cyclo[DL-Ala-DL-Pro-DL-Leu-DL-Pro-DL-Phe-DL-Pro-DL-Phe-DL-Phe]

Details

Top
Internal ID 9325a2f0-e8ed-4fd2-8591-727dfe248b5e
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Amino acids, peptides, and analogues > Peptides > Oligopeptides
IUPAC Name 3,24,27-tribenzyl-21-methyl-12-(2-methylpropyl)-1,4,10,13,19,22,25,28-octazatetracyclo[28.3.0.06,10.015,19]tritriacontane-2,5,11,14,20,23,26,29-octone
SMILES (Canonical) CC1C(=O)N2CCCC2C(=O)NC(C(=O)N3CCCC3C(=O)NC(C(=O)N4CCCC4C(=O)NC(C(=O)NC(C(=O)N1)CC5=CC=CC=C5)CC6=CC=CC=C6)CC7=CC=CC=C7)CC(C)C
SMILES (Isomeric) CC1C(=O)N2CCCC2C(=O)NC(C(=O)N3CCCC3C(=O)NC(C(=O)N4CCCC4C(=O)NC(C(=O)NC(C(=O)N1)CC5=CC=CC=C5)CC6=CC=CC=C6)CC7=CC=CC=C7)CC(C)C
InChI InChI=1S/C51H64N8O8/c1-32(2)28-39-50(66)58-26-15-24-43(58)48(64)56-40(31-36-20-11-6-12-21-36)51(67)59-27-14-23-42(59)46(62)54-38(30-35-18-9-5-10-19-35)45(61)53-37(29-34-16-7-4-8-17-34)44(60)52-33(3)49(65)57-25-13-22-41(57)47(63)55-39/h4-12,16-21,32-33,37-43H,13-15,22-31H2,1-3H3,(H,52,60)(H,53,61)(H,54,62)(H,55,63)(H,56,64)
InChI Key NTDOASLXLMRACR-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

Top
Molecular Formula C51H64N8O8
Molecular Weight 917.10 g/mol
Exact Mass 916.48471103 g/mol
Topological Polar Surface Area (TPSA) 206.00 Ų
XlogP 5.00
Atomic LogP (AlogP) 2.19
H-Bond Acceptor 8
H-Bond Donor 5
Rotatable Bonds 8

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of cyclo[DL-Ala-DL-Pro-DL-Leu-DL-Pro-DL-Phe-DL-Pro-DL-Phe-DL-Phe]

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.7949 79.49%
Caco-2 - 0.8713 87.13%
Blood Brain Barrier - 0.9000 90.00%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Mitochondria 0.6025 60.25%
OATP2B1 inhibitior - 0.5687 56.87%
OATP1B1 inhibitior + 0.9015 90.15%
OATP1B3 inhibitior + 0.9332 93.32%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8814 88.14%
BSEP inhibitior + 0.9570 95.70%
P-glycoprotein inhibitior + 0.7812 78.12%
P-glycoprotein substrate + 0.8002 80.02%
CYP3A4 substrate + 0.5800 58.00%
CYP2C9 substrate - 0.6180 61.80%
CYP2D6 substrate - 0.7959 79.59%
CYP3A4 inhibition - 0.7673 76.73%
CYP2C9 inhibition - 0.6787 67.87%
CYP2C19 inhibition - 0.6710 67.10%
CYP2D6 inhibition - 0.8828 88.28%
CYP1A2 inhibition - 0.9570 95.70%
CYP2C8 inhibition - 0.8009 80.09%
CYP inhibitory promiscuity - 0.9117 91.17%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8600 86.00%
Carcinogenicity (trinary) Non-required 0.6475 64.75%
Eye corrosion - 0.9918 99.18%
Eye irritation - 0.9136 91.36%
Skin irritation - 0.7964 79.64%
Skin corrosion - 0.9322 93.22%
Ames mutagenesis - 0.6600 66.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7014 70.14%
Micronuclear + 0.7200 72.00%
Hepatotoxicity + 0.6250 62.50%
skin sensitisation - 0.9144 91.44%
Respiratory toxicity + 0.8667 86.67%
Reproductive toxicity + 0.8889 88.89%
Mitochondrial toxicity + 0.9375 93.75%
Nephrotoxicity - 0.6324 63.24%
Acute Oral Toxicity (c) III 0.7177 71.77%
Estrogen receptor binding + 0.8151 81.51%
Androgen receptor binding + 0.6923 69.23%
Thyroid receptor binding + 0.5827 58.27%
Glucocorticoid receptor binding + 0.6443 64.43%
Aromatase binding + 0.5619 56.19%
PPAR gamma + 0.7769 77.69%
Honey bee toxicity - 0.9032 90.32%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.5600 56.00%
Fish aquatic toxicity + 0.9656 96.56%

Targets

Top

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 99.85% 98.95%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 96.44% 85.14%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.20% 96.09%
CHEMBL3524 P56524 Histone deacetylase 4 95.34% 92.97%
CHEMBL2693 Q9UIQ6 Cystinyl aminopeptidase 95.09% 97.64%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.56% 95.56%
CHEMBL333 P08253 Matrix metalloproteinase-2 92.13% 96.31%
CHEMBL253 P34972 Cannabinoid CB2 receptor 90.16% 97.25%
CHEMBL1902 P62942 FK506-binding protein 1A 89.53% 97.05%
CHEMBL5103 Q969S8 Histone deacetylase 10 89.53% 90.08%
CHEMBL5608 Q16288 NT-3 growth factor receptor 88.00% 95.89%
CHEMBL2069156 Q14145 Kelch-like ECH-associated protein 1 87.93% 82.38%
CHEMBL3137262 O60341 LSD1/CoREST complex 86.72% 97.09%
CHEMBL3202 P48147 Prolyl endopeptidase 85.68% 90.65%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 85.25% 97.14%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.92% 86.33%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 84.67% 93.00%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 83.74% 93.03%
CHEMBL264 Q9Y5N1 Histamine H3 receptor 83.18% 91.43%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 82.31% 90.71%
CHEMBL221 P23219 Cyclooxygenase-1 81.89% 90.17%
CHEMBL5966 P55899 IgG receptor FcRn large subunit p51 81.74% 90.93%

Plants that contains it

Top
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.
Psammosilene tunicoides

Cross-Links

Top
PubChem 5320752
NPASS NPC175359
LOTUS LTS0248879
wikiData Q105185396