cyclo[Asn-Pro-Phe-Ile-Leu-Pro-Val]

Details

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Internal ID d12ae610-d361-4f74-a2fb-181c38044e60
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Amino acids, peptides, and analogues > Peptides > Oligopeptides
IUPAC Name 2-[(3S,6S,9S,15S,18S,21S,24S)-21-benzyl-18-[(2S)-butan-2-yl]-15-(2-methylpropyl)-2,5,8,14,17,20,23-heptaoxo-6-propan-2-yl-1,4,7,13,16,19,22-heptazatricyclo[22.3.0.09,13]heptacosan-3-yl]acetamide
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C40H60N8O8/c1-7-24(6)33-38(54)43-27(19-22(2)3)39(55)48-18-12-16-30(48)36(52)45-32(23(4)5)37(53)44-28(21-31(41)49)40(56)47-17-11-15-29(47)35(51)42-26(34(50)46-33)20-25-13-9-8-10-14-25/h8-10,13-14,22-24,26-30,32-33H,7,11-12,15-21H2,1-6H3,(H2,41,49)(H,42,51)(H,43,54)(H,44,53)(H,45,52)(H,46,50)/t24-,26-,27-,28-,29-,30-,32-,33-/m0/s1
InChI Key ANLDPEXRVVIABH-FHQZTVGNSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C40H60N8O8
Molecular Weight 781.00 g/mol
Exact Mass 780.45341090 g/mol
Topological Polar Surface Area (TPSA) 229.00 Ų
XlogP 2.50
Atomic LogP (AlogP) 0.27
H-Bond Acceptor 8
H-Bond Donor 6
Rotatable Bonds 9

Synonyms

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CHEMBL1793965

2D Structure

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2D Structure of cyclo[Asn-Pro-Phe-Ile-Leu-Pro-Val]

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8848 88.48%
Caco-2 - 0.8559 85.59%
Blood Brain Barrier - 0.7500 75.00%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Lysosomes 0.4530 45.30%
OATP2B1 inhibitior + 0.5610 56.10%
OATP1B1 inhibitior + 0.8966 89.66%
OATP1B3 inhibitior + 0.9366 93.66%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior + 0.9509 95.09%
P-glycoprotein inhibitior + 0.7772 77.72%
P-glycoprotein substrate + 0.8503 85.03%
CYP3A4 substrate + 0.6289 62.89%
CYP2C9 substrate - 0.5975 59.75%
CYP2D6 substrate - 0.8107 81.07%
CYP3A4 inhibition - 0.9560 95.60%
CYP2C9 inhibition - 0.8679 86.79%
CYP2C19 inhibition - 0.8608 86.08%
CYP2D6 inhibition - 0.9200 92.00%
CYP1A2 inhibition - 0.9162 91.62%
CYP2C8 inhibition - 0.6070 60.70%
CYP inhibitory promiscuity - 0.9701 97.01%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8500 85.00%
Carcinogenicity (trinary) Non-required 0.6746 67.46%
Eye corrosion - 0.9890 98.90%
Eye irritation - 0.9214 92.14%
Skin irritation - 0.7858 78.58%
Skin corrosion - 0.9155 91.55%
Ames mutagenesis - 0.7300 73.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3732 37.32%
Micronuclear + 0.8200 82.00%
Hepatotoxicity + 0.5854 58.54%
skin sensitisation - 0.8867 88.67%
Respiratory toxicity + 0.8444 84.44%
Reproductive toxicity + 0.8667 86.67%
Mitochondrial toxicity + 0.8375 83.75%
Nephrotoxicity - 0.6817 68.17%
Acute Oral Toxicity (c) III 0.6001 60.01%
Estrogen receptor binding + 0.8077 80.77%
Androgen receptor binding + 0.6834 68.34%
Thyroid receptor binding + 0.5452 54.52%
Glucocorticoid receptor binding + 0.6244 62.44%
Aromatase binding + 0.6495 64.95%
PPAR gamma + 0.7648 76.48%
Honey bee toxicity - 0.8823 88.23%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.5600 56.00%
Fish aquatic toxicity + 0.7617 76.17%

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 99.83% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 99.19% 96.09%
CHEMBL221 P23219 Cyclooxygenase-1 97.00% 90.17%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.55% 95.56%
CHEMBL2693 Q9UIQ6 Cystinyl aminopeptidase 95.19% 97.64%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 94.60% 85.14%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 93.16% 93.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 92.93% 97.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 91.39% 94.45%
CHEMBL5608 Q16288 NT-3 growth factor receptor 91.21% 95.89%
CHEMBL2069156 Q14145 Kelch-like ECH-associated protein 1 90.80% 82.38%
CHEMBL3392948 Q9NP59 Solute carrier family 40 member 1 89.69% 95.00%
CHEMBL5103 Q969S8 Histone deacetylase 10 88.66% 90.08%
CHEMBL253 P34972 Cannabinoid CB2 receptor 87.32% 97.25%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 87.29% 91.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.80% 86.33%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 86.79% 93.03%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 84.42% 96.47%
CHEMBL4071 P08311 Cathepsin G 82.82% 94.64%
CHEMBL4394 Q9NYA1 Sphingosine kinase 1 82.45% 96.03%
CHEMBL4523377 Q86WV6 Stimulator of interferon genes protein 82.12% 95.48%
CHEMBL333 P08253 Matrix metalloproteinase-2 81.51% 96.31%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 81.27% 97.14%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 81.18% 90.71%
CHEMBL2443 P49862 Kallikrein 7 80.43% 94.00%

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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Cross-Links

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PubChem 6914804
LOTUS LTS0003610
wikiData Q104915259