(D-Leu1,D-Asp3)MC-LR

Details

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Internal ID 816acf5a-4ed7-42a2-940d-cde93e54be24
Taxonomy Organic acids and derivatives > Peptidomimetics > Hybrid peptides
IUPAC Name (5R,8S,11R,15S,18S,19S,22R)-15-[3-(diaminomethylideneamino)propyl]-18-[(1E,3E,5S,6S)-6-methoxy-3,5-dimethyl-7-phenylhepta-1,3-dienyl]-1,19-dimethyl-2-methylidene-5,8-bis(2-methylpropyl)-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/C51H78N10O12/c1-28(2)23-38-47(67)59-39(24-29(3)4)48(68)60-40(50(71)72)27-42(62)55-36(17-14-22-54-51(52)53)46(66)56-35(19-18-30(5)25-31(6)41(73-10)26-34-15-12-11-13-16-34)32(7)44(64)57-37(49(69)70)20-21-43(63)61(9)33(8)45(65)58-38/h11-13,15-16,18-19,25,28-29,31-32,35-41H,8,14,17,20-24,26-27H2,1-7,9-10H3,(H,55,62)(H,56,66)(H,57,64)(H,58,65)(H,59,67)(H,60,68)(H,69,70)(H,71,72)(H4,52,53,54)/b19-18+,30-25+/t31-,32-,35-,36-,37+,38+,39-,40+,41-/m0/s1
InChI Key AVSMHCMQBTVLHC-IBQQIYNOSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C51H78N10O12
Molecular Weight 1023.20 g/mol
Exact Mass 1022.58006796 g/mol
Topological Polar Surface Area (TPSA) 343.00 Ų
XlogP 3.10
Atomic LogP (AlogP) 1.40
H-Bond Acceptor 11
H-Bond Donor 10
Rotatable Bonds 17

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (D-Leu1,D-Asp3)MC-LR

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.5514 55.14%
Caco-2 - 0.8647 86.47%
Blood Brain Barrier - 0.8000 80.00%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.6563 65.63%
OATP2B1 inhibitior - 0.8559 85.59%
OATP1B1 inhibitior + 0.8231 82.31%
OATP1B3 inhibitior + 0.9199 91.99%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior + 0.9225 92.25%
P-glycoprotein inhibitior + 0.7463 74.63%
P-glycoprotein substrate + 0.8691 86.91%
CYP3A4 substrate + 0.7355 73.55%
CYP2C9 substrate + 0.5767 57.67%
CYP2D6 substrate - 0.8663 86.63%
CYP3A4 inhibition - 0.8093 80.93%
CYP2C9 inhibition - 0.7209 72.09%
CYP2C19 inhibition - 0.6981 69.81%
CYP2D6 inhibition - 0.8869 88.69%
CYP1A2 inhibition - 0.7587 75.87%
CYP2C8 inhibition + 0.7445 74.45%
CYP inhibitory promiscuity - 0.9406 94.06%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8500 85.00%
Carcinogenicity (trinary) Non-required 0.6042 60.42%
Eye corrosion - 0.9819 98.19%
Eye irritation - 0.9000 90.00%
Skin irritation - 0.7595 75.95%
Skin corrosion - 0.9181 91.81%
Ames mutagenesis - 0.6300 63.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7187 71.87%
Micronuclear + 0.8100 81.00%
Hepatotoxicity + 0.5302 53.02%
skin sensitisation - 0.8306 83.06%
Respiratory toxicity + 0.8222 82.22%
Reproductive toxicity + 0.8444 84.44%
Mitochondrial toxicity + 0.8125 81.25%
Nephrotoxicity - 0.7566 75.66%
Acute Oral Toxicity (c) I 0.7449 74.49%
Estrogen receptor binding + 0.7446 74.46%
Androgen receptor binding + 0.7284 72.84%
Thyroid receptor binding + 0.6372 63.72%
Glucocorticoid receptor binding + 0.6651 66.51%
Aromatase binding + 0.6564 65.64%
PPAR gamma + 0.7958 79.58%
Honey bee toxicity - 0.6816 68.16%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.5000 50.00%
Fish aquatic toxicity + 0.9102 91.02%

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 99.98% 83.82%
CHEMBL2581 P07339 Cathepsin D 99.88% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 99.61% 96.09%
CHEMBL3837 P07711 Cathepsin L 98.43% 96.61%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 96.36% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 95.70% 86.33%
CHEMBL3060 Q9Y345 Glycine transporter 2 94.12% 99.17%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.03% 91.11%
CHEMBL4072 P07858 Cathepsin B 93.50% 93.67%
CHEMBL2693 Q9UIQ6 Cystinyl aminopeptidase 93.18% 97.64%
CHEMBL5608 Q16288 NT-3 growth factor receptor 92.20% 95.89%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 90.19% 90.71%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 90.02% 94.45%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 89.28% 91.71%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 88.77% 95.89%
CHEMBL3137262 O60341 LSD1/CoREST complex 87.56% 97.09%
CHEMBL1255126 O15151 Protein Mdm4 85.85% 90.20%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 85.77% 82.69%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 85.64% 93.00%
CHEMBL5103 Q969S8 Histone deacetylase 10 85.29% 90.08%
CHEMBL4644 P41968 Melanocortin receptor 3 83.60% 99.52%
CHEMBL2535 P11166 Glucose transporter 83.24% 98.75%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 81.72% 100.00%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 81.07% 96.47%
CHEMBL1937 Q92769 Histone deacetylase 2 80.25% 94.75%

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 146683869
LOTUS LTS0117790
wikiData Q104246590