CID 21770763

Details

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Internal ID 4dd40c1f-9a83-4fab-93d0-86cd5ed6f194
Taxonomy Organoheterocyclic compounds > Oxanes
IUPAC Name [(1R,2R,4R,6S,9R,13S,14R)-2-hydroxy-5,5,9-trimethyl-17-methylidene-10,16-dioxo-15-oxatetracyclo[11.2.2.01,14.04,9]heptadecan-6-yl] acetate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C22H30O6/c1-11-13-6-7-15(24)21(5)9-8-17(27-12(2)23)20(3,4)14(21)10-16(25)22(18(11)26)19(13)28-22/h13-14,16-17,19,25H,1,6-10H2,2-5H3/t13-,14+,16+,17-,19+,21+,22-/m0/s1
InChI Key ZQKZJBMQBWMNHT-WPFJWBHQSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C22H30O6
Molecular Weight 390.50 g/mol
Exact Mass 390.20423867 g/mol
Topological Polar Surface Area (TPSA) 93.20 Ų
XlogP 1.90
Atomic LogP (AlogP) 2.37
H-Bond Acceptor 6
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of CID 21770763

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9766 97.66%
Caco-2 - 0.6188 61.88%
Blood Brain Barrier + 0.6750 67.50%
Human oral bioavailability - 0.6571 65.71%
Subcellular localzation Mitochondria 0.6981 69.81%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8671 86.71%
OATP1B3 inhibitior + 0.8842 88.42%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior - 0.8534 85.34%
P-glycoprotein inhibitior - 0.5721 57.21%
P-glycoprotein substrate - 0.8205 82.05%
CYP3A4 substrate + 0.6885 68.85%
CYP2C9 substrate - 0.8149 81.49%
CYP2D6 substrate - 0.8717 87.17%
CYP3A4 inhibition - 0.5095 50.95%
CYP2C9 inhibition - 0.8124 81.24%
CYP2C19 inhibition - 0.8419 84.19%
CYP2D6 inhibition - 0.9412 94.12%
CYP1A2 inhibition - 0.7047 70.47%
CYP2C8 inhibition + 0.5631 56.31%
CYP inhibitory promiscuity - 0.9631 96.31%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.6688 66.88%
Eye corrosion - 0.9893 98.93%
Eye irritation - 0.8844 88.44%
Skin irritation + 0.5318 53.18%
Skin corrosion - 0.9105 91.05%
Ames mutagenesis - 0.7600 76.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7453 74.53%
Micronuclear - 0.5800 58.00%
Hepatotoxicity - 0.5092 50.92%
skin sensitisation - 0.7348 73.48%
Respiratory toxicity + 0.5889 58.89%
Reproductive toxicity + 0.9000 90.00%
Mitochondrial toxicity + 0.8375 83.75%
Nephrotoxicity + 0.5778 57.78%
Acute Oral Toxicity (c) I 0.3698 36.98%
Estrogen receptor binding + 0.8176 81.76%
Androgen receptor binding + 0.6449 64.49%
Thyroid receptor binding + 0.6149 61.49%
Glucocorticoid receptor binding + 0.7496 74.96%
Aromatase binding + 0.6446 64.46%
PPAR gamma + 0.5943 59.43%
Honey bee toxicity - 0.7424 74.24%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity - 0.5100 51.00%
Fish aquatic toxicity + 0.9913 99.13%

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 94.19% 91.11%
CHEMBL241 Q14432 Phosphodiesterase 3A 91.27% 92.94%
CHEMBL3137262 O60341 LSD1/CoREST complex 91.20% 97.09%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 90.11% 99.23%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.71% 96.09%
CHEMBL340 P08684 Cytochrome P450 3A4 89.55% 91.19%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 89.07% 85.14%
CHEMBL1994 P08235 Mineralocorticoid receptor 88.35% 100.00%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 88.04% 93.04%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 87.19% 92.62%
CHEMBL4681 P42330 Aldo-keto-reductase family 1 member C3 83.96% 89.05%
CHEMBL1907602 P06493 Cyclin-dependent kinase 1/cyclin B1 83.81% 91.24%
CHEMBL259 P32245 Melanocortin receptor 4 83.80% 95.38%
CHEMBL1871 P10275 Androgen Receptor 83.74% 96.43%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 83.55% 94.45%
CHEMBL2581 P07339 Cathepsin D 82.66% 98.95%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 82.54% 82.69%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 82.49% 94.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 82.15% 95.56%
CHEMBL253 P34972 Cannabinoid CB2 receptor 80.15% 97.25%
CHEMBL1806 P11388 DNA topoisomerase II alpha 80.07% 89.00%
CHEMBL2996 Q05655 Protein kinase C delta 80.06% 97.79%

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.
Isodon shikokianus

Cross-Links

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PubChem 21770763
LOTUS LTS0270553
wikiData Q105381507