Citreohybridone L

Details

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Internal ID 81efabb0-3709-4eaa-8bd8-24534167fd34
Taxonomy Lipids and lipid-like molecules > Steroids and steroid derivatives > Steroid esters
IUPAC Name [(1S,2S,5R,6R,7S,8S,9R,10R,12S,15S)-6,15-diacetyloxy-7-hydroxy-4,5,7,10,14,14-hexamethyl-18-oxo-19,20-dioxahexacyclo[10.5.2.12,8.01,13.02,10.05,9]icos-3-en-9-yl]methyl acetate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C31H42O10/c1-15-12-31-26(7,13-19-21-25(5,6)20(38-17(3)33)10-11-29(21,31)24(35)40-19)30(14-37-16(2)32)23(41-31)28(9,36)22(27(15,30)8)39-18(4)34/h12,19-23,36H,10-11,13-14H2,1-9H3/t19-,20-,21?,22+,23+,26+,27-,28+,29+,30-,31-/m0/s1
InChI Key BPRFRXZPTGBRDQ-BRUATXQLSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C31H42O10
Molecular Weight 574.70 g/mol
Exact Mass 574.27779753 g/mol
Topological Polar Surface Area (TPSA) 135.00 Ų
XlogP 2.20
Atomic LogP (AlogP) 3.03
H-Bond Acceptor 10
H-Bond Donor 1
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Citreohybridone L

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9759 97.59%
Caco-2 - 0.7451 74.51%
Blood Brain Barrier + 0.8000 80.00%
Human oral bioavailability - 0.7857 78.57%
Subcellular localzation Mitochondria 0.8554 85.54%
OATP2B1 inhibitior - 0.8606 86.06%
OATP1B1 inhibitior + 0.8390 83.90%
OATP1B3 inhibitior + 0.8634 86.34%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior + 0.6000 60.00%
BSEP inhibitior + 0.9675 96.75%
P-glycoprotein inhibitior + 0.7814 78.14%
P-glycoprotein substrate - 0.5212 52.12%
CYP3A4 substrate + 0.7159 71.59%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8698 86.98%
CYP3A4 inhibition - 0.8465 84.65%
CYP2C9 inhibition - 0.6481 64.81%
CYP2C19 inhibition - 0.8642 86.42%
CYP2D6 inhibition - 0.9405 94.05%
CYP1A2 inhibition - 0.7841 78.41%
CYP2C8 inhibition + 0.5893 58.93%
CYP inhibitory promiscuity - 0.8433 84.33%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.4721 47.21%
Eye corrosion - 0.9909 99.09%
Eye irritation - 0.8744 87.44%
Skin irritation + 0.5255 52.55%
Skin corrosion - 0.9388 93.88%
Ames mutagenesis - 0.6770 67.70%
Human Ether-a-go-go-Related Gene inhibition - 0.6147 61.47%
Micronuclear - 0.7700 77.00%
Hepatotoxicity + 0.5246 52.46%
skin sensitisation - 0.8762 87.62%
Respiratory toxicity + 0.5333 53.33%
Reproductive toxicity + 0.8889 88.89%
Mitochondrial toxicity + 0.6250 62.50%
Nephrotoxicity + 0.7501 75.01%
Acute Oral Toxicity (c) III 0.4315 43.15%
Estrogen receptor binding + 0.7905 79.05%
Androgen receptor binding + 0.7713 77.13%
Thyroid receptor binding + 0.6135 61.35%
Glucocorticoid receptor binding + 0.7891 78.91%
Aromatase binding + 0.7569 75.69%
PPAR gamma + 0.7392 73.92%
Honey bee toxicity - 0.7517 75.17%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity + 0.5350 53.50%
Fish aquatic toxicity + 0.9944 99.44%

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
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 97.91% 85.14%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.65% 96.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 94.58% 94.45%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.52% 91.11%
CHEMBL3922 P50579 Methionine aminopeptidase 2 93.31% 97.28%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 93.19% 94.80%
CHEMBL1806 P11388 DNA topoisomerase II alpha 92.70% 89.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 90.91% 97.09%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 87.95% 99.23%
CHEMBL1994 P08235 Mineralocorticoid receptor 86.80% 100.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 85.58% 95.89%
CHEMBL1937 Q92769 Histone deacetylase 2 85.06% 94.75%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.08% 95.56%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 83.84% 94.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.16% 86.33%
CHEMBL340 P08684 Cytochrome P450 3A4 82.82% 91.19%
CHEMBL241 Q14432 Phosphodiesterase 3A 82.20% 92.94%
CHEMBL5028 O14672 ADAM10 80.75% 97.50%
CHEMBL5255 O00206 Toll-like receptor 4 80.64% 92.50%
CHEMBL1871 P10275 Androgen Receptor 80.04% 96.43%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 139583918
LOTUS LTS0133421
wikiData Q75069206