Clausenolide

Details

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Internal ID bf451c57-ffe5-4b37-aa76-c4b2f38de629
Taxonomy Lipids and lipid-like molecules > Steroids and steroid derivatives > Steroid lactones
IUPAC Name (1R,2R,4S,7S,8S,10S,12R,13S)-7-(furan-3-yl)-10,13-dihydroxy-1,8,12,13,15,15-hexamethyl-3,6,14-trioxapentacyclo[9.7.0.02,4.02,8.012,16]octadecane-5,18-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C25H32O8/c1-20(2)14-9-15(27)23(5)16(22(14,4)24(6,29)33-20)13(26)10-21(3)17(12-7-8-30-11-12)31-19(28)18-25(21,23)32-18/h7-8,11,13-14,16-18,26,29H,9-10H2,1-6H3/t13-,14?,16?,17-,18+,21-,22-,23+,24-,25+/m0/s1
InChI Key ABUJYLRTXBVIRH-KNFPJBQWSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C25H32O8
Molecular Weight 460.50 g/mol
Exact Mass 460.20971797 g/mol
Topological Polar Surface Area (TPSA) 119.00 Ų
XlogP 1.10
Atomic LogP (AlogP) 2.52
H-Bond Acceptor 8
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

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71899-58-6
DTXSID70420014
NSC294578

2D Structure

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2D Structure of Clausenolide

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9528 95.28%
Caco-2 - 0.6523 65.23%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Mitochondria 0.6138 61.38%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior - 0.3416 34.16%
OATP1B3 inhibitior + 0.8020 80.20%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior + 0.5672 56.72%
P-glycoprotein inhibitior - 0.4939 49.39%
P-glycoprotein substrate - 0.5486 54.86%
CYP3A4 substrate + 0.6514 65.14%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8434 84.34%
CYP3A4 inhibition + 0.6864 68.64%
CYP2C9 inhibition - 0.8210 82.10%
CYP2C19 inhibition - 0.8530 85.30%
CYP2D6 inhibition - 0.9244 92.44%
CYP1A2 inhibition - 0.8861 88.61%
CYP2C8 inhibition - 0.5797 57.97%
CYP inhibitory promiscuity - 0.9383 93.83%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.4367 43.67%
Eye corrosion - 0.9892 98.92%
Eye irritation - 0.9000 90.00%
Skin irritation - 0.6777 67.77%
Skin corrosion - 0.8677 86.77%
Ames mutagenesis - 0.5200 52.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4093 40.93%
Micronuclear - 0.6000 60.00%
Hepatotoxicity - 0.5551 55.51%
skin sensitisation - 0.8194 81.94%
Respiratory toxicity + 0.7556 75.56%
Reproductive toxicity + 0.8556 85.56%
Mitochondrial toxicity + 0.8500 85.00%
Nephrotoxicity + 0.6631 66.31%
Acute Oral Toxicity (c) I 0.4369 43.69%
Estrogen receptor binding + 0.8787 87.87%
Androgen receptor binding + 0.7878 78.78%
Thyroid receptor binding + 0.6571 65.71%
Glucocorticoid receptor binding + 0.7688 76.88%
Aromatase binding + 0.7924 79.24%
PPAR gamma + 0.6472 64.72%
Honey bee toxicity - 0.8410 84.10%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity + 0.5600 56.00%
Fish aquatic toxicity + 0.9557 95.57%

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 97.71% 91.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 97.34% 85.14%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.30% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 91.82% 97.09%
CHEMBL1806 P11388 DNA topoisomerase II alpha 88.54% 89.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 88.36% 99.23%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 87.71% 94.00%
CHEMBL2581 P07339 Cathepsin D 85.39% 98.95%
CHEMBL1994 P08235 Mineralocorticoid receptor 84.48% 100.00%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 84.23% 100.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.71% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 82.79% 95.56%
CHEMBL3038469 P24941 CDK2/Cyclin A 80.65% 91.38%

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.
Clausena anisata
Clausena excavata

Cross-Links

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PubChem 5458600
LOTUS LTS0025269
wikiData Q82231262