Astraeusin K

Details

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Internal ID 7ef23620-15c1-4fd9-aace-9002b3ba4b94
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Triterpenoids
IUPAC Name (5R,10S,13R,14R,17R)-17-[(1S)-1-[(2S,5R,6R)-6-hydroxy-5-methyloxan-2-yl]ethyl]-4,4,10,13,14-pentamethyl-1,2,5,6,7,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-3-one
SMILES (Canonical) CC1CCC(OC1O)C(C)C2CCC3(C2(CCC4=C3CCC5C4(CCC(=O)C5(C)C)C)C)C
SMILES (Isomeric) C[C@@H]1CC[C@H](O[C@H]1O)[C@@H](C)[C@H]2CC[C@@]3([C@@]2(CCC4=C3CC[C@@H]5[C@@]4(CCC(=O)C5(C)C)C)C)C
InChI InChI=1S/C30H48O3/c1-18-8-10-23(33-26(18)32)19(2)20-12-16-30(7)22-9-11-24-27(3,4)25(31)14-15-28(24,5)21(22)13-17-29(20,30)6/h18-20,23-24,26,32H,8-17H2,1-7H3/t18-,19+,20-,23+,24+,26-,28-,29-,30+/m1/s1
InChI Key HYEBEDUHRUQRHO-DTFIVSTGSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C30H48O3
Molecular Weight 456.70 g/mol
Exact Mass 456.36034539 g/mol
Topological Polar Surface Area (TPSA) 46.50 Ų
XlogP 6.80
Atomic LogP (AlogP) 7.07
H-Bond Acceptor 3
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 Astraeusin K

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9934 99.34%
Caco-2 + 0.5891 58.91%
Blood Brain Barrier - 0.6500 65.00%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Mitochondria 0.7982 79.82%
OATP2B1 inhibitior - 0.7120 71.20%
OATP1B1 inhibitior + 0.8374 83.74%
OATP1B3 inhibitior + 0.9326 93.26%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior + 0.5750 57.50%
BSEP inhibitior + 0.5910 59.10%
P-glycoprotein inhibitior - 0.5083 50.83%
P-glycoprotein substrate - 0.6633 66.33%
CYP3A4 substrate + 0.6614 66.14%
CYP2C9 substrate - 0.8028 80.28%
CYP2D6 substrate - 0.8224 82.24%
CYP3A4 inhibition - 0.7980 79.80%
CYP2C9 inhibition - 0.8682 86.82%
CYP2C19 inhibition - 0.7945 79.45%
CYP2D6 inhibition - 0.9421 94.21%
CYP1A2 inhibition - 0.7365 73.65%
CYP2C8 inhibition + 0.5057 50.57%
CYP inhibitory promiscuity - 0.8978 89.78%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.6066 60.66%
Eye corrosion - 0.9938 99.38%
Eye irritation - 0.9485 94.85%
Skin irritation + 0.5916 59.16%
Skin corrosion - 0.9350 93.50%
Ames mutagenesis - 0.5700 57.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3761 37.61%
Micronuclear - 0.8300 83.00%
Hepatotoxicity - 0.5750 57.50%
skin sensitisation - 0.5976 59.76%
Respiratory toxicity + 0.6111 61.11%
Reproductive toxicity + 0.9444 94.44%
Mitochondrial toxicity + 0.8375 83.75%
Nephrotoxicity + 0.6839 68.39%
Acute Oral Toxicity (c) III 0.6253 62.53%
Estrogen receptor binding + 0.7613 76.13%
Androgen receptor binding + 0.7365 73.65%
Thyroid receptor binding + 0.7251 72.51%
Glucocorticoid receptor binding + 0.8352 83.52%
Aromatase binding + 0.7125 71.25%
PPAR gamma + 0.5726 57.26%
Honey bee toxicity - 0.8226 82.26%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity - 0.6300 63.00%
Fish aquatic toxicity + 0.9892 98.92%

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
CHEMBL2581 P07339 Cathepsin D 95.04% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 91.92% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.54% 96.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 86.95% 100.00%
CHEMBL4685 P14902 Indoleamine 2,3-dioxygenase 86.83% 96.38%
CHEMBL1951 P21397 Monoamine oxidase A 86.36% 91.49%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.28% 95.56%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 85.95% 99.23%
CHEMBL2842 P42345 Serine/threonine-protein kinase mTOR 85.58% 92.78%
CHEMBL3137262 O60341 LSD1/CoREST complex 85.51% 97.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.85% 86.33%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 83.82% 96.77%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 82.55% 82.69%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 81.96% 90.71%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 81.78% 93.04%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 81.78% 85.14%
CHEMBL2140 P48775 Tryptophan 2,3-dioxygenase 81.30% 98.46%
CHEMBL2553 Q15418 Ribosomal protein S6 kinase alpha 1 80.95% 85.11%
CHEMBL1795139 Q8IU80 Transmembrane protease serine 6 80.65% 98.33%

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 139585847
LOTUS LTS0033812
wikiData Q77493156