(1R,3'aS,4S,8S,9R,10R,12R)-2'-ethoxy-3',3'a-dihydroxy-4,8,10-trimethylspiro[2-oxatricyclo[6.3.1.04,12]dodecane-9,6'-3,4,5,7a-tetrahydro-2H-furo[2,3-b]pyran]-3-one

Details

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Internal ID 50bc44d3-29ae-424b-9402-35fb38cf737f
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbohydrates and carbohydrate conjugates > Glycosyl compounds > O-glycosyl compounds
IUPAC Name (1R,3'aS,4S,8S,9R,10R,12R)-2'-ethoxy-3',3'a-dihydroxy-4,8,10-trimethylspiro[2-oxatricyclo[6.3.1.04,12]dodecane-9,6'-3,4,5,7a-tetrahydro-2H-furo[2,3-b]pyran]-3-one
SMILES (Canonical) CCOC1C(C2(CCC3(C(CC4C5C3(CCCC5(C(=O)O4)C)C)C)OC2O1)O)O
SMILES (Isomeric) CCOC1C([C@]2(CC[C@]3([C@@H](C[C@@H]4[C@@H]5[C@@]3(CCC[C@@]5(C(=O)O4)C)C)C)OC2O1)O)O
InChI InChI=1S/C22H34O7/c1-5-26-16-15(23)21(25)9-10-22(29-18(21)28-16)12(2)11-13-14-19(3,17(24)27-13)7-6-8-20(14,22)4/h12-16,18,23,25H,5-11H2,1-4H3/t12-,13-,14+,15?,16?,18?,19+,20+,21+,22-/m1/s1
InChI Key ROLCCWPTXCTWNC-NVKDOJEFSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C22H34O7
Molecular Weight 410.50 g/mol
Exact Mass 410.23045342 g/mol
Topological Polar Surface Area (TPSA) 94.40 Ų
XlogP 2.10
Atomic LogP (AlogP) 2.12
H-Bond Acceptor 7
H-Bond Donor 2
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (1R,3'aS,4S,8S,9R,10R,12R)-2'-ethoxy-3',3'a-dihydroxy-4,8,10-trimethylspiro[2-oxatricyclo[6.3.1.04,12]dodecane-9,6'-3,4,5,7a-tetrahydro-2H-furo[2,3-b]pyran]-3-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9246 92.46%
Caco-2 + 0.5522 55.22%
Blood Brain Barrier - 0.7000 70.00%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Mitochondria 0.7753 77.53%
OATP2B1 inhibitior - 0.7255 72.55%
OATP1B1 inhibitior + 0.8723 87.23%
OATP1B3 inhibitior + 0.8878 88.78%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior + 0.7743 77.43%
P-glycoprotein inhibitior - 0.7093 70.93%
P-glycoprotein substrate - 0.6912 69.12%
CYP3A4 substrate + 0.6716 67.16%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8626 86.26%
CYP3A4 inhibition - 0.7776 77.76%
CYP2C9 inhibition - 0.8892 88.92%
CYP2C19 inhibition - 0.8795 87.95%
CYP2D6 inhibition - 0.9584 95.84%
CYP1A2 inhibition - 0.8747 87.47%
CYP2C8 inhibition - 0.6224 62.24%
CYP inhibitory promiscuity - 0.9442 94.42%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Non-required 0.6228 62.28%
Eye corrosion - 0.9930 99.30%
Eye irritation - 0.9602 96.02%
Skin irritation + 0.4924 49.24%
Skin corrosion - 0.9399 93.99%
Ames mutagenesis - 0.5500 55.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7106 71.06%
Micronuclear - 0.8800 88.00%
Hepatotoxicity + 0.5834 58.34%
skin sensitisation - 0.9326 93.26%
Respiratory toxicity + 0.6000 60.00%
Reproductive toxicity + 0.7444 74.44%
Mitochondrial toxicity + 0.7375 73.75%
Nephrotoxicity + 0.7998 79.98%
Acute Oral Toxicity (c) I 0.3957 39.57%
Estrogen receptor binding + 0.8407 84.07%
Androgen receptor binding + 0.6959 69.59%
Thyroid receptor binding + 0.6462 64.62%
Glucocorticoid receptor binding + 0.8377 83.77%
Aromatase binding + 0.8333 83.33%
PPAR gamma + 0.5743 57.43%
Honey bee toxicity - 0.7661 76.61%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity + 0.5100 51.00%
Fish aquatic toxicity + 0.9508 95.08%

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 95.48% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.21% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.89% 91.11%
CHEMBL3137262 O60341 LSD1/CoREST complex 90.47% 97.09%
CHEMBL218 P21554 Cannabinoid CB1 receptor 89.80% 96.61%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 89.71% 94.45%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.15% 86.33%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 85.45% 96.77%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 85.30% 85.14%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.13% 95.56%
CHEMBL2996 Q05655 Protein kinase C delta 83.25% 97.79%
CHEMBL1994 P08235 Mineralocorticoid receptor 83.18% 100.00%
CHEMBL2581 P07339 Cathepsin D 82.30% 98.95%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 82.28% 95.50%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 81.37% 94.00%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 80.41% 91.07%
CHEMBL4208 P20618 Proteasome component C5 80.05% 90.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.02% 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.
Marrubium globosum

Cross-Links

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PubChem 102597519
LOTUS LTS0191119
wikiData Q105242289