Calcaripeptide C

Details

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Internal ID 7a7ee6e9-f5d5-4a8c-8fae-bb389282fbc9
Taxonomy Organic acids and derivatives > Peptidomimetics > Depsipeptides > Cyclic depsipeptides
IUPAC Name (3S,6S,8R,11R,14S)-3-benzyl-6,8,11-trimethyl-12-oxa-1,4-diazabicyclo[12.3.0]heptadecane-2,5,7,13-tetrone
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C24H32N2O5/c1-15-11-12-16(2)31-24(30)20-10-7-13-26(20)23(29)19(14-18-8-5-4-6-9-18)25-22(28)17(3)21(15)27/h4-6,8-9,15-17,19-20H,7,10-14H2,1-3H3,(H,25,28)/t15-,16-,17+,19+,20+/m1/s1
InChI Key JFXPTGJYLLVAFU-JOMPHRNESA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C24H32N2O5
Molecular Weight 428.50 g/mol
Exact Mass 428.23112213 g/mol
Topological Polar Surface Area (TPSA) 92.80 Ų
XlogP 3.40
Atomic LogP (AlogP) 2.27
H-Bond Acceptor 5
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Calcaripeptide C

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9103 91.03%
Caco-2 - 0.5486 54.86%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Lysosomes 0.4790 47.90%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8355 83.55%
OATP1B3 inhibitior + 0.9138 91.38%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior + 0.6586 65.86%
P-glycoprotein inhibitior + 0.8507 85.07%
P-glycoprotein substrate + 0.7170 71.70%
CYP3A4 substrate + 0.6146 61.46%
CYP2C9 substrate - 0.5779 57.79%
CYP2D6 substrate - 0.8073 80.73%
CYP3A4 inhibition - 0.8427 84.27%
CYP2C9 inhibition - 0.9155 91.55%
CYP2C19 inhibition - 0.7744 77.44%
CYP2D6 inhibition - 0.9156 91.56%
CYP1A2 inhibition - 0.8687 86.87%
CYP2C8 inhibition - 0.7048 70.48%
CYP inhibitory promiscuity - 0.8258 82.58%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.6448 64.48%
Eye corrosion - 0.9925 99.25%
Eye irritation - 0.9887 98.87%
Skin irritation - 0.8133 81.33%
Skin corrosion - 0.9369 93.69%
Ames mutagenesis - 0.6500 65.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7876 78.76%
Micronuclear + 0.6900 69.00%
Hepatotoxicity + 0.6466 64.66%
skin sensitisation - 0.9046 90.46%
Respiratory toxicity + 0.8444 84.44%
Reproductive toxicity + 0.8111 81.11%
Mitochondrial toxicity + 0.9000 90.00%
Nephrotoxicity - 0.6103 61.03%
Acute Oral Toxicity (c) III 0.7099 70.99%
Estrogen receptor binding - 0.5443 54.43%
Androgen receptor binding + 0.6772 67.72%
Thyroid receptor binding - 0.5952 59.52%
Glucocorticoid receptor binding + 0.5477 54.77%
Aromatase binding - 0.7328 73.28%
PPAR gamma - 0.5000 50.00%
Honey bee toxicity - 0.8971 89.71%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity + 0.5100 51.00%
Fish aquatic toxicity + 0.8868 88.68%

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
CHEMBL2581 P07339 Cathepsin D 99.24% 98.95%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 97.69% 85.14%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.08% 96.09%
CHEMBL2693 Q9UIQ6 Cystinyl aminopeptidase 95.06% 97.64%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.49% 95.56%
CHEMBL2069156 Q14145 Kelch-like ECH-associated protein 1 93.71% 82.38%
CHEMBL1902 P62942 FK506-binding protein 1A 93.27% 97.05%
CHEMBL5608 Q16288 NT-3 growth factor receptor 89.70% 95.89%
CHEMBL5103 Q969S8 Histone deacetylase 10 87.28% 90.08%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 87.24% 93.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 86.23% 97.09%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 86.08% 93.03%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.83% 86.33%
CHEMBL3524 P56524 Histone deacetylase 4 84.60% 92.97%
CHEMBL4523377 Q86WV6 Stimulator of interferon genes protein 82.58% 95.48%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 81.74% 97.14%
CHEMBL253 P34972 Cannabinoid CB2 receptor 81.60% 97.25%
CHEMBL5805 Q9NR97 Toll-like receptor 8 80.85% 96.25%
CHEMBL2095172 P14867 GABA-A receptor; alpha-1/beta-2/gamma-2 80.22% 92.67%

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 72192561
LOTUS LTS0233471
wikiData Q77504792