(1S,3'R,4S,7R,10S)-3'-methyl-4-[(2S,4S)-4-methyl-5-oxooxolan-2-yl]spiro[11-oxa-5-azatricyclo[5.3.1.01,5]undecane-10,5'-oxolane]-2'-one

Details

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Internal ID ccfeaf1d-3ced-43f0-a51a-68451a26a528
Taxonomy Alkaloids and derivatives > Stemona alkaloids > Tuberostemospironine-type alkaloids
IUPAC Name (1S,3'R,4S,7R,10S)-3'-methyl-4-[(2S,4S)-4-methyl-5-oxooxolan-2-yl]spiro[11-oxa-5-azatricyclo[5.3.1.01,5]undecane-10,5'-oxolane]-2'-one
SMILES (Canonical) CC1CC(OC1=O)C2CCC34N2CC(O3)CCC45CC(C(=O)O5)C
SMILES (Isomeric) C[C@H]1C[C@H](OC1=O)[C@@H]2CC[C@]34N2C[C@H](O3)CC[C@]45C[C@H](C(=O)O5)C
InChI InChI=1S/C18H25NO5/c1-10-7-14(22-15(10)20)13-4-6-18-17(8-11(2)16(21)24-17)5-3-12(23-18)9-19(13)18/h10-14H,3-9H2,1-2H3/t10-,11+,12+,13-,14-,17-,18-/m0/s1
InChI Key GRCVOPKGGZCLPF-HMVZOGCKSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C18H25NO5
Molecular Weight 335.40 g/mol
Exact Mass 335.17327290 g/mol
Topological Polar Surface Area (TPSA) 65.10 Ų
XlogP 2.00
Atomic LogP (AlogP) 1.61
H-Bond Acceptor 6
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (1S,3'R,4S,7R,10S)-3'-methyl-4-[(2S,4S)-4-methyl-5-oxooxolan-2-yl]spiro[11-oxa-5-azatricyclo[5.3.1.01,5]undecane-10,5'-oxolane]-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 + 0.8402 84.02%
Caco-2 + 0.5243 52.43%
Blood Brain Barrier + 0.8000 80.00%
Human oral bioavailability + 0.6714 67.14%
Subcellular localzation Mitochondria 0.5919 59.19%
OATP2B1 inhibitior - 0.8563 85.63%
OATP1B1 inhibitior + 0.9113 91.13%
OATP1B3 inhibitior + 0.9450 94.50%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior - 0.6051 60.51%
P-glycoprotein inhibitior - 0.7371 73.71%
P-glycoprotein substrate + 0.5291 52.91%
CYP3A4 substrate + 0.6467 64.67%
CYP2C9 substrate - 0.8075 80.75%
CYP2D6 substrate - 0.8366 83.66%
CYP3A4 inhibition - 0.9433 94.33%
CYP2C9 inhibition - 0.8018 80.18%
CYP2C19 inhibition - 0.8061 80.61%
CYP2D6 inhibition - 0.9347 93.47%
CYP1A2 inhibition - 0.7204 72.04%
CYP2C8 inhibition - 0.8307 83.07%
CYP inhibitory promiscuity - 0.8898 88.98%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9200 92.00%
Carcinogenicity (trinary) Non-required 0.6370 63.70%
Eye corrosion - 0.9866 98.66%
Eye irritation - 0.9655 96.55%
Skin irritation - 0.7891 78.91%
Skin corrosion - 0.8885 88.85%
Ames mutagenesis - 0.7737 77.37%
Human Ether-a-go-go-Related Gene inhibition - 0.5794 57.94%
Micronuclear - 0.5400 54.00%
Hepatotoxicity + 0.5750 57.50%
skin sensitisation - 0.8619 86.19%
Respiratory toxicity + 0.7444 74.44%
Reproductive toxicity + 0.6889 68.89%
Mitochondrial toxicity + 0.8250 82.50%
Nephrotoxicity + 0.6185 61.85%
Acute Oral Toxicity (c) III 0.6641 66.41%
Estrogen receptor binding + 0.7326 73.26%
Androgen receptor binding + 0.7341 73.41%
Thyroid receptor binding - 0.4923 49.23%
Glucocorticoid receptor binding + 0.7750 77.50%
Aromatase binding + 0.6676 66.76%
PPAR gamma - 0.5646 56.46%
Honey bee toxicity - 0.7889 78.89%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity + 0.6800 68.00%
Fish aquatic toxicity - 0.3914 39.14%

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
CHEMBL204 P00734 Thrombin 95.75% 96.01%
CHEMBL253 P34972 Cannabinoid CB2 receptor 95.48% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.77% 96.09%
CHEMBL238 Q01959 Dopamine transporter 90.52% 95.88%
CHEMBL3137262 O60341 LSD1/CoREST complex 89.61% 97.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 89.14% 85.14%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 88.67% 93.40%
CHEMBL4588 P22894 Matrix metalloproteinase 8 86.41% 94.66%
CHEMBL1795139 Q8IU80 Transmembrane protease serine 6 86.41% 98.33%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 86.14% 93.04%
CHEMBL3746 P80365 11-beta-hydroxysteroid dehydrogenase 2 86.05% 94.78%
CHEMBL1871 P10275 Androgen Receptor 85.01% 96.43%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 84.23% 97.14%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 83.93% 96.77%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.75% 95.56%
CHEMBL4072 P07858 Cathepsin B 83.67% 93.67%
CHEMBL2730 P21980 Protein-glutamine gamma-glutamyltransferase 83.51% 92.38%
CHEMBL3012 Q13946 Phosphodiesterase 7A 82.89% 99.29%
CHEMBL1994 P08235 Mineralocorticoid receptor 82.48% 100.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.38% 95.89%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 82.34% 82.69%

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
Stemona mairei
Stemona tuberosa

Cross-Links

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PubChem 101160220
NPASS NPC233948
LOTUS LTS0205994
wikiData Q105015748