(Gly1,D-Asp3,ADMAdda5)MC-RR

Details

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Internal ID f84ea5e9-5ccd-4e6f-a091-aa2962b95f74
Taxonomy Organic acids and derivatives > Peptidomimetics > Hybrid peptides
IUPAC Name (8S,11R,15S,18S,19S,22R)-18-[(1E,3E,5S,6S)-6-acetyloxy-3,5-dimethyl-7-phenylhepta-1,3-dienyl]-8,15-bis[3-(diaminomethylideneamino)propyl]-1,19-dimethyl-2-methylidene-3,6,9,13,16,20,25-heptaoxo-1,4,7,10,14,17,21-heptazacyclopentacosane-11,22-dicarboxylic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C48H71N13O13/c1-26(22-27(2)37(74-30(5)62)23-31-12-8-7-9-13-31)16-17-32-28(3)41(66)59-35(45(70)71)18-19-40(65)61(6)29(4)42(67)55-25-39(64)57-34(15-11-21-54-48(51)52)44(69)60-36(46(72)73)24-38(63)56-33(43(68)58-32)14-10-20-53-47(49)50/h7-9,12-13,16-17,22,27-28,32-37H,4,10-11,14-15,18-21,23-25H2,1-3,5-6H3,(H,55,67)(H,56,63)(H,57,64)(H,58,68)(H,59,66)(H,60,69)(H,70,71)(H,72,73)(H4,49,50,53)(H4,51,52,54)/b17-16+,26-22+/t27-,28-,32-,33-,34-,35+,36+,37-/m0/s1
InChI Key UBDNPCAZTHQJTO-KTRJARRNSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C48H71N13O13
Molecular Weight 1038.20 g/mol
Exact Mass 1037.52942937 g/mol
Topological Polar Surface Area (TPSA) 425.00 Ų
XlogP -1.20
Atomic LogP (AlogP) -2.09
H-Bond Acceptor 13
H-Bond Donor 12
Rotatable Bonds 17

Synonyms

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DTXSID301334596

2D Structure

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2D Structure of (Gly1,D-Asp3,ADMAdda5)MC-RR

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.6282 62.82%
Caco-2 - 0.8629 86.29%
Blood Brain Barrier - 0.7250 72.50%
Human oral bioavailability - 0.6429 64.29%
Subcellular localzation Mitochondria 0.6597 65.97%
OATP2B1 inhibitior - 0.8578 85.78%
OATP1B1 inhibitior + 0.8249 82.49%
OATP1B3 inhibitior + 0.9274 92.74%
MATE1 inhibitior - 0.7800 78.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior + 0.8906 89.06%
P-glycoprotein inhibitior + 0.7457 74.57%
P-glycoprotein substrate + 0.8649 86.49%
CYP3A4 substrate + 0.7348 73.48%
CYP2C9 substrate - 0.6215 62.15%
CYP2D6 substrate - 0.8724 87.24%
CYP3A4 inhibition - 0.9134 91.34%
CYP2C9 inhibition - 0.7295 72.95%
CYP2C19 inhibition - 0.7488 74.88%
CYP2D6 inhibition - 0.8829 88.29%
CYP1A2 inhibition - 0.7610 76.10%
CYP2C8 inhibition + 0.7515 75.15%
CYP inhibitory promiscuity - 0.9537 95.37%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8800 88.00%
Carcinogenicity (trinary) Non-required 0.5913 59.13%
Eye corrosion - 0.9824 98.24%
Eye irritation - 0.8991 89.91%
Skin irritation - 0.7572 75.72%
Skin corrosion - 0.9211 92.11%
Ames mutagenesis - 0.6200 62.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6882 68.82%
Micronuclear + 0.8300 83.00%
Hepatotoxicity + 0.5427 54.27%
skin sensitisation - 0.8332 83.32%
Respiratory toxicity + 0.7444 74.44%
Reproductive toxicity + 0.8556 85.56%
Mitochondrial toxicity + 0.8125 81.25%
Nephrotoxicity - 0.7055 70.55%
Acute Oral Toxicity (c) I 0.4852 48.52%
Estrogen receptor binding + 0.7035 70.35%
Androgen receptor binding + 0.7058 70.58%
Thyroid receptor binding + 0.6506 65.06%
Glucocorticoid receptor binding + 0.6470 64.70%
Aromatase binding + 0.6930 69.30%
PPAR gamma + 0.7412 74.12%
Honey bee toxicity - 0.6865 68.65%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity + 0.5300 53.00%
Fish aquatic toxicity - 0.3694 36.94%

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 99.95% 83.82%
CHEMBL2581 P07339 Cathepsin D 99.88% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 99.62% 96.09%
CHEMBL3837 P07711 Cathepsin L 98.00% 96.61%
CHEMBL2693 Q9UIQ6 Cystinyl aminopeptidase 95.00% 97.64%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.87% 95.56%
CHEMBL4072 P07858 Cathepsin B 94.19% 93.67%
CHEMBL1293249 Q13887 Kruppel-like factor 5 94.14% 86.33%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.73% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 92.98% 94.45%
CHEMBL3060 Q9Y345 Glycine transporter 2 92.98% 99.17%
CHEMBL5608 Q16288 NT-3 growth factor receptor 91.00% 95.89%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 89.44% 90.71%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 86.89% 95.89%
CHEMBL5103 Q969S8 Histone deacetylase 10 85.98% 90.08%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 85.83% 82.69%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 85.74% 93.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 84.91% 89.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 84.31% 97.09%
CHEMBL255 P29275 Adenosine A2b receptor 84.24% 98.59%
CHEMBL226 P30542 Adenosine A1 receptor 83.47% 95.93%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 83.18% 100.00%
CHEMBL2535 P11166 Glucose transporter 83.05% 98.75%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 82.60% 91.71%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 82.33% 85.14%

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 146683838
LOTUS LTS0183641
wikiData Q105269237