Microcin C7

Details

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Internal ID dd436485-eb22-450c-b878-8894a1bab555
Taxonomy Organic acids and derivatives > Peptidomimetics > Hybrid peptides > Hybrid glycopeptides
IUPAC Name [[(2S)-2-[[(2S)-2-[[(2S)-4-amino-2-[[2-[[(2S,3R)-2-[[(2S)-5-(diaminomethylideneamino)-2-[[(2S)-2-formamido-4-methylsulfanylbutanoyl]amino]pentanoyl]amino]-3-hydroxybutanoyl]amino]acetyl]amino]-4-oxobutanoyl]amino]propanoyl]amino]-3-carboxypropanoyl]amino]-(3-aminopropoxy)-[[(2R,3S,4R,5R)-5-(6-aminopurin-9-yl)-3,4-dihydroxyoxolan-2-yl]methoxy]-hydroxyphosphanium
SMILES (Canonical) CC(C(C(=O)NCC(=O)NC(CC(=O)N)C(=O)NC(C)C(=O)NC(CC(=O)O)C(=O)N[P+](O)(OCCCN)OCC1C(C(C(O1)N2C=NC3=C(N=CN=C32)N)O)O)NC(=O)C(CCCN=C(N)N)NC(=O)C(CCSC)NC=O)O
SMILES (Isomeric) C[C@H]([C@@H](C(=O)NCC(=O)N[C@@H](CC(=O)N)C(=O)N[C@@H](C)C(=O)N[C@@H](CC(=O)O)C(=O)N[P+](O)(OCCCN)OC[C@@H]1[C@H]([C@H]([C@@H](O1)N2C=NC3=C(N=CN=C32)N)O)O)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CCSC)NC=O)O
InChI InChI=1S/C42H69N18O18PS/c1-19(35(69)57-24(13-28(65)66)39(73)59-79(75,76-10-5-8-43)77-15-25-31(67)32(68)41(78-25)60-17-52-30-33(45)50-16-51-34(30)60)54-38(72)23(12-26(44)63)55-27(64)14-49-40(74)29(20(2)62)58-37(71)22(6-4-9-48-42(46)47)56-36(70)21(53-18-61)7-11-80-3/h16-25,29,31-32,41,62,67-68,75H,4-15,43H2,1-3H3,(H16-,44,45,46,47,48,49,50,51,53,54,55,56,57,58,59,61,63,64,65,66,69,70,71,72,73,74)/p+1/t19-,20+,21-,22-,23-,24-,25+,29-,31+,32+,41+,79?/m0/s1
InChI Key HPVDPNOXNZKNAU-CRNXWWIHSA-O
Popularity 405 references in papers

Physical and Chemical Properties

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Molecular Formula C42H70N18O18PS+
Molecular Weight 1178.20 g/mol
Exact Mass 1177.45738063 g/mol
Topological Polar Surface Area (TPSA) 607.00 Ų
XlogP -11.50
Atomic LogP (AlogP) -8.59
H-Bond Acceptor 25
H-Bond Donor 18
Rotatable Bonds 36

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Microcin C7

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.5193 51.93%
Caco-2 - 0.8614 86.14%
Blood Brain Barrier - 0.6750 67.50%
Human oral bioavailability - 0.7571 75.71%
Subcellular localzation Lysosomes 0.3290 32.90%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8075 80.75%
OATP1B3 inhibitior + 0.9313 93.13%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.5811 58.11%
BSEP inhibitior + 0.9413 94.13%
P-glycoprotein inhibitior + 0.7422 74.22%
P-glycoprotein substrate + 0.8476 84.76%
CYP3A4 substrate + 0.7397 73.97%
CYP2C9 substrate - 0.5969 59.69%
CYP2D6 substrate - 0.8463 84.63%
CYP3A4 inhibition - 0.9024 90.24%
CYP2C9 inhibition - 0.7928 79.28%
CYP2C19 inhibition - 0.7927 79.27%
CYP2D6 inhibition - 0.8411 84.11%
CYP1A2 inhibition - 0.7186 71.86%
CYP2C8 inhibition + 0.8144 81.44%
CYP inhibitory promiscuity - 0.9717 97.17%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.8600 86.00%
Carcinogenicity (trinary) Non-required 0.5241 52.41%
Eye corrosion - 0.9789 97.89%
Eye irritation - 0.8963 89.63%
Skin irritation - 0.7528 75.28%
Skin corrosion - 0.9155 91.55%
Ames mutagenesis - 0.6100 61.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6743 67.43%
Micronuclear + 0.9000 90.00%
Hepatotoxicity - 0.6602 66.02%
skin sensitisation - 0.8244 82.44%
Respiratory toxicity + 0.7889 78.89%
Reproductive toxicity + 0.9333 93.33%
Mitochondrial toxicity + 0.9250 92.50%
Nephrotoxicity - 0.6440 64.40%
Acute Oral Toxicity (c) III 0.5402 54.02%
Estrogen receptor binding + 0.5799 57.99%
Androgen receptor binding + 0.7164 71.64%
Thyroid receptor binding + 0.6596 65.96%
Glucocorticoid receptor binding + 0.7353 73.53%
Aromatase binding + 0.7676 76.76%
PPAR gamma + 0.6929 69.29%
Honey bee toxicity - 0.6695 66.95%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.6900 69.00%
Fish aquatic toxicity + 0.6987 69.87%

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
CHEMBL4040 P28482 MAP kinase ERK2 99.99% 83.82%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 99.75% 96.09%
CHEMBL2581 P07339 Cathepsin D 99.62% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 99.10% 91.11%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 99.09% 96.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 98.25% 99.17%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 97.52% 94.45%
CHEMBL221 P23219 Cyclooxygenase-1 96.72% 90.17%
CHEMBL2492 P36544 Neuronal acetylcholine receptor protein alpha-7 subunit 96.68% 88.42%
CHEMBL2107 P61073 C-X-C chemokine receptor type 4 94.86% 93.10%
CHEMBL3776 Q14790 Caspase-8 94.39% 97.06%
CHEMBL1795139 Q8IU80 Transmembrane protease serine 6 94.10% 98.33%
CHEMBL3401 O75469 Pregnane X receptor 92.95% 94.73%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 92.88% 100.00%
CHEMBL1255126 O15151 Protein Mdm4 92.72% 90.20%
CHEMBL1075162 Q13304 Uracil nucleotide/cysteinyl leukotriene receptor 92.41% 80.33%
CHEMBL5163 Q9NY46 Sodium channel protein type III alpha subunit 91.75% 96.90%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 91.59% 93.00%
CHEMBL2514 O95665 Neurotensin receptor 2 91.28% 100.00%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 90.50% 90.71%
CHEMBL2094135 Q96BI3 Gamma-secretase 90.32% 98.05%
CHEMBL2535 P11166 Glucose transporter 88.70% 98.75%
CHEMBL2243 O00519 Anandamide amidohydrolase 88.44% 97.53%
CHEMBL230 P35354 Cyclooxygenase-2 88.02% 89.63%
CHEMBL2069156 Q14145 Kelch-like ECH-associated protein 1 87.56% 82.38%
CHEMBL3359 P21462 Formyl peptide receptor 1 86.81% 93.56%
CHEMBL5608 Q16288 NT-3 growth factor receptor 86.68% 95.89%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 86.67% 100.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.16% 95.56%
CHEMBL1907594 P30926 Neuronal acetylcholine receptor; alpha3/beta4 86.13% 97.23%
CHEMBL3286 P00749 Urokinase-type plasminogen activator 85.70% 97.88%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 85.59% 95.89%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.57% 86.33%
CHEMBL3979 Q03181 Peroxisome proliferator-activated receptor delta 85.31% 93.95%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 85.16% 96.47%
CHEMBL3004 P33527 Multidrug resistance-associated protein 1 84.75% 96.37%
CHEMBL3308 P55212 Caspase-6 84.69% 97.56%
CHEMBL3137261 O14744 PRMT5/MEP50 complex 84.14% 100.00%
CHEMBL3891 P07384 Calpain 1 83.87% 93.04%
CHEMBL259 P32245 Melanocortin receptor 4 83.10% 95.38%
CHEMBL2095164 P49354 Geranylgeranyl transferase type I 81.90% 92.80%
CHEMBL5028 O14672 ADAM10 81.11% 97.50%
CHEMBL1806 P11388 DNA topoisomerase II alpha 80.86% 89.00%
CHEMBL1881 P43116 Prostanoid EP2 receptor 80.75% 93.00%

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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There are no matching plants.

Cross-Links

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PubChem 145720574
LOTUS LTS0008148
wikiData Q105031900