cyclo[D-Asn-His-Val-D-Asn-D-Phe-Pro-D-Pro-Thr-Phe]

Details

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Internal ID 7cb779ff-23e3-4cf8-ad12-983c46952083
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Amino acids, peptides, and analogues > Peptides > Cyclic peptides
IUPAC Name 2-[(3S,9R,12R,15S,18S,21R,24S,27S,30R)-12-(2-amino-2-oxoethyl)-9,24-dibenzyl-27-[(1R)-1-hydroxyethyl]-18-(1H-imidazol-5-ylmethyl)-2,8,11,14,17,20,23,26,29-nonaoxo-15-propan-2-yl-1,7,10,13,16,19,22,25,28-nonazatricyclo[28.3.0.03,7]tritriacontan-21-yl]acetamide
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C51H67N13O12/c1-27(2)41-48(73)59-35(24-40(53)67)45(70)60-36(21-30-14-8-5-9-15-30)50(75)64-19-11-17-38(64)51(76)63-18-10-16-37(63)47(72)62-42(28(3)65)49(74)58-32(20-29-12-6-4-7-13-29)43(68)57-34(23-39(52)66)44(69)56-33(46(71)61-41)22-31-25-54-26-55-31/h4-9,12-15,25-28,32-38,41-42,65H,10-11,16-24H2,1-3H3,(H2,52,66)(H2,53,67)(H,54,55)(H,56,69)(H,57,68)(H,58,74)(H,59,73)(H,60,70)(H,61,71)(H,62,72)/t28-,32+,33+,34-,35-,36-,37-,38+,41+,42+/m1/s1
InChI Key POVFXEIWKRHEKP-CJTJNDHGSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C51H67N13O12
Molecular Weight 1054.20 g/mol
Exact Mass 1053.50321462 g/mol
Topological Polar Surface Area (TPSA) 379.00 Ų
XlogP -0.90
Atomic LogP (AlogP) -3.39
H-Bond Acceptor 13
H-Bond Donor 11
Rotatable Bonds 12

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of cyclo[D-Asn-His-Val-D-Asn-D-Phe-Pro-D-Pro-Thr-Phe]

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.7565 75.65%
Caco-2 - 0.8702 87.02%
Blood Brain Barrier - 0.8500 85.00%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Mitochondria 0.6187 61.87%
OATP2B1 inhibitior - 0.5725 57.25%
OATP1B1 inhibitior + 0.8818 88.18%
OATP1B3 inhibitior + 0.9320 93.20%
MATE1 inhibitior - 0.9023 90.23%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior + 0.9394 93.94%
P-glycoprotein inhibitior + 0.7497 74.97%
P-glycoprotein substrate + 0.8235 82.35%
CYP3A4 substrate + 0.6578 65.78%
CYP2C9 substrate - 0.6070 60.70%
CYP2D6 substrate - 0.8384 83.84%
CYP3A4 inhibition - 0.8566 85.66%
CYP2C9 inhibition - 0.8722 87.22%
CYP2C19 inhibition - 0.8509 85.09%
CYP2D6 inhibition - 0.9256 92.56%
CYP1A2 inhibition - 0.9435 94.35%
CYP2C8 inhibition + 0.6003 60.03%
CYP inhibitory promiscuity - 0.9308 93.08%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.8700 87.00%
Carcinogenicity (trinary) Non-required 0.6081 60.81%
Eye corrosion - 0.9912 99.12%
Eye irritation - 0.9028 90.28%
Skin irritation - 0.8038 80.38%
Skin corrosion - 0.9382 93.82%
Ames mutagenesis - 0.7200 72.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6921 69.21%
Micronuclear + 0.8700 87.00%
Hepatotoxicity + 0.5234 52.34%
skin sensitisation - 0.9015 90.15%
Respiratory toxicity + 0.8778 87.78%
Reproductive toxicity + 0.9444 94.44%
Mitochondrial toxicity + 0.9250 92.50%
Nephrotoxicity - 0.7822 78.22%
Acute Oral Toxicity (c) III 0.6372 63.72%
Estrogen receptor binding + 0.7810 78.10%
Androgen receptor binding + 0.6993 69.93%
Thyroid receptor binding + 0.6161 61.61%
Glucocorticoid receptor binding + 0.5423 54.23%
Aromatase binding + 0.6442 64.42%
PPAR gamma + 0.7568 75.68%
Honey bee toxicity - 0.8496 84.96%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity - 0.6500 65.00%
Fish aquatic toxicity - 0.4612 46.12%

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
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 99.73% 85.14%
CHEMBL2581 P07339 Cathepsin D 99.63% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 99.52% 96.09%
CHEMBL2693 Q9UIQ6 Cystinyl aminopeptidase 98.00% 97.64%
CHEMBL4447 Q9Y337 Kallikrein 5 95.55% 87.50%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 95.53% 93.03%
CHEMBL5608 Q16288 NT-3 growth factor receptor 95.28% 95.89%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 94.28% 94.45%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.21% 95.56%
CHEMBL221 P23219 Cyclooxygenase-1 92.08% 90.17%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 90.15% 93.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 89.38% 97.09%
CHEMBL5103 Q969S8 Histone deacetylase 10 89.28% 90.08%
CHEMBL4071 P08311 Cathepsin G 86.01% 94.64%
CHEMBL2443 P49862 Kallikrein 7 85.47% 94.00%
CHEMBL213 P08588 Beta-1 adrenergic receptor 83.83% 95.56%
CHEMBL2069156 Q14145 Kelch-like ECH-associated protein 1 83.67% 82.38%
CHEMBL1293249 Q13887 Kruppel-like factor 5 82.83% 86.33%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.68% 99.23%
CHEMBL3202 P48147 Prolyl endopeptidase 80.45% 90.65%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 80.22% 90.71%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
Annona montana

Cross-Links

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PubChem 162964168
LOTUS LTS0146033
wikiData Q105212697