from Rollinia papilionella

Details

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Internal ID 6881e999-564f-4988-a0d0-3e2d745e672e
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohols > Annonaceous acetogenins
IUPAC Name 3-[13-hydroxy-13-[5-[5-(1-hydroxyundecyl)oxolan-2-yl]oxolan-2-yl]-12-oxotridecyl]-5-methyloxolan-2-one
SMILES (Canonical) CCCCCCCCCCC(C1CCC(O1)C2CCC(O2)C(C(=O)CCCCCCCCCCCC3CC(OC3=O)C)O)O
SMILES (Isomeric) CCCCCCCCCCC(C1CCC(O1)C2CCC(O2)C(C(=O)CCCCCCCCCCCC3CC(OC3=O)C)O)O
InChI InChI=1S/C37H66O7/c1-3-4-5-6-7-12-15-18-21-30(38)32-23-24-33(43-32)34-25-26-35(44-34)36(40)31(39)22-19-16-13-10-8-9-11-14-17-20-29-27-28(2)42-37(29)41/h28-30,32-36,38,40H,3-27H2,1-2H3
InChI Key XXWGMJIUQNJXMV-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C37H66O7
Molecular Weight 622.90 g/mol
Exact Mass 622.48085444 g/mol
Topological Polar Surface Area (TPSA) 102.00 Ų
XlogP 10.10
Atomic LogP (AlogP) 8.15
H-Bond Acceptor 7
H-Bond Donor 2
Rotatable Bonds 25

Synonyms

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CHEMBL506028
NSC364581
NSC-364581
B806512K271
2(3H)-Furanone,2'-bifuran]-5-yl]- 12-oxotridecyl]-5-methyl-

2D Structure

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2D Structure of from Rollinia papilionella

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9146 91.46%
Caco-2 - 0.8040 80.40%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability - 0.7571 75.71%
Subcellular localzation Mitochondria 0.8043 80.43%
OATP2B1 inhibitior - 0.5625 56.25%
OATP1B1 inhibitior + 0.8765 87.65%
OATP1B3 inhibitior + 0.8750 87.50%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior + 0.8059 80.59%
P-glycoprotein inhibitior + 0.6377 63.77%
P-glycoprotein substrate + 0.5732 57.32%
CYP3A4 substrate + 0.6245 62.45%
CYP2C9 substrate - 0.7891 78.91%
CYP2D6 substrate - 0.8505 85.05%
CYP3A4 inhibition - 0.7142 71.42%
CYP2C9 inhibition - 0.8802 88.02%
CYP2C19 inhibition - 0.8221 82.21%
CYP2D6 inhibition - 0.9420 94.20%
CYP1A2 inhibition - 0.8503 85.03%
CYP2C8 inhibition - 0.6658 66.58%
CYP inhibitory promiscuity - 0.9674 96.74%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.6799 67.99%
Eye corrosion - 0.9859 98.59%
Eye irritation - 0.8484 84.84%
Skin irritation - 0.6206 62.06%
Skin corrosion - 0.8981 89.81%
Ames mutagenesis - 0.7000 70.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4674 46.74%
Micronuclear - 0.9000 90.00%
Hepatotoxicity + 0.5192 51.92%
skin sensitisation - 0.9242 92.42%
Respiratory toxicity + 0.5667 56.67%
Reproductive toxicity + 0.5535 55.35%
Mitochondrial toxicity + 0.7875 78.75%
Nephrotoxicity + 0.6869 68.69%
Acute Oral Toxicity (c) III 0.4168 41.68%
Estrogen receptor binding + 0.7946 79.46%
Androgen receptor binding + 0.6418 64.18%
Thyroid receptor binding - 0.6340 63.40%
Glucocorticoid receptor binding - 0.5768 57.68%
Aromatase binding - 0.4904 49.04%
PPAR gamma - 0.5304 53.04%
Honey bee toxicity - 0.8999 89.99%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity + 0.6842 68.42%
Fish aquatic toxicity + 0.9478 94.78%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.69% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 97.23% 97.25%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 95.90% 85.94%
CHEMBL3060 Q9Y345 Glycine transporter 2 95.83% 99.17%
CHEMBL2581 P07339 Cathepsin D 95.25% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.06% 91.11%
CHEMBL3137262 O60341 LSD1/CoREST complex 89.89% 97.09%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 89.69% 100.00%
CHEMBL5255 O00206 Toll-like receptor 4 86.69% 92.50%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 86.27% 90.71%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 85.84% 99.23%
CHEMBL4227 P25090 Lipoxin A4 receptor 85.69% 100.00%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 85.06% 96.47%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 84.99% 97.29%
CHEMBL299 P17252 Protein kinase C alpha 84.53% 98.03%
CHEMBL230 P35354 Cyclooxygenase-2 84.38% 89.63%
CHEMBL6136 O60341 Lysine-specific histone demethylase 1 83.93% 95.58%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 83.23% 91.81%
CHEMBL340 P08684 Cytochrome P450 3A4 83.16% 91.19%
CHEMBL3401 O75469 Pregnane X receptor 82.30% 94.73%
CHEMBL4588 P22894 Matrix metalloproteinase 8 82.19% 94.66%
CHEMBL3359 P21462 Formyl peptide receptor 1 82.00% 93.56%
CHEMBL1795139 Q8IU80 Transmembrane protease serine 6 81.51% 98.33%
CHEMBL1806 P11388 DNA topoisomerase II alpha 81.04% 89.00%
CHEMBL1075162 Q13304 Uracil nucleotide/cysteinyl leukotriene receptor 81.00% 80.33%
CHEMBL4685 P14902 Indoleamine 2,3-dioxygenase 80.66% 96.38%
CHEMBL2001 Q9H244 Purinergic receptor P2Y12 80.46% 96.00%

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.
Annona papilionella
Annona rensoniana

Cross-Links

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PubChem 339203
LOTUS LTS0246073
wikiData Q105344250