CID 461349

Details

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Internal ID e6e2be4f-4cf2-4ac5-a300-db8748a2a399
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Amino acids, peptides, and analogues > Peptides > Oligopeptides
IUPAC Name [5-[2-[3-(3-amino-1-hydroxy-3-oxopropyl)-18-(hexadecanoylamino)-11,21,25-trihydroxy-15-(1-hydroxyethyl)-26-methyl-2,5,8,14,17,23-hexaoxo-1,4,7,13,16,22-hexazatricyclo[22.3.0.09,13]heptacosan-6-yl]-2-hydroxyethyl]-2-hydroxyphenyl] hydrogen sulfate
SMILES (Canonical) CCCCCCCCCCCCCCCC(=O)NC1CCC(NC(=O)C2C(C(CN2C(=O)C(NC(=O)C(NC(=O)C3CC(CN3C(=O)C(NC1=O)C(C)O)O)C(CC4=CC(=C(C=C4)O)OS(=O)(=O)O)O)C(CC(=O)N)O)C)O)O
SMILES (Isomeric) CCCCCCCCCCCCCCCC(=O)NC1CCC(NC(=O)C2C(C(CN2C(=O)C(NC(=O)C(NC(=O)C3CC(CN3C(=O)C(NC1=O)C(C)O)O)C(CC4=CC(=C(C=C4)O)OS(=O)(=O)O)O)C(CC(=O)N)O)C)O)O
InChI InChI=1S/C51H82N8O19S/c1-4-5-6-7-8-9-10-11-12-13-14-15-16-17-39(66)53-32-19-21-40(67)54-49(72)44-45(68)28(2)26-59(44)51(74)43(36(64)25-38(52)65)57-48(71)42(35(63)22-30-18-20-34(62)37(23-30)78-79(75,76)77)56-47(70)33-24-31(61)27-58(33)50(73)41(29(3)60)55-46(32)69/h18,20,23,28-29,31-33,35-36,40-45,60-64,67-68H,4-17,19,21-22,24-27H2,1-3H3,(H2,52,65)(H,53,66)(H,54,72)(H,55,69)(H,56,70)(H,57,71)(H,75,76,77)
InChI Key BQHILXLXXUQKOO-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C51H82N8O19S
Molecular Weight 1143.30 g/mol
Exact Mass 1142.54169359 g/mol
Topological Polar Surface Area (TPSA) 443.00 Ų
XlogP 2.60
Atomic LogP (AlogP) -2.09
H-Bond Acceptor 18
H-Bond Donor 14
Rotatable Bonds 24

Synonyms

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[5-[2-[(3-amino-1-hydroxy-3-oxo-propyl)-(hexadecanoylamino)-trihydroxy-(1-hydroxyethyl)-methyl-hexaoxo-[?]yl]-2-hydroxy-ethyl]-2-hydroxy-phenyl] hydrogen sulfate
[5-[2-[3-(3-Amino-1-hydroxy-3-oxopropyl)-18-(hexadecanoylamino)-11,21,25-trihydroxy-15-(1-hydroxyethyl)-26-methyl-2,5,8,14,17,23-hexaoxo-1,4,7,13,16,22-hexazatricyclo[22.3.0.09,13]heptacosan-6-yl]-2-hydroxyethyl]-2-hydroxyphenyl] hydrogen sulfate

2D Structure

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2D Structure of CID 461349

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.6850 68.50%
Caco-2 - 0.8600 86.00%
Blood Brain Barrier - 0.6750 67.50%
Human oral bioavailability - 0.7000 70.00%
Subcellular localzation Mitochondria 0.3923 39.23%
OATP2B1 inhibitior - 0.8607 86.07%
OATP1B1 inhibitior + 0.8372 83.72%
OATP1B3 inhibitior + 0.9241 92.41%
MATE1 inhibitior - 0.8000 80.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior + 0.8239 82.39%
P-glycoprotein inhibitior + 0.7407 74.07%
P-glycoprotein substrate + 0.8621 86.21%
CYP3A4 substrate + 0.7361 73.61%
CYP2C9 substrate - 0.8065 80.65%
CYP2D6 substrate - 0.8154 81.54%
CYP3A4 inhibition - 0.8607 86.07%
CYP2C9 inhibition - 0.7895 78.95%
CYP2C19 inhibition - 0.7621 76.21%
CYP2D6 inhibition - 0.8522 85.22%
CYP1A2 inhibition - 0.7983 79.83%
CYP2C8 inhibition + 0.8279 82.79%
CYP inhibitory promiscuity - 0.9576 95.76%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) + 0.5300 53.00%
Carcinogenicity (trinary) Non-required 0.6174 61.74%
Eye corrosion - 0.9788 97.88%
Eye irritation - 0.8978 89.78%
Skin irritation - 0.7616 76.16%
Skin corrosion - 0.9102 91.02%
Ames mutagenesis - 0.7000 70.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3730 37.30%
Micronuclear + 0.8900 89.00%
Hepatotoxicity + 0.6106 61.06%
skin sensitisation - 0.8401 84.01%
Respiratory toxicity + 0.7778 77.78%
Reproductive toxicity + 0.9222 92.22%
Mitochondrial toxicity + 0.7250 72.50%
Nephrotoxicity - 0.6525 65.25%
Acute Oral Toxicity (c) III 0.5811 58.11%
Estrogen receptor binding + 0.7710 77.10%
Androgen receptor binding + 0.7347 73.47%
Thyroid receptor binding + 0.5677 56.77%
Glucocorticoid receptor binding + 0.5904 59.04%
Aromatase binding + 0.6454 64.54%
PPAR gamma + 0.7659 76.59%
Honey bee toxicity - 0.7265 72.65%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity + 0.6465 64.65%
Fish aquatic toxicity + 0.9550 95.50%

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 99.85% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 99.61% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 97.85% 99.17%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 97.60% 94.45%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.17% 91.11%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 96.92% 90.71%
CHEMBL3137262 O60341 LSD1/CoREST complex 96.22% 97.09%
CHEMBL5469 Q14289 Protein tyrosine kinase 2 beta 93.75% 91.03%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 93.53% 92.08%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.39% 95.56%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 92.83% 100.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 92.17% 95.89%
CHEMBL4581 P52732 Kinesin-like protein 1 91.18% 93.18%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 90.85% 82.69%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 90.29% 92.86%
CHEMBL3392948 Q9NP59 Solute carrier family 40 member 1 88.68% 95.00%
CHEMBL340 P08684 Cytochrome P450 3A4 88.16% 91.19%
CHEMBL2001 Q9H244 Purinergic receptor P2Y12 88.05% 96.00%
CHEMBL1907605 P24864 Cyclin-dependent kinase 2/cyclin E1 88.01% 92.88%
CHEMBL3359 P21462 Formyl peptide receptor 1 87.96% 93.56%
CHEMBL5163 Q9NY46 Sodium channel protein type III alpha subunit 87.76% 96.90%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 87.31% 97.14%
CHEMBL2535 P11166 Glucose transporter 86.14% 98.75%
CHEMBL4588 P22894 Matrix metalloproteinase 8 85.87% 94.66%
CHEMBL218 P21554 Cannabinoid CB1 receptor 85.38% 96.61%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 85.36% 94.33%
CHEMBL255 P29275 Adenosine A2b receptor 84.94% 98.59%
CHEMBL1907594 P30926 Neuronal acetylcholine receptor; alpha3/beta4 84.83% 97.23%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 84.80% 95.50%
CHEMBL3437 Q16853 Amine oxidase, copper containing 84.79% 94.00%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 84.79% 95.89%
CHEMBL5255 O00206 Toll-like receptor 4 84.71% 92.50%
CHEMBL5103 Q969S8 Histone deacetylase 10 83.94% 90.08%
CHEMBL1744525 P43490 Nicotinamide phosphoribosyltransferase 83.15% 96.25%
CHEMBL4296 Q15858 Sodium channel protein type IX alpha subunit 82.42% 96.11%
CHEMBL253 P34972 Cannabinoid CB2 receptor 82.34% 97.25%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 80.89% 93.03%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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Cross-Links

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PubChem 461349
LOTUS LTS0273638
wikiData Q77369041