L-erythro-L-glycero-D-altro-7-Trideculo-7,4-furanosonic acid, 2,7-anhydro-3,4-di-C-carboxy-8,9,10,12,13-pentadeoxy-12-(phenylmethyl)-, 11-acetate 5-((4E,6R)-6-methyl-9-phenyl-4-nonenoate), (7S)-

Details

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Internal ID 20c1556f-588a-49e1-82c0-d392b3f1ed8e
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Pentacarboxylic acids and derivatives
IUPAC Name (1S,3S,4S,5R,6R,7R)-1-[(4R,5R)-4-acetyloxy-5-methyl-6-phenylhexyl]-4,7-dihydroxy-6-[(E,6R)-6-methyl-9-phenylnon-4-enoyl]oxy-2,8-dioxabicyclo[3.2.1]octane-3,4,5-tricarboxylic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C40H50O14/c1-25(15-12-20-28-16-6-4-7-17-28)14-10-11-22-31(42)52-33-32(43)38(53-34(35(44)45)39(50,36(46)47)40(33,54-38)37(48)49)23-13-21-30(51-27(3)41)26(2)24-29-18-8-5-9-19-29/h4-10,14,16-19,25-26,30,32-34,43,50H,11-13,15,20-24H2,1-3H3,(H,44,45)(H,46,47)(H,48,49)/b14-10+/t25-,26+,30+,32+,33+,34+,38-,39+,40-/m0/s1
InChI Key KQMNJFMTGHRJHM-ZFSXNWTMSA-N
Popularity 20 references in papers

Physical and Chemical Properties

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Molecular Formula C40H50O14
Molecular Weight 754.80 g/mol
Exact Mass 754.32005626 g/mol
Topological Polar Surface Area (TPSA) 223.00 Ų
XlogP 5.50
Atomic LogP (AlogP) 4.08
H-Bond Acceptor 11
H-Bond Donor 5
Rotatable Bonds 20

Synonyms

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(+)-Zaragozic acid
146389-62-0
Zaragozic acid C [MI]
UNII-04ISX24T1B
04ISX24T1B
L-697350
CHEMBL505374
CHEBI:83934
L-Erythro-L-glycero-D-altro-7-trideculo-7,4-furanosonic acid, 2,7-anhydro-3,4-di-c-carboxy-8,9,10,12,13-pentadeoxy-12-(phenylmethyl)-, 11-acetate 5-((4E,6R)-6-methyl-9-phenyl-4-nonenoate), (7S)-
(1S,3S,4S,5R,6R,7R)-1-((4R,5R)-4-acetoxy-5-methyl-6-phenylhexyl)-4,7-dihydroxy-6-(((R,E)-6-methyl-9-phenylnon-4-enoyl)oxy)-2,8-dioxabicyclo[3.2.1]octane-3,4,5-tricarboxylic acid
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of L-erythro-L-glycero-D-altro-7-Trideculo-7,4-furanosonic acid, 2,7-anhydro-3,4-di-C-carboxy-8,9,10,12,13-pentadeoxy-12-(phenylmethyl)-, 11-acetate 5-((4E,6R)-6-methyl-9-phenyl-4-nonenoate), (7S)-

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.6196 61.96%
Caco-2 - 0.8665 86.65%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability - 0.7429 74.29%
Subcellular localzation Mitochondria 0.7552 75.52%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8110 81.10%
OATP1B3 inhibitior - 0.3148 31.48%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.6500 65.00%
BSEP inhibitior + 0.8788 87.88%
P-glycoprotein inhibitior + 0.7559 75.59%
P-glycoprotein substrate + 0.7358 73.58%
CYP3A4 substrate + 0.6980 69.80%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8777 87.77%
CYP3A4 inhibition - 0.7996 79.96%
CYP2C9 inhibition - 0.8295 82.95%
CYP2C19 inhibition - 0.8105 81.05%
CYP2D6 inhibition - 0.9410 94.10%
CYP1A2 inhibition - 0.8503 85.03%
CYP2C8 inhibition + 0.7404 74.04%
CYP inhibitory promiscuity - 0.9305 93.05%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Non-required 0.6193 61.93%
Eye corrosion - 0.9917 99.17%
Eye irritation - 0.9128 91.28%
Skin irritation - 0.6433 64.33%
Skin corrosion - 0.9202 92.02%
Ames mutagenesis - 0.5100 51.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6901 69.01%
Micronuclear - 0.7200 72.00%
Hepatotoxicity - 0.5734 57.34%
skin sensitisation - 0.8948 89.48%
Respiratory toxicity + 0.6889 68.89%
Reproductive toxicity + 0.7222 72.22%
Mitochondrial toxicity + 0.8250 82.50%
Nephrotoxicity - 0.6610 66.10%
Acute Oral Toxicity (c) I 0.5085 50.85%
Estrogen receptor binding + 0.8365 83.65%
Androgen receptor binding + 0.7354 73.54%
Thyroid receptor binding + 0.5805 58.05%
Glucocorticoid receptor binding + 0.7290 72.90%
Aromatase binding + 0.5669 56.69%
PPAR gamma + 0.7052 70.52%
Honey bee toxicity - 0.7146 71.46%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity + 0.5445 54.45%
Fish aquatic toxicity + 0.9964 99.64%

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
CHEMBL2581 P07339 Cathepsin D 98.34% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.69% 96.09%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 97.13% 94.62%
CHEMBL221 P23219 Cyclooxygenase-1 96.21% 90.17%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.68% 91.11%
CHEMBL3060 Q9Y345 Glycine transporter 2 93.95% 99.17%
CHEMBL1821 P08173 Muscarinic acetylcholine receptor M4 93.32% 94.08%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.72% 86.33%
CHEMBL3401 O75469 Pregnane X receptor 89.08% 94.73%
CHEMBL5939 Q9NZ08 Endoplasmic reticulum aminopeptidase 1 89.07% 100.00%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 87.48% 95.50%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 85.24% 95.89%
CHEMBL3359 P21462 Formyl peptide receptor 1 84.77% 93.56%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.01% 95.56%
CHEMBL340 P08684 Cytochrome P450 3A4 83.48% 91.19%
CHEMBL5028 O14672 ADAM10 82.10% 97.50%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 81.51% 93.00%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 81.06% 96.00%
CHEMBL4227 P25090 Lipoxin A4 receptor 80.78% 100.00%

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.
There are no matching plants.

Cross-Links

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PubChem 11814656
LOTUS LTS0082505
wikiData Q27089281