cyclo[Ala-Asp(Ph(2-NH2))-D-aThr-Pro-Gly-DL-aIle-Asn]

Details

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Internal ID 97b6d19f-3aac-4804-a2f5-32fcf4987ec1
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Amino acids, peptides, and analogues > Peptides > Oligopeptides
IUPAC Name 2-[(3R,6S,9S,12S,21S)-6-[2-(2-aminophenyl)-2-oxoethyl]-15-[(2R)-butan-2-yl]-3-[(1R)-1-hydroxyethyl]-9-methyl-2,5,8,11,14,17,20-heptaoxo-1,4,7,10,13,16,19-heptazabicyclo[19.3.0]tetracosan-12-yl]acetamide
SMILES (Canonical) CCC(C)C1C(=O)NC(C(=O)NC(C(=O)NC(C(=O)NC(C(=O)N2CCCC2C(=O)NCC(=O)N1)C(C)O)CC(=O)C3=CC=CC=C3N)C)CC(=O)N
SMILES (Isomeric) CC[C@@H](C)C1C(=O)N[C@H](C(=O)N[C@H](C(=O)N[C@H](C(=O)N[C@@H](C(=O)N2CCC[C@H]2C(=O)NCC(=O)N1)[C@@H](C)O)CC(=O)C3=CC=CC=C3N)C)CC(=O)N
InChI InChI=1S/C34H49N9O10/c1-5-16(2)27-33(52)40-22(14-25(36)46)30(49)38-17(3)29(48)39-21(13-24(45)19-9-6-7-10-20(19)35)31(50)42-28(18(4)44)34(53)43-12-8-11-23(43)32(51)37-15-26(47)41-27/h6-7,9-10,16-18,21-23,27-28,44H,5,8,11-15,35H2,1-4H3,(H2,36,46)(H,37,51)(H,38,49)(H,39,48)(H,40,52)(H,41,47)(H,42,50)/t16-,17+,18-,21+,22+,23+,27?,28-/m1/s1
InChI Key XYTBGJYRMURKBQ-TZKIHJEDSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C34H49N9O10
Molecular Weight 743.80 g/mol
Exact Mass 743.36023879 g/mol
Topological Polar Surface Area (TPSA) 301.00 Ų
XlogP -1.30
Atomic LogP (AlogP) -3.29
H-Bond Acceptor 11
H-Bond Donor 9
Rotatable Bonds 8

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of cyclo[Ala-Asp(Ph(2-NH2))-D-aThr-Pro-Gly-DL-aIle-Asn]

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.7747 77.47%
Caco-2 - 0.8855 88.55%
Blood Brain Barrier - 0.7250 72.50%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Mitochondria 0.4462 44.62%
OATP2B1 inhibitior + 0.5529 55.29%
OATP1B1 inhibitior + 0.8408 84.08%
OATP1B3 inhibitior + 0.9331 93.31%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior + 0.7242 72.42%
P-glycoprotein inhibitior + 0.7523 75.23%
P-glycoprotein substrate + 0.8686 86.86%
CYP3A4 substrate + 0.6660 66.60%
CYP2C9 substrate + 0.6064 60.64%
CYP2D6 substrate - 0.8146 81.46%
CYP3A4 inhibition - 0.9630 96.30%
CYP2C9 inhibition - 0.9324 93.24%
CYP2C19 inhibition - 0.9267 92.67%
CYP2D6 inhibition - 0.9156 91.56%
CYP1A2 inhibition - 0.9399 93.99%
CYP2C8 inhibition + 0.5614 56.14%
CYP inhibitory promiscuity - 0.9847 98.47%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.8400 84.00%
Carcinogenicity (trinary) Non-required 0.6468 64.68%
Eye corrosion - 0.9892 98.92%
Eye irritation - 0.9245 92.45%
Skin irritation - 0.7856 78.56%
Skin corrosion - 0.9340 93.40%
Ames mutagenesis - 0.7654 76.54%
Human Ether-a-go-go-Related Gene inhibition - 0.3951 39.51%
Micronuclear + 0.9300 93.00%
Hepatotoxicity + 0.5355 53.55%
skin sensitisation - 0.8826 88.26%
Respiratory toxicity + 0.8222 82.22%
Reproductive toxicity + 0.9444 94.44%
Mitochondrial toxicity + 0.9000 90.00%
Nephrotoxicity + 0.5678 56.78%
Acute Oral Toxicity (c) III 0.5845 58.45%
Estrogen receptor binding + 0.7600 76.00%
Androgen receptor binding + 0.5672 56.72%
Thyroid receptor binding + 0.5549 55.49%
Glucocorticoid receptor binding + 0.5956 59.56%
Aromatase binding + 0.6318 63.18%
PPAR gamma + 0.7632 76.32%
Honey bee toxicity - 0.8021 80.21%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.8100 81.00%
Fish aquatic toxicity + 0.6462 64.62%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 99.40% 96.09%
CHEMBL2581 P07339 Cathepsin D 99.28% 98.95%
CHEMBL253 P34972 Cannabinoid CB2 receptor 96.86% 97.25%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 95.90% 85.14%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.66% 91.11%
CHEMBL2443 P49862 Kallikrein 7 94.50% 94.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 93.36% 97.09%
CHEMBL4071 P08311 Cathepsin G 93.01% 94.64%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.66% 95.56%
CHEMBL5608 Q16288 NT-3 growth factor receptor 91.45% 95.89%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 91.27% 93.00%
CHEMBL221 P23219 Cyclooxygenase-1 88.57% 90.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.88% 86.33%
CHEMBL4208 P20618 Proteasome component C5 86.56% 90.00%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 86.11% 93.03%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 85.28% 97.14%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 85.10% 90.71%
CHEMBL2069156 Q14145 Kelch-like ECH-associated protein 1 83.11% 82.38%
CHEMBL228 P31645 Serotonin transporter 81.91% 95.51%

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 163190260
LOTUS LTS0005139
wikiData Q105344650