Acnistin G

Details

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Internal ID dac8558d-0d33-4b7b-8901-ba94fd288328
Taxonomy Lipids and lipid-like molecules > Steroids and steroid derivatives > Steroid lactones
IUPAC Name (1S,2R,7S,9R,11S,12S,15R,16S)-15-hydroxy-15-[(1R,4R,5R,7S)-4-hydroxy-4,5-dimethyl-3-oxo-2-oxabicyclo[3.2.1]octan-7-yl]-2,16-dimethyl-8-oxapentacyclo[9.7.0.02,7.07,9.012,16]octadecan-3-one
SMILES (Canonical) CC12CCC3C(C1CCC2(C4CC5(CC4OC(=O)C5(C)O)C)O)CC6C7(C3(C(=O)CCC7)C)O6
SMILES (Isomeric) C[C@]12CC[C@H]3[C@H]([C@@H]1CC[C@]2([C@H]4C[C@@]5(C[C@H]4OC(=O)[C@]5(C)O)C)O)C[C@@H]6[C@]7([C@@]3(C(=O)CCC7)C)O6
InChI InChI=1S/C28H40O6/c1-23-13-18(19(14-23)33-22(30)26(23,4)31)27(32)11-8-16-15-12-21-28(34-21)9-5-6-20(29)25(28,3)17(15)7-10-24(16,27)2/h15-19,21,31-32H,5-14H2,1-4H3/t15-,16-,17-,18-,19+,21+,23+,24-,25-,26-,27+,28+/m0/s1
InChI Key PFSSPHXISVKZBM-RNDHMNKTSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C28H40O6
Molecular Weight 472.60 g/mol
Exact Mass 472.28248899 g/mol
Topological Polar Surface Area (TPSA) 96.40 Ų
XlogP 3.00
Atomic LogP (AlogP) 3.55
H-Bond Acceptor 6
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Acnistin G

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9219 92.19%
Caco-2 - 0.6608 66.08%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability + 0.6143 61.43%
Subcellular localzation Mitochondria 0.7240 72.40%
OATP2B1 inhibitior - 0.5734 57.34%
OATP1B1 inhibitior + 0.8837 88.37%
OATP1B3 inhibitior + 0.7995 79.95%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.8108 81.08%
BSEP inhibitior + 0.8531 85.31%
P-glycoprotein inhibitior - 0.5345 53.45%
P-glycoprotein substrate - 0.6174 61.74%
CYP3A4 substrate + 0.7078 70.78%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8515 85.15%
CYP3A4 inhibition - 0.6970 69.70%
CYP2C9 inhibition - 0.8718 87.18%
CYP2C19 inhibition - 0.8785 87.85%
CYP2D6 inhibition - 0.9623 96.23%
CYP1A2 inhibition - 0.7577 75.77%
CYP2C8 inhibition + 0.5519 55.19%
CYP inhibitory promiscuity - 0.9882 98.82%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Non-required 0.6186 61.86%
Eye corrosion - 0.9907 99.07%
Eye irritation - 0.9497 94.97%
Skin irritation - 0.5573 55.73%
Skin corrosion - 0.8847 88.47%
Ames mutagenesis - 0.6200 62.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5490 54.90%
Micronuclear - 0.7100 71.00%
Hepatotoxicity + 0.5250 52.50%
skin sensitisation - 0.8845 88.45%
Respiratory toxicity + 0.8222 82.22%
Reproductive toxicity + 0.8667 86.67%
Mitochondrial toxicity + 0.9000 90.00%
Nephrotoxicity + 0.5351 53.51%
Acute Oral Toxicity (c) I 0.4682 46.82%
Estrogen receptor binding + 0.8012 80.12%
Androgen receptor binding + 0.7579 75.79%
Thyroid receptor binding + 0.5397 53.97%
Glucocorticoid receptor binding + 0.7759 77.59%
Aromatase binding + 0.7391 73.91%
PPAR gamma + 0.5770 57.70%
Honey bee toxicity - 0.7696 76.96%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity + 0.6100 61.00%
Fish aquatic toxicity + 0.9464 94.64%

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 92.82% 97.25%
CHEMBL3137262 O60341 LSD1/CoREST complex 91.94% 97.09%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.65% 96.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 90.37% 94.45%
CHEMBL1994 P08235 Mineralocorticoid receptor 89.96% 100.00%
CHEMBL241 Q14432 Phosphodiesterase 3A 89.86% 92.94%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 89.62% 99.23%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 87.22% 85.14%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 86.67% 93.04%
CHEMBL1937 Q92769 Histone deacetylase 2 85.48% 94.75%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 84.77% 94.00%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 84.51% 82.69%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 84.41% 91.11%
CHEMBL259 P32245 Melanocortin receptor 4 83.50% 95.38%
CHEMBL1914 P06276 Butyrylcholinesterase 83.48% 95.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 82.94% 95.56%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 82.65% 92.62%
CHEMBL1293249 Q13887 Kruppel-like factor 5 82.63% 86.33%
CHEMBL4685 P14902 Indoleamine 2,3-dioxygenase 80.92% 96.38%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 80.63% 97.14%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 80.53% 95.50%
CHEMBL5255 O00206 Toll-like receptor 4 80.50% 92.50%
CHEMBL332 P03956 Matrix metalloproteinase-1 80.05% 94.50%

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.
Saracha nigribaccata

Cross-Links

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PubChem 101666190
LOTUS LTS0256247
wikiData Q105207960