(3'R,4R,5R,6R,8S,10R,12R)-3',4,6,12,17,17-hexamethylspiro[9,18,24-trioxapentacyclo[19.2.1.04,12.05,10.016,22]tetracosa-15,20,22-triene-8,5'-oxolane]-2',19-dione

Details

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Internal ID 13101ec4-a3a7-4949-a5e0-278fa2b20165
Taxonomy Organic oxygen compounds > Organooxygen compounds > Ethers > Acetals > Ketals
IUPAC Name (3'R,4R,5R,6R,8S,10R,12R)-3',4,6,12,17,17-hexamethylspiro[9,18,24-trioxapentacyclo[19.2.1.04,12.05,10.016,22]tetracosa-15,20,22-triene-8,5'-oxolane]-2',19-dione
SMILES (Canonical) CC1CC2(CC(C(=O)O2)C)OC3C1C4(CCC5C=C6C(=CCCC4(C3)C)C(OC(=O)C=C6O5)(C)C)C
SMILES (Isomeric) C[C@@H]1C[C@]2(C[C@H](C(=O)O2)C)O[C@H]3[C@H]1[C@]4(CCC5C=C6C(=CCC[C@@]4(C3)C)C(OC(=O)C=C6O5)(C)C)C
InChI InChI=1S/C30H40O6/c1-17-14-30(15-18(2)26(32)36-30)34-23-16-28(5)10-7-8-21-20-12-19(9-11-29(28,6)25(17)23)33-22(20)13-24(31)35-27(21,3)4/h8,12-13,17-19,23,25H,7,9-11,14-16H2,1-6H3/t17-,18-,19?,23-,25+,28-,29-,30+/m1/s1
InChI Key IUGWEDGNVVMLTL-XWKQTQCQSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C30H40O6
Molecular Weight 496.60 g/mol
Exact Mass 496.28248899 g/mol
Topological Polar Surface Area (TPSA) 71.10 Ų
XlogP 5.10
Atomic LogP (AlogP) 5.77
H-Bond Acceptor 6
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (3'R,4R,5R,6R,8S,10R,12R)-3',4,6,12,17,17-hexamethylspiro[9,18,24-trioxapentacyclo[19.2.1.04,12.05,10.016,22]tetracosa-15,20,22-triene-8,5'-oxolane]-2',19-dione

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9878 98.78%
Caco-2 - 0.5482 54.82%
Blood Brain Barrier + 0.7750 77.50%
Human oral bioavailability + 0.5429 54.29%
Subcellular localzation Mitochondria 0.7830 78.30%
OATP2B1 inhibitior - 0.8619 86.19%
OATP1B1 inhibitior + 0.8303 83.03%
OATP1B3 inhibitior + 0.9534 95.34%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior + 0.5500 55.00%
BSEP inhibitior + 0.9460 94.60%
P-glycoprotein inhibitior + 0.8479 84.79%
P-glycoprotein substrate + 0.5120 51.20%
CYP3A4 substrate + 0.6965 69.65%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8714 87.14%
CYP3A4 inhibition - 0.7980 79.80%
CYP2C9 inhibition - 0.8752 87.52%
CYP2C19 inhibition - 0.9215 92.15%
CYP2D6 inhibition - 0.9496 94.96%
CYP1A2 inhibition - 0.5888 58.88%
CYP2C8 inhibition + 0.6686 66.86%
CYP inhibitory promiscuity - 0.9517 95.17%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9200 92.00%
Carcinogenicity (trinary) Non-required 0.5733 57.33%
Eye corrosion - 0.9834 98.34%
Eye irritation - 0.9403 94.03%
Skin irritation + 0.5161 51.61%
Skin corrosion - 0.8059 80.59%
Ames mutagenesis - 0.6300 63.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8365 83.65%
Micronuclear - 0.7900 79.00%
Hepatotoxicity + 0.5543 55.43%
skin sensitisation - 0.7219 72.19%
Respiratory toxicity + 0.7222 72.22%
Reproductive toxicity + 0.6333 63.33%
Mitochondrial toxicity + 0.7875 78.75%
Nephrotoxicity + 0.5210 52.10%
Acute Oral Toxicity (c) III 0.4340 43.40%
Estrogen receptor binding + 0.8031 80.31%
Androgen receptor binding + 0.7571 75.71%
Thyroid receptor binding + 0.6785 67.85%
Glucocorticoid receptor binding + 0.8483 84.83%
Aromatase binding + 0.8038 80.38%
PPAR gamma + 0.6643 66.43%
Honey bee toxicity - 0.7327 73.27%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity + 0.7400 74.00%
Fish aquatic toxicity + 0.9893 98.93%

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 96.08% 91.11%
CHEMBL253 P34972 Cannabinoid CB2 receptor 94.92% 97.25%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.92% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.64% 96.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 90.52% 100.00%
CHEMBL1871 P10275 Androgen Receptor 89.13% 96.43%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 87.76% 94.80%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.70% 86.33%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 86.20% 85.94%
CHEMBL3137262 O60341 LSD1/CoREST complex 85.96% 97.09%
CHEMBL1806 P11388 DNA topoisomerase II alpha 85.89% 89.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 85.32% 95.89%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 84.92% 86.00%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 81.88% 96.77%
CHEMBL3746 P80365 11-beta-hydroxysteroid dehydrogenase 2 80.80% 94.78%
CHEMBL230 P35354 Cyclooxygenase-2 80.30% 89.63%
CHEMBL218 P21554 Cannabinoid CB1 receptor 80.25% 96.61%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 80.07% 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.
Pseudolarix amabilis

Cross-Links

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PubChem 101244786
LOTUS LTS0243187
wikiData Q105120551