Ergost-24(28)-ene-3beta,5alpha,6beta,7beta-tetrol

Details

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Internal ID b6206f96-de8e-4414-bcc6-1674ef10a8f7
Taxonomy Lipids and lipid-like molecules > Steroids and steroid derivatives > Ergostane steroids > Ergosterols and derivatives
IUPAC Name (3S,5R,6R,7R,8S,9S,10R,13R,14S,17R)-10,13-dimethyl-17-[(2R)-6-methyl-5-methylideneheptan-2-yl]-1,2,3,4,6,7,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthrene-3,5,6,7-tetrol
SMILES (Canonical) CC(C)C(=C)CCC(C)C1CCC2C1(CCC3C2C(C(C4(C3(CCC(C4)O)C)O)O)O)C
SMILES (Isomeric) C[C@H](CCC(=C)C(C)C)[C@H]1CC[C@@H]2[C@@]1(CC[C@H]3[C@H]2[C@H]([C@H]([C@@]4([C@@]3(CC[C@@H](C4)O)C)O)O)O)C
InChI InChI=1S/C28H48O4/c1-16(2)17(3)7-8-18(4)20-9-10-21-23-22(12-13-26(20,21)5)27(6)14-11-19(29)15-28(27,32)25(31)24(23)30/h16,18-25,29-32H,3,7-15H2,1-2,4-6H3/t18-,19+,20-,21+,22+,23+,24-,25-,26-,27-,28+/m1/s1
InChI Key CSEIKYIGVBFUKD-MISHLHQHSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C28H48O4
Molecular Weight 448.70 g/mol
Exact Mass 448.35526001 g/mol
Topological Polar Surface Area (TPSA) 80.90 Ų
XlogP 6.10
Atomic LogP (AlogP) 4.69
H-Bond Acceptor 4
H-Bond Donor 4
Rotatable Bonds 5

Synonyms

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BDBM50241893
ergost-24(28)-ene-3-beta,5-alpha,6-beta,7-beta-tetrol

2D Structure

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2D Structure of Ergost-24(28)-ene-3beta,5alpha,6beta,7beta-tetrol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9732 97.32%
Caco-2 - 0.7210 72.10%
Blood Brain Barrier + 0.7750 77.50%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.4932 49.32%
OATP2B1 inhibitior - 0.5787 57.87%
OATP1B1 inhibitior + 0.8692 86.92%
OATP1B3 inhibitior + 0.8556 85.56%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior + 0.6598 65.98%
P-glycoprotein inhibitior - 0.6165 61.65%
P-glycoprotein substrate + 0.5000 50.00%
CYP3A4 substrate + 0.7095 70.95%
CYP2C9 substrate - 0.5858 58.58%
CYP2D6 substrate - 0.7545 75.45%
CYP3A4 inhibition - 0.8538 85.38%
CYP2C9 inhibition - 0.8304 83.04%
CYP2C19 inhibition - 0.7307 73.07%
CYP2D6 inhibition - 0.9446 94.46%
CYP1A2 inhibition - 0.8908 89.08%
CYP2C8 inhibition - 0.7035 70.35%
CYP inhibitory promiscuity - 0.8609 86.09%
UGT catelyzed + 1.0000 100.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.7056 70.56%
Eye corrosion - 0.9916 99.16%
Eye irritation - 0.9402 94.02%
Skin irritation + 0.5569 55.69%
Skin corrosion - 0.9320 93.20%
Ames mutagenesis - 0.5000 50.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6675 66.75%
Micronuclear - 0.9400 94.00%
Hepatotoxicity - 0.5313 53.13%
skin sensitisation - 0.7244 72.44%
Respiratory toxicity + 0.7333 73.33%
Reproductive toxicity + 0.9444 94.44%
Mitochondrial toxicity + 0.9625 96.25%
Nephrotoxicity - 0.7981 79.81%
Acute Oral Toxicity (c) I 0.7612 76.12%
Estrogen receptor binding + 0.6575 65.75%
Androgen receptor binding + 0.7616 76.16%
Thyroid receptor binding + 0.6455 64.55%
Glucocorticoid receptor binding + 0.7017 70.17%
Aromatase binding + 0.6275 62.75%
PPAR gamma + 0.5500 55.00%
Honey bee toxicity - 0.7496 74.96%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.5400 54.00%
Fish aquatic toxicity + 0.9930 99.30%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
CHEMBL2808 Q13133 LXR-alpha 170 nM
170 nM
EC50
EC50
via Super-PRED
PMID: 16124770

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL253 P34972 Cannabinoid CB2 receptor 99.09% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.95% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.15% 91.11%
CHEMBL221 P23219 Cyclooxygenase-1 94.73% 90.17%
CHEMBL3137262 O60341 LSD1/CoREST complex 92.11% 97.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 91.37% 100.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 91.25% 94.45%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 90.07% 95.89%
CHEMBL226 P30542 Adenosine A1 receptor 90.04% 95.93%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 89.55% 82.69%
CHEMBL2581 P07339 Cathepsin D 88.72% 98.95%
CHEMBL1871 P10275 Androgen Receptor 86.83% 96.43%
CHEMBL5608 Q16288 NT-3 growth factor receptor 86.57% 95.89%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 84.60% 92.62%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 84.20% 90.71%
CHEMBL4227 P25090 Lipoxin A4 receptor 82.52% 100.00%
CHEMBL4681 P42330 Aldo-keto-reductase family 1 member C3 82.48% 89.05%
CHEMBL2094135 Q96BI3 Gamma-secretase 82.13% 98.05%
CHEMBL2179 P04062 Beta-glucocerebrosidase 82.12% 85.31%
CHEMBL218 P21554 Cannabinoid CB1 receptor 81.55% 96.61%
CHEMBL3746 P80365 11-beta-hydroxysteroid dehydrogenase 2 80.43% 94.78%
CHEMBL2959 Q08881 Tyrosine-protein kinase ITK/TSK 80.39% 95.00%
CHEMBL240 Q12809 HERG 80.32% 89.76%

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.
Ageratina sternbergiana
Astragalus sevangensis
Citrus × aurantium
Cleome dodecandra
Elsholtzia blanda
Prunus tomentosa

Cross-Links

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PubChem 11037703
NPASS NPC216420
ChEMBL CHEMBL520370
LOTUS LTS0098948
wikiData Q104969124