3beta-Acetoxyclerodinin C

Details

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Internal ID 05d01469-636b-4b11-9346-55b747a36963
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Tricarboxylic acids and derivatives
IUPAC Name [(3S,4R,4aR,5S,7R,8S,8aR)-8-[(2S,3aS,5R,6aR)-5-ethoxy-2,3,3a,4,5,6a-hexahydrofuro[2,3-b]furan-2-yl]-3,5-diacetyloxy-7,8-dimethylspiro[2,3,5,6,7,8a-hexahydro-1H-naphthalene-4,2'-oxirane]-4a-yl]methyl acetate
SMILES (Canonical) CCOC1CC2CC(OC2O1)C3(C(CC(C4(C3CCC(C45CO5)OC(=O)C)COC(=O)C)OC(=O)C)C)C
SMILES (Isomeric) CCO[C@H]1C[C@@H]2C[C@H](O[C@@H]2O1)[C@]3([C@@H](C[C@@H]([C@@]4([C@@H]3CC[C@@H]([C@]45CO5)OC(=O)C)COC(=O)C)OC(=O)C)C)C
InChI InChI=1S/C28H42O10/c1-7-32-24-12-19-11-22(37-25(19)38-24)26(6)15(2)10-23(36-18(5)31)27(13-33-16(3)29)20(26)8-9-21(35-17(4)30)28(27)14-34-28/h15,19-25H,7-14H2,1-6H3/t15-,19+,20-,21+,22+,23+,24-,25-,26+,27+,28-/m1/s1
InChI Key KELWGSSLXXIRKR-ANBJSBCDSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C28H42O10
Molecular Weight 538.60 g/mol
Exact Mass 538.27779753 g/mol
Topological Polar Surface Area (TPSA) 119.00 Ų
XlogP 2.80
Atomic LogP (AlogP) 3.14
H-Bond Acceptor 10
H-Bond Donor 0
Rotatable Bonds 7

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 3beta-Acetoxyclerodinin C

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9845 98.45%
Caco-2 - 0.7111 71.11%
Blood Brain Barrier + 0.8250 82.50%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Mitochondria 0.7552 75.52%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8742 87.42%
OATP1B3 inhibitior + 0.9669 96.69%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.6500 65.00%
BSEP inhibitior + 0.8914 89.14%
P-glycoprotein inhibitior + 0.7352 73.52%
P-glycoprotein substrate + 0.5419 54.19%
CYP3A4 substrate + 0.6961 69.61%
CYP2C9 substrate - 0.8146 81.46%
CYP2D6 substrate - 0.8690 86.90%
CYP3A4 inhibition - 0.6551 65.51%
CYP2C9 inhibition - 0.7559 75.59%
CYP2C19 inhibition - 0.7020 70.20%
CYP2D6 inhibition - 0.9455 94.55%
CYP1A2 inhibition - 0.8946 89.46%
CYP2C8 inhibition + 0.6705 67.05%
CYP inhibitory promiscuity - 0.7752 77.52%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.5455 54.55%
Eye corrosion - 0.9849 98.49%
Eye irritation - 0.8923 89.23%
Skin irritation - 0.7253 72.53%
Skin corrosion - 0.9274 92.74%
Ames mutagenesis - 0.6500 65.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4227 42.27%
Micronuclear - 0.5600 56.00%
Hepatotoxicity - 0.5483 54.83%
skin sensitisation - 0.9046 90.46%
Respiratory toxicity - 0.7667 76.67%
Reproductive toxicity + 0.6667 66.67%
Mitochondrial toxicity + 0.5125 51.25%
Nephrotoxicity + 0.7406 74.06%
Acute Oral Toxicity (c) III 0.4250 42.50%
Estrogen receptor binding + 0.8548 85.48%
Androgen receptor binding + 0.6617 66.17%
Thyroid receptor binding - 0.5409 54.09%
Glucocorticoid receptor binding + 0.7016 70.16%
Aromatase binding + 0.7226 72.26%
PPAR gamma + 0.7467 74.67%
Honey bee toxicity - 0.7626 76.26%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.5587 55.87%
Fish aquatic toxicity + 0.9869 98.69%

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 98.79% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 93.51% 97.25%
CHEMBL3137262 O60341 LSD1/CoREST complex 93.20% 97.09%
CHEMBL2581 P07339 Cathepsin D 92.75% 98.95%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 92.10% 85.14%
CHEMBL4681 P42330 Aldo-keto-reductase family 1 member C3 91.40% 89.05%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 90.68% 96.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 90.29% 94.45%
CHEMBL3267 P48736 PI3-kinase p110-gamma subunit 89.70% 95.71%
CHEMBL340 P08684 Cytochrome P450 3A4 89.59% 91.19%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.16% 91.11%
CHEMBL5255 O00206 Toll-like receptor 4 88.74% 92.50%
CHEMBL3922 P50579 Methionine aminopeptidase 2 88.66% 97.28%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 87.69% 94.33%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 87.57% 92.62%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 87.53% 96.77%
CHEMBL241 Q14432 Phosphodiesterase 3A 86.27% 92.94%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.24% 86.33%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 84.15% 100.00%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 83.27% 97.14%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 82.60% 95.50%
CHEMBL1907601 P11802 Cyclin-dependent kinase 4/cyclin D1 81.94% 98.99%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 80.96% 82.69%
CHEMBL1806 P11388 DNA topoisomerase II alpha 80.53% 89.00%
CHEMBL2413 P32246 C-C chemokine receptor type 1 80.24% 89.50%

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.
Ajuga parviflora

Cross-Links

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PubChem 102247114
LOTUS LTS0105257
wikiData Q105140032