Citreohybriddione A

Details

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Internal ID 990753c0-3e14-4b81-842b-ce4842455253
Taxonomy Lipids and lipid-like molecules > Steroids and steroid derivatives > Steroid esters
IUPAC Name methyl (1R,5R,7S,9R,10S,12S,15S)-15-acetyloxy-7-hydroxy-4,5,7,10,14,14-hexamethyl-6,8,18-trioxo-19-oxapentacyclo[10.5.2.01,13.02,10.05,9]nonadec-3-ene-9-carboxylate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C28H36O9/c1-13-11-16-24(5,28(22(33)35-8)20(31)26(7,34)19(30)25(13,28)6)12-15-18-23(3,4)17(36-14(2)29)9-10-27(16,18)21(32)37-15/h11,15-18,34H,9-10,12H2,1-8H3/t15-,16?,17-,18?,24-,25-,26-,27+,28+/m0/s1
InChI Key NDCDPFWRTBREII-HEAQFLLASA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C28H36O9
Molecular Weight 516.60 g/mol
Exact Mass 516.23593272 g/mol
Topological Polar Surface Area (TPSA) 133.00 Ų
XlogP 2.40
Atomic LogP (AlogP) 2.32
H-Bond Acceptor 9
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Citreohybriddione A

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9873 98.73%
Caco-2 - 0.6646 66.46%
Blood Brain Barrier + 0.7000 70.00%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Mitochondria 0.7076 70.76%
OATP2B1 inhibitior - 0.8599 85.99%
OATP1B1 inhibitior + 0.8615 86.15%
OATP1B3 inhibitior + 0.8778 87.78%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.5750 57.50%
BSEP inhibitior + 0.8581 85.81%
P-glycoprotein inhibitior + 0.7142 71.42%
P-glycoprotein substrate - 0.6113 61.13%
CYP3A4 substrate + 0.7040 70.40%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8689 86.89%
CYP3A4 inhibition - 0.7505 75.05%
CYP2C9 inhibition - 0.7957 79.57%
CYP2C19 inhibition - 0.8214 82.14%
CYP2D6 inhibition - 0.9419 94.19%
CYP1A2 inhibition - 0.6390 63.90%
CYP2C8 inhibition + 0.4832 48.32%
CYP inhibitory promiscuity - 0.9313 93.13%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Non-required 0.5235 52.35%
Eye corrosion - 0.9907 99.07%
Eye irritation - 0.8793 87.93%
Skin irritation - 0.5732 57.32%
Skin corrosion - 0.8953 89.53%
Ames mutagenesis - 0.6070 60.70%
Human Ether-a-go-go-Related Gene inhibition - 0.5708 57.08%
Micronuclear - 0.7000 70.00%
Hepatotoxicity + 0.5158 51.58%
skin sensitisation - 0.7690 76.90%
Respiratory toxicity + 0.6000 60.00%
Reproductive toxicity + 0.8667 86.67%
Mitochondrial toxicity + 0.7500 75.00%
Nephrotoxicity + 0.6798 67.98%
Acute Oral Toxicity (c) III 0.3557 35.57%
Estrogen receptor binding + 0.8148 81.48%
Androgen receptor binding + 0.7282 72.82%
Thyroid receptor binding + 0.6772 67.72%
Glucocorticoid receptor binding + 0.7579 75.79%
Aromatase binding + 0.7538 75.38%
PPAR gamma + 0.6937 69.37%
Honey bee toxicity - 0.7050 70.50%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.5000 50.00%
Fish aquatic toxicity + 0.9773 97.73%

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 97.31% 85.14%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.22% 96.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 95.30% 94.45%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.33% 91.11%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 88.89% 97.14%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.02% 95.56%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 87.71% 99.23%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 84.90% 91.07%
CHEMBL3922 P50579 Methionine aminopeptidase 2 84.79% 97.28%
CHEMBL340 P08684 Cytochrome P450 3A4 84.19% 91.19%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 84.12% 94.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 83.42% 97.09%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 83.01% 93.03%
CHEMBL5966 P55899 IgG receptor FcRn large subunit p51 82.99% 90.93%
CHEMBL1994 P08235 Mineralocorticoid receptor 82.56% 100.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.63% 95.89%
CHEMBL5028 O14672 ADAM10 81.47% 97.50%

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.
There are no matching plants.

Cross-Links

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PubChem 139587133
LOTUS LTS0173068
wikiData Q77558805