Desacetyluvaricin

Details

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Internal ID a7a61f16-52f6-4a47-a5b6-53cdbcba4224
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohols > Annonaceous acetogenins
IUPAC Name (2S)-4-[(13R)-13-hydroxy-13-[(2R,5R)-5-[(2R,5R)-5-[(1S)-1-hydroxyundecyl]oxolan-2-yl]oxolan-2-yl]tridecyl]-2-methyl-2H-furan-5-one
SMILES (Canonical) CCCCCCCCCCC(C1CCC(O1)C2CCC(O2)C(CCCCCCCCCCCCC3=CC(OC3=O)C)O)O
SMILES (Isomeric) CCCCCCCCCC[C@@H]([C@H]1CC[C@@H](O1)[C@H]2CC[C@@H](O2)[C@@H](CCCCCCCCCCCCC3=C[C@@H](OC3=O)C)O)O
InChI InChI=1S/C37H66O6/c1-3-4-5-6-7-13-16-19-22-31(38)33-24-26-35(42-33)36-27-25-34(43-36)32(39)23-20-17-14-11-9-8-10-12-15-18-21-30-28-29(2)41-37(30)40/h28-29,31-36,38-39H,3-27H2,1-2H3/t29-,31-,32+,33+,34+,35+,36+/m0/s1
InChI Key URLVCROWVOSNPT-HJPPHTJLSA-N
Popularity 9 references in papers

Physical and Chemical Properties

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Molecular Formula C37H66O6
Molecular Weight 606.90 g/mol
Exact Mass 606.48593982 g/mol
Topological Polar Surface Area (TPSA) 85.20 Ų
XlogP 11.20
Atomic LogP (AlogP) 8.89
H-Bond Acceptor 6
H-Bond Donor 2
Rotatable Bonds 25

Synonyms

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BULLANIN
CHEMBL145449
98767-45-4
SCHEMBL11961385
DTXSID10913091
C37H66O6
BDBM50094725
(2S)-4-[(13R)-13-hydroxy-13-[(2R,5R)-5-[(2R,5R)-5-[(1S)-1-hydroxyundecyl]oxolan-2-yl]oxolan-2-yl]tridecyl]-2-methyl-2H-furan-5-one
2(5H)-Puranone, 3-(13-hydroxy-13-(octahydro-5'-(1-hydroxyundecyl)(2,2'-bifuran)-5-yl)tridecyl)-5-methyl-
3-{13-Hydroxy-13-[5''-(1-hydroxy-undecyl)-octahydro-[2,2'']bifuranyl-5-yl]-tridecyl}-5-methyl-5H-furan-2-one(Desacetyluvaricin)
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Desacetyluvaricin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9762 97.62%
Caco-2 - 0.8014 80.14%
Blood Brain Barrier + 0.5105 51.05%
Human oral bioavailability - 0.7857 78.57%
Subcellular localzation Mitochondria 0.7725 77.25%
OATP2B1 inhibitior - 0.5644 56.44%
OATP1B1 inhibitior + 0.8760 87.60%
OATP1B3 inhibitior + 0.9352 93.52%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior + 0.6285 62.85%
P-glycoprotein inhibitior + 0.6328 63.28%
P-glycoprotein substrate - 0.6155 61.55%
CYP3A4 substrate + 0.6184 61.84%
CYP2C9 substrate - 0.6043 60.43%
CYP2D6 substrate - 0.8694 86.94%
CYP3A4 inhibition - 0.7070 70.70%
CYP2C9 inhibition - 0.8653 86.53%
CYP2C19 inhibition - 0.6620 66.20%
CYP2D6 inhibition - 0.9054 90.54%
CYP1A2 inhibition - 0.7836 78.36%
CYP2C8 inhibition - 0.7071 70.71%
CYP inhibitory promiscuity - 0.8039 80.39%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.5983 59.83%
Eye corrosion - 0.9874 98.74%
Eye irritation - 0.8563 85.63%
Skin irritation - 0.5841 58.41%
Skin corrosion - 0.9323 93.23%
Ames mutagenesis - 0.7037 70.37%
Human Ether-a-go-go-Related Gene inhibition - 0.4285 42.85%
Micronuclear - 0.9000 90.00%
Hepatotoxicity - 0.5541 55.41%
skin sensitisation - 0.8256 82.56%
Respiratory toxicity + 0.6333 63.33%
Reproductive toxicity + 0.6778 67.78%
Mitochondrial toxicity + 0.7375 73.75%
Nephrotoxicity + 0.7993 79.93%
Acute Oral Toxicity (c) III 0.4228 42.28%
Estrogen receptor binding + 0.7599 75.99%
Androgen receptor binding + 0.5330 53.30%
Thyroid receptor binding - 0.6401 64.01%
Glucocorticoid receptor binding - 0.5891 58.91%
Aromatase binding + 0.5899 58.99%
PPAR gamma - 0.5096 50.96%
Honey bee toxicity - 0.9363 93.63%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity + 0.6500 65.00%
Fish aquatic toxicity + 0.9781 97.81%

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 96.27% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.78% 96.09%
CHEMBL2581 P07339 Cathepsin D 94.81% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.45% 91.11%
CHEMBL3401 O75469 Pregnane X receptor 91.68% 94.73%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 90.30% 85.94%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 88.64% 100.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 88.34% 99.17%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.36% 95.56%
CHEMBL3137262 O60341 LSD1/CoREST complex 85.55% 97.09%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 85.54% 90.71%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.04% 86.33%
CHEMBL1907 P15144 Aminopeptidase N 82.66% 93.31%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.71% 99.23%
CHEMBL3359 P21462 Formyl peptide receptor 1 81.04% 93.56%

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.
Annona mucosa
Annona muricata
Annona spinescens
Annona squamosa
Asimina triloba
Uvaria chamae

Cross-Links

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PubChem 127149
NPASS NPC292809
ChEMBL CHEMBL145449
LOTUS LTS0039727
wikiData Q82883616