H-Ile-D-Pro-Trp-Leu-NH2

Details

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Internal ID e29fff90-8e55-4d03-ad3b-5c8e16068774
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Amino acids, peptides, and analogues > Peptides
IUPAC Name (2R)-N-[(2S)-1-[[(2S)-1-amino-4-methyl-1-oxopentan-2-yl]amino]-3-(1H-indol-3-yl)-1-oxopropan-2-yl]-1-[(2S,3S)-2-amino-3-methylpentanoyl]pyrrolidine-2-carboxamide
SMILES (Canonical) CCC(C)C(C(=O)N1CCCC1C(=O)NC(CC2=CNC3=CC=CC=C32)C(=O)NC(CC(C)C)C(=O)N)N
SMILES (Isomeric) CC[C@H](C)[C@@H](C(=O)N1CCC[C@@H]1C(=O)N[C@@H](CC2=CNC3=CC=CC=C32)C(=O)N[C@@H](CC(C)C)C(=O)N)N
InChI InChI=1S/C28H42N6O4/c1-5-17(4)24(29)28(38)34-12-8-11-23(34)27(37)33-22(26(36)32-21(25(30)35)13-16(2)3)14-18-15-31-20-10-7-6-9-19(18)20/h6-7,9-10,15-17,21-24,31H,5,8,11-14,29H2,1-4H3,(H2,30,35)(H,32,36)(H,33,37)/t17-,21-,22-,23+,24-/m0/s1
InChI Key QFVMXUCLKWWRCB-LVTPPWGZSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C28H42N6O4
Molecular Weight 526.70 g/mol
Exact Mass 526.32675384 g/mol
Topological Polar Surface Area (TPSA) 163.00 Ų
XlogP 2.80
Atomic LogP (AlogP) 1.58
H-Bond Acceptor 5
H-Bond Donor 5
Rotatable Bonds 12

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of H-Ile-D-Pro-Trp-Leu-NH2

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9517 95.17%
Caco-2 - 0.8286 82.86%
Blood Brain Barrier - 0.8250 82.50%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Mitochondria 0.4291 42.91%
OATP2B1 inhibitior - 0.5733 57.33%
OATP1B1 inhibitior + 0.9119 91.19%
OATP1B3 inhibitior + 0.9412 94.12%
MATE1 inhibitior - 0.8267 82.67%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior + 0.9582 95.82%
P-glycoprotein inhibitior + 0.7490 74.90%
P-glycoprotein substrate + 0.8491 84.91%
CYP3A4 substrate + 0.6941 69.41%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7690 76.90%
CYP3A4 inhibition + 0.5812 58.12%
CYP2C9 inhibition - 0.7737 77.37%
CYP2C19 inhibition - 0.6144 61.44%
CYP2D6 inhibition - 0.9196 91.96%
CYP1A2 inhibition - 0.6126 61.26%
CYP2C8 inhibition - 0.5906 59.06%
CYP inhibitory promiscuity - 0.7487 74.87%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8300 83.00%
Carcinogenicity (trinary) Non-required 0.6706 67.06%
Eye corrosion - 0.9901 99.01%
Eye irritation - 0.9690 96.90%
Skin irritation - 0.7943 79.43%
Skin corrosion - 0.9260 92.60%
Ames mutagenesis - 0.7900 79.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7451 74.51%
Micronuclear + 0.7200 72.00%
Hepatotoxicity + 0.5625 56.25%
skin sensitisation - 0.9041 90.41%
Respiratory toxicity + 0.8222 82.22%
Reproductive toxicity + 0.9889 98.89%
Mitochondrial toxicity + 0.9125 91.25%
Nephrotoxicity - 0.8967 89.67%
Acute Oral Toxicity (c) III 0.6525 65.25%
Estrogen receptor binding + 0.6685 66.85%
Androgen receptor binding + 0.5521 55.21%
Thyroid receptor binding + 0.5439 54.39%
Glucocorticoid receptor binding + 0.6842 68.42%
Aromatase binding + 0.5607 56.07%
PPAR gamma + 0.6832 68.32%
Honey bee toxicity - 0.8630 86.30%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.7000 70.00%
Fish aquatic toxicity + 0.8968 89.68%

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
CHEMBL3837 P07711 Cathepsin L 99.82% 96.61%
CHEMBL2581 P07339 Cathepsin D 99.65% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 98.99% 96.09%
CHEMBL2693 Q9UIQ6 Cystinyl aminopeptidase 98.85% 97.64%
CHEMBL1795139 Q8IU80 Transmembrane protease serine 6 98.62% 98.33%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 98.57% 91.81%
CHEMBL3830 Q2M2I8 Adaptor-associated kinase 97.61% 83.10%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.20% 91.11%
CHEMBL3137262 O60341 LSD1/CoREST complex 95.81% 97.09%
CHEMBL333 P08253 Matrix metalloproteinase-2 94.89% 96.31%
CHEMBL4979 P13866 Sodium/glucose cotransporter 1 94.68% 98.24%
CHEMBL3310 Q96DB2 Histone deacetylase 11 94.66% 88.56%
CHEMBL3155 P34969 Serotonin 7 (5-HT7) receptor 94.40% 90.71%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.35% 95.56%
CHEMBL230 P35354 Cyclooxygenase-2 93.62% 89.63%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 92.97% 89.62%
CHEMBL221 P23219 Cyclooxygenase-1 92.82% 90.17%
CHEMBL2514 O95665 Neurotensin receptor 2 92.78% 100.00%
CHEMBL4123 P30989 Neurotensin receptor 1 91.27% 96.67%
CHEMBL321 P14780 Matrix metalloproteinase 9 90.93% 92.12%
CHEMBL4227 P25090 Lipoxin A4 receptor 90.35% 100.00%
CHEMBL4208 P20618 Proteasome component C5 89.82% 90.00%
CHEMBL213 P08588 Beta-1 adrenergic receptor 89.53% 95.56%
CHEMBL253 P34972 Cannabinoid CB2 receptor 89.12% 97.25%
CHEMBL3359 P21462 Formyl peptide receptor 1 89.10% 93.56%
CHEMBL2535 P11166 Glucose transporter 88.68% 98.75%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 88.09% 100.00%
CHEMBL4073 P09237 Matrix metalloproteinase 7 88.02% 97.56%
CHEMBL5608 Q16288 NT-3 growth factor receptor 88.01% 95.89%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 87.79% 96.95%
CHEMBL5939 Q9NZ08 Endoplasmic reticulum aminopeptidase 1 87.78% 100.00%
CHEMBL255 P29275 Adenosine A2b receptor 87.69% 98.59%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 87.37% 97.14%
CHEMBL5028 O14672 ADAM10 86.65% 97.50%
CHEMBL1944495 P28065 Proteasome subunit beta type-9 86.21% 97.50%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 86.11% 93.03%
CHEMBL259 P32245 Melanocortin receptor 4 86.03% 95.38%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 84.59% 96.47%
CHEMBL340 P08684 Cytochrome P450 3A4 84.51% 91.19%
CHEMBL3192 Q9BY41 Histone deacetylase 8 84.32% 93.99%
CHEMBL1808 P12821 Angiotensin-converting enzyme 84.00% 93.39%
CHEMBL2492 P36544 Neuronal acetylcholine receptor protein alpha-7 subunit 82.98% 88.42%
CHEMBL1806 P11388 DNA topoisomerase II alpha 82.95% 89.00%
CHEMBL5103 Q969S8 Histone deacetylase 10 82.71% 90.08%
CHEMBL1255126 O15151 Protein Mdm4 82.40% 90.20%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 82.25% 82.69%
CHEMBL4588 P22894 Matrix metalloproteinase 8 82.20% 94.66%
CHEMBL2107 P61073 C-X-C chemokine receptor type 4 81.93% 93.10%
CHEMBL4394 Q9NYA1 Sphingosine kinase 1 81.91% 96.03%
CHEMBL4816 Q9Y243 Serine/threonine-protein kinase AKT3 80.99% 96.28%
CHEMBL1907594 P30926 Neuronal acetylcholine receptor; alpha3/beta4 80.94% 97.23%
CHEMBL4051 P13569 Cystic fibrosis transmembrane conductance regulator 80.42% 95.71%

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 163191271
LOTUS LTS0174439
wikiData Q105219801