Goniodenin

Details

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Internal ID 4c49fc43-e00b-4d01-b65f-768353c9d2f3
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohols > Annonaceous acetogenins
IUPAC Name (2S)-4-[(2R)-2-hydroxy-7-[(2R,5S)-5-[(2S,5S)-5-[(E,1S)-1-hydroxyheptadec-4-enyl]oxolan-2-yl]oxolan-2-yl]heptyl]-2-methyl-2H-furan-5-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C37H64O6/c1-3-4-5-6-7-8-9-10-11-12-13-14-15-19-22-33(39)34-25-26-36(43-34)35-24-23-32(42-35)21-18-16-17-20-31(38)28-30-27-29(2)41-37(30)40/h14-15,27,29,31-36,38-39H,3-13,16-26,28H2,1-2H3/b15-14+/t29-,31+,32+,33-,34-,35-,36-/m0/s1
InChI Key RMBBAMZXSGKPBA-DNKCGJNDSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C37H64O6
Molecular Weight 604.90 g/mol
Exact Mass 604.47028976 g/mol
Topological Polar Surface Area (TPSA) 85.20 Ų
XlogP 10.10
Atomic LogP (AlogP) 8.66
H-Bond Acceptor 6
H-Bond Donor 2
Rotatable Bonds 24

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Goniodenin

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 - 0.8280 82.80%
Blood Brain Barrier + 0.5105 51.05%
Human oral bioavailability - 0.7429 74.29%
Subcellular localzation Mitochondria 0.7725 77.25%
OATP2B1 inhibitior - 0.5685 56.85%
OATP1B1 inhibitior + 0.8134 81.34%
OATP1B3 inhibitior + 0.9352 93.52%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior + 0.8007 80.07%
P-glycoprotein inhibitior + 0.6420 64.20%
P-glycoprotein substrate + 0.5218 52.18%
CYP3A4 substrate + 0.6627 66.27%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8673 86.73%
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 + 0.5149 51.49%
CYP inhibitory promiscuity - 0.8039 80.39%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.5983 59.83%
Eye corrosion - 0.9874 98.74%
Eye irritation - 0.9014 90.14%
Skin irritation - 0.5841 58.41%
Skin corrosion - 0.9323 93.23%
Ames mutagenesis - 0.7520 75.20%
Human Ether-a-go-go-Related Gene inhibition - 0.3911 39.11%
Micronuclear - 0.9000 90.00%
Hepatotoxicity - 0.5573 55.73%
skin sensitisation - 0.8256 82.56%
Respiratory toxicity + 0.7111 71.11%
Reproductive toxicity + 0.6778 67.78%
Mitochondrial toxicity + 0.7375 73.75%
Nephrotoxicity + 0.7734 77.34%
Acute Oral Toxicity (c) III 0.4228 42.28%
Estrogen receptor binding + 0.7555 75.55%
Androgen receptor binding + 0.5850 58.50%
Thyroid receptor binding - 0.6589 65.89%
Glucocorticoid receptor binding - 0.6233 62.33%
Aromatase binding - 0.4929 49.29%
PPAR gamma - 0.5066 50.66%
Honey bee toxicity - 0.8804 88.04%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity + 0.6475 64.75%
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
CHEMBL2581 P07339 Cathepsin D 96.53% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 94.95% 99.17%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.98% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.80% 96.09%
CHEMBL230 P35354 Cyclooxygenase-2 92.29% 89.63%
CHEMBL3401 O75469 Pregnane X receptor 92.12% 94.73%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.12% 95.56%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 89.23% 100.00%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 87.72% 97.29%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 87.06% 85.94%
CHEMBL253 P34972 Cannabinoid CB2 receptor 86.58% 97.25%
CHEMBL3359 P21462 Formyl peptide receptor 1 84.72% 93.56%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 84.11% 96.47%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 84.08% 92.08%
CHEMBL3137262 O60341 LSD1/CoREST complex 83.37% 97.09%
CHEMBL4581 P52732 Kinesin-like protein 1 83.27% 93.18%
CHEMBL1907605 P24864 Cyclin-dependent kinase 2/cyclin E1 83.07% 92.88%
CHEMBL4227 P25090 Lipoxin A4 receptor 81.74% 100.00%
CHEMBL2781 P19634 Sodium/hydrogen exchanger 1 81.56% 90.24%
CHEMBL6136 O60341 Lysine-specific histone demethylase 1 81.14% 95.58%
CHEMBL2069156 Q14145 Kelch-like ECH-associated protein 1 80.65% 82.38%
CHEMBL4588 P22894 Matrix metalloproteinase 8 80.31% 94.66%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 80.23% 91.81%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.08% 99.23%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.00% 95.89%

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.
Goniothalamus giganteus

Cross-Links

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PubChem 101926326
LOTUS LTS0150459
wikiData Q105240674