cis-Sylvaticin

Details

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Internal ID 21c769db-a7d5-4984-bb3a-fbabf5993130
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohols > Annonaceous acetogenins
IUPAC Name (2S)-4-[(2R)-9-[(2S,5S)-5-[(1S,4S)-1,4-dihydroxy-4-[(2S,5R)-5-[(1S)-1-hydroxyundecyl]oxolan-2-yl]butyl]oxolan-2-yl]-2-hydroxynonyl]-2-methyl-2H-furan-5-one
SMILES (Canonical) CCCCCCCCCCC(C1CCC(O1)C(CCC(C2CCC(O2)CCCCCCCC(CC3=CC(OC3=O)C)O)O)O)O
SMILES (Isomeric) CCCCCCCCCC[C@@H]([C@H]1CC[C@H](O1)[C@H](CC[C@@H]([C@@H]2CC[C@@H](O2)CCCCCCC[C@H](CC3=C[C@@H](OC3=O)C)O)O)O)O
InChI InChI=1S/C37H66O8/c1-3-4-5-6-7-8-12-15-18-31(39)35-23-24-36(45-35)33(41)21-20-32(40)34-22-19-30(44-34)17-14-11-9-10-13-16-29(38)26-28-25-27(2)43-37(28)42/h25,27,29-36,38-41H,3-24,26H2,1-2H3/t27-,29+,30-,31-,32-,33-,34-,35+,36-/m0/s1
InChI Key HKMBLJVHVBJAIH-PDXBLBMYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C37H66O8
Molecular Weight 638.90 g/mol
Exact Mass 638.47576906 g/mol
Topological Polar Surface Area (TPSA) 126.00 Ų
XlogP 8.20
Atomic LogP (AlogP) 6.83
H-Bond Acceptor 8
H-Bond Donor 4
Rotatable Bonds 25

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of cis-Sylvaticin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9685 96.85%
Caco-2 - 0.8388 83.88%
Blood Brain Barrier + 0.5355 53.55%
Human oral bioavailability - 0.7143 71.43%
Subcellular localzation Mitochondria 0.7433 74.33%
OATP2B1 inhibitior - 0.5659 56.59%
OATP1B1 inhibitior + 0.8738 87.38%
OATP1B3 inhibitior + 0.9400 94.00%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.7070 70.70%
BSEP inhibitior + 0.6460 64.60%
P-glycoprotein inhibitior + 0.6226 62.26%
P-glycoprotein substrate - 0.5411 54.11%
CYP3A4 substrate + 0.6325 63.25%
CYP2C9 substrate - 0.6043 60.43%
CYP2D6 substrate - 0.8694 86.94%
CYP3A4 inhibition - 0.6168 61.68%
CYP2C9 inhibition - 0.8834 88.34%
CYP2C19 inhibition - 0.6454 64.54%
CYP2D6 inhibition - 0.8954 89.54%
CYP1A2 inhibition - 0.7870 78.70%
CYP2C8 inhibition - 0.6981 69.81%
CYP inhibitory promiscuity - 0.8548 85.48%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.6002 60.02%
Eye corrosion - 0.9875 98.75%
Eye irritation - 0.8751 87.51%
Skin irritation - 0.5384 53.84%
Skin corrosion - 0.9287 92.87%
Ames mutagenesis - 0.7620 76.20%
Human Ether-a-go-go-Related Gene inhibition - 0.4213 42.13%
Micronuclear - 0.9100 91.00%
Hepatotoxicity - 0.5895 58.95%
skin sensitisation - 0.8111 81.11%
Respiratory toxicity + 0.6778 67.78%
Reproductive toxicity + 0.6778 67.78%
Mitochondrial toxicity + 0.7500 75.00%
Nephrotoxicity + 0.7992 79.92%
Acute Oral Toxicity (c) III 0.4485 44.85%
Estrogen receptor binding + 0.7333 73.33%
Androgen receptor binding + 0.5463 54.63%
Thyroid receptor binding - 0.6440 64.40%
Glucocorticoid receptor binding - 0.6049 60.49%
Aromatase binding + 0.5581 55.81%
PPAR gamma - 0.5446 54.46%
Honey bee toxicity - 0.9269 92.69%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity + 0.6303 63.03%
Fish aquatic toxicity + 0.9718 97.18%

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 98.23% 98.95%
CHEMBL253 P34972 Cannabinoid CB2 receptor 94.29% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.98% 96.09%
CHEMBL3401 O75469 Pregnane X receptor 91.01% 94.73%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.99% 91.11%
CHEMBL3060 Q9Y345 Glycine transporter 2 90.87% 99.17%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.46% 95.56%
CHEMBL230 P35354 Cyclooxygenase-2 89.54% 89.63%
CHEMBL3137262 O60341 LSD1/CoREST complex 88.11% 97.09%
CHEMBL3359 P21462 Formyl peptide receptor 1 87.09% 93.56%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 86.66% 92.08%
CHEMBL1907605 P24864 Cyclin-dependent kinase 2/cyclin E1 86.65% 92.88%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 86.18% 97.29%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.07% 86.33%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 86.06% 100.00%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 83.67% 90.71%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 83.57% 92.86%
CHEMBL2996 Q05655 Protein kinase C delta 83.18% 97.79%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 82.28% 91.81%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.99% 99.23%
CHEMBL1907 P15144 Aminopeptidase N 80.01% 93.31%

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 squamosa

Cross-Links

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PubChem 11990359
NPASS NPC93063
LOTUS LTS0227880
wikiData Q105029752