3beta-Hydroxy-1,11-dioxo-ergosta-8,24(28)-diene-4alpha-carboxylic acid

Details

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Internal ID 0c23c487-b21c-40ec-8885-828d596a75c6
Taxonomy Lipids and lipid-like molecules > Steroids and steroid derivatives > Ergostane steroids > Ergosterols and derivatives
IUPAC Name (3S,4S,5S,10S,13R,14R,17R)-3-hydroxy-10,13-dimethyl-17-[(2R)-6-methyl-5-methylideneheptan-2-yl]-1,11-dioxo-3,4,5,6,7,12,14,15,16,17-decahydro-2H-cyclopenta[a]phenanthrene-4-carboxylic acid
SMILES (Canonical) CC(C)C(=C)CCC(C)C1CCC2C1(CC(=O)C3=C2CCC4C3(C(=O)CC(C4C(=O)O)O)C)C
SMILES (Isomeric) C[C@H](CCC(=C)C(C)C)[C@H]1CC[C@@H]2[C@@]1(CC(=O)C3=C2CC[C@@H]4[C@@]3(C(=O)C[C@@H]([C@H]4C(=O)O)O)C)C
InChI InChI=1S/C29H42O5/c1-15(2)16(3)7-8-17(4)19-11-12-20-18-9-10-21-25(27(33)34)22(30)13-24(32)29(21,6)26(18)23(31)14-28(19,20)5/h15,17,19-22,25,30H,3,7-14H2,1-2,4-6H3,(H,33,34)/t17-,19-,20+,21+,22+,25+,28-,29-/m1/s1
InChI Key MCQNBADNXHETRN-IIDSXYMRSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C29H42O5
Molecular Weight 470.60 g/mol
Exact Mass 470.30322444 g/mol
Topological Polar Surface Area (TPSA) 91.70 Ų
XlogP 5.60
Atomic LogP (AlogP) 5.37
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 6

Synonyms

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1,11-Dioxo-3beta-hydroxy-5alpha-ergosta-8,24(28)-diene-4alpha-carboxylic acid

2D Structure

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2D Structure of 3beta-Hydroxy-1,11-dioxo-ergosta-8,24(28)-diene-4alpha-carboxylic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9798 97.98%
Caco-2 - 0.5463 54.63%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Mitochondria 0.7264 72.64%
OATP2B1 inhibitior - 0.5710 57.10%
OATP1B1 inhibitior + 0.8604 86.04%
OATP1B3 inhibitior - 0.3972 39.72%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior + 0.8840 88.40%
P-glycoprotein inhibitior + 0.6201 62.01%
P-glycoprotein substrate - 0.5521 55.21%
CYP3A4 substrate + 0.6667 66.67%
CYP2C9 substrate - 0.7735 77.35%
CYP2D6 substrate - 0.9031 90.31%
CYP3A4 inhibition - 0.7567 75.67%
CYP2C9 inhibition - 0.8978 89.78%
CYP2C19 inhibition - 0.9374 93.74%
CYP2D6 inhibition - 0.9566 95.66%
CYP1A2 inhibition - 0.8973 89.73%
CYP2C8 inhibition - 0.6901 69.01%
CYP inhibitory promiscuity - 0.8825 88.25%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.6812 68.12%
Eye corrosion - 0.9929 99.29%
Eye irritation - 0.9322 93.22%
Skin irritation + 0.7003 70.03%
Skin corrosion - 0.9346 93.46%
Ames mutagenesis - 0.7154 71.54%
Human Ether-a-go-go-Related Gene inhibition - 0.5000 50.00%
Micronuclear - 0.7700 77.00%
Hepatotoxicity + 0.5327 53.27%
skin sensitisation - 0.7457 74.57%
Respiratory toxicity + 0.7778 77.78%
Reproductive toxicity + 0.9333 93.33%
Mitochondrial toxicity + 0.9750 97.50%
Nephrotoxicity + 0.4624 46.24%
Acute Oral Toxicity (c) I 0.8672 86.72%
Estrogen receptor binding + 0.7155 71.55%
Androgen receptor binding + 0.7436 74.36%
Thyroid receptor binding + 0.6010 60.10%
Glucocorticoid receptor binding + 0.7632 76.32%
Aromatase binding + 0.5519 55.19%
PPAR gamma + 0.5667 56.67%
Honey bee toxicity - 0.8004 80.04%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.6800 68.00%
Fish aquatic toxicity + 1.0000 100.00%

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 97.86% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.09% 96.09%
CHEMBL2581 P07339 Cathepsin D 96.54% 98.95%
CHEMBL253 P34972 Cannabinoid CB2 receptor 94.40% 97.25%
CHEMBL221 P23219 Cyclooxygenase-1 93.58% 90.17%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 90.38% 93.04%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 90.15% 93.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 88.64% 99.23%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 88.51% 90.71%
CHEMBL3137262 O60341 LSD1/CoREST complex 88.47% 97.09%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 87.18% 92.62%
CHEMBL340 P08684 Cytochrome P450 3A4 85.65% 91.19%
CHEMBL2996 Q05655 Protein kinase C delta 85.63% 97.79%
CHEMBL2001 Q9H244 Purinergic receptor P2Y12 84.42% 96.00%
CHEMBL2553 Q15418 Ribosomal protein S6 kinase alpha 1 83.80% 85.11%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 83.50% 95.89%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.12% 95.56%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 83.01% 85.14%
CHEMBL299 P17252 Protein kinase C alpha 81.81% 98.03%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 81.60% 96.47%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 80.97% 95.50%
CHEMBL3359 P21462 Formyl peptide receptor 1 80.68% 93.56%
CHEMBL4227 P25090 Lipoxin A4 receptor 80.49% 100.00%
CHEMBL2959 Q08881 Tyrosine-protein kinase ITK/TSK 80.10% 95.00%

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.
Medicago sativa
Pseudostellaria heterophylla

Cross-Links

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PubChem 9982179
NPASS NPC208448
LOTUS LTS0063847
wikiData Q77310788