21-14-6-7-23(21)13-8-15(21)28-22(14)16(13)10(2)18(29-22)19-17(26-4)11(3)20(25)27-19/h10,12-16,24H,5-9H2,1-4H3/b19-18-/t10-,12-,13-,14+,15-,16+,21?,22+/m0/s1
InChI Key WXCVDEUJZBRYIT-BYEHHIJUSA-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 1.80
Atomic LogP (AlogP) 2.06
H-Bond Acceptor 7
H-Bond Donor 1
Rotatable Bonds 4

Synonyms

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Q27137732

2D Structure

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2D Structure of (5Z)-5-[(1S,4S,5R,6S,8S,13R)-9-[(2S)-2-hydroxybutyl]-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 + 0.9461 94.61%
Caco-2 + 0.6094 60.94%
Blood Brain Barrier + 0.7500 75.00%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Mitochondria 0.5702 57.02%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8898 88.98%
OATP1B3 inhibitior + 0.9383 93.83%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior + 0.7697 76.97%
P-glycoprotein inhibitior - 0.5566 55.66%
P-glycoprotein substrate + 0.5409 54.09%
CYP3A4 substrate + 0.6544 65.44%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8032 80.32%
CYP3A4 inhibition - 0.9226 92.26%
CYP2C9 inhibition - 0.9016 90.16%
CYP2C19 inhibition - 0.9117 91.17%
CYP2D6 inhibition - 0.8900 89.00%
CYP1A2 inhibition - 0.8741 87.41%
CYP2C8 inhibition - 0.6503 65.03%
CYP inhibitory promiscuity - 0.8658 86.58%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.4822 48.22%
Eye corrosion - 0.9874 98.74%
Eye irritation - 0.9316 93.16%
Skin irritation - 0.7467 74.67%
Skin corrosion - 0.9275 92.75%
Ames mutagenesis - 0.6400 64.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4367 43.67%
Micronuclear + 0.6200 62.00%
Hepatotoxicity - 0.6079 60.79%
skin sensitisation - 0.8450 84.50%
Respiratory toxicity + 0.7778 77.78%
Reproductive toxicity + 0.9222 92.22%
Mitochondrial toxicity + 0.9000 90.00%
Nephrotoxicity - 0.5719 57.19%
Acute Oral Toxicity (c) III 0.5403 54.03%
Estrogen receptor binding + 0.8444 84.44%
Androgen receptor binding + 0.7214 72.14%
Thyroid receptor binding + 0.6918 69.18%
Glucocorticoid receptor binding + 0.6780 67.80%
Aromatase binding + 0.6301 63.01%
PPAR gamma + 0.6134 61.34%
Honey bee toxicity - 0.7722 77.22%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.5800 58.00%
Fish aquatic toxicity + 0.7535 75.35%

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 98.61% 96.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 98.48% 85.14%
CHEMBL2581 P07339 Cathepsin D 97.08% 98.95%
CHEMBL253 P34972 Cannabinoid CB2 receptor 96.10% 97.25%
CHEMBL218 P21554 Cannabinoid CB1 receptor 95.33% 96.61%
CHEMBL4588 P22894 Matrix metalloproteinase 8 92.67% 94.66%
CHEMBL3137262 O60341 LSD1/CoREST complex 91.11% 97.09%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 88.82% 97.14%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 88.58% 91.11%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 87.67% 94.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 87.10% 95.89%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.66% 95.56%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 86.44% 99.23%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.67% 86.33%
CHEMBL221 P23219 Cyclooxygenase-1 84.78% 90.17%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 83.73% 96.47%
CHEMBL3192 Q9BY41 Histone deacetylase 8 83.52% 93.99%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 82.64% 95.89%
CHEMBL1871 P10275 Androgen Receptor 82.17% 96.43%
CHEMBL4581 P52732 Kinesin-like protein 1 80.61% 93.18%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 80.35% 100.00%

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 burkillii
Stemona cochinchinensis
Stemona collinsae

Cross-Links

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PubChem 139031609
LOTUS LTS0269688
wikiData Q27137732