GameXPeptide A

Details

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Internal ID 294d3e79-eeeb-4a0f-9c2c-faa6f346b818
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Amino acids, peptides, and analogues > Peptides > Oligopeptides
IUPAC Name (3R,6S,9R,12S,15R)-3-benzyl-6,12,15-tris(2-methylpropyl)-9-propan-2-yl-1,4,7,10,13-pentazacyclopentadecane-2,5,8,11,14-pentone
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C32H51N5O5/c1-18(2)14-23-28(38)34-25(16-20(5)6)31(41)37-27(21(7)8)32(42)36-24(15-19(3)4)29(39)35-26(30(40)33-23)17-22-12-10-9-11-13-22/h9-13,18-21,23-27H,14-17H2,1-8H3,(H,33,40)(H,34,38)(H,35,39)(H,36,42)(H,37,41)/t23-,24+,25+,26-,27-/m1/s1
InChI Key GZKGGHUTCBGDES-LXSUACKSSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C32H51N5O5
Molecular Weight 585.80 g/mol
Exact Mass 585.38901974 g/mol
Topological Polar Surface Area (TPSA) 146.00 Ų
XlogP 5.30
Atomic LogP (AlogP) 2.46
H-Bond Acceptor 5
H-Bond Donor 5
Rotatable Bonds 9

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of GameXPeptide A

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9743 97.43%
Caco-2 - 0.7891 78.91%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability + 0.7429 74.29%
Subcellular localzation Mitochondria 0.6313 63.13%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9296 92.96%
OATP1B3 inhibitior + 0.9394 93.94%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9318 93.18%
BSEP inhibitior + 0.9381 93.81%
P-glycoprotein inhibitior + 0.7274 72.74%
P-glycoprotein substrate + 0.5408 54.08%
CYP3A4 substrate - 0.5675 56.75%
CYP2C9 substrate + 0.5733 57.33%
CYP2D6 substrate - 0.8372 83.72%
CYP3A4 inhibition - 0.8415 84.15%
CYP2C9 inhibition - 0.9361 93.61%
CYP2C19 inhibition - 0.7938 79.38%
CYP2D6 inhibition - 0.9473 94.73%
CYP1A2 inhibition - 0.9296 92.96%
CYP2C8 inhibition - 0.8785 87.85%
CYP inhibitory promiscuity - 0.9752 97.52%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7530 75.30%
Carcinogenicity (trinary) Non-required 0.7169 71.69%
Eye corrosion - 0.9882 98.82%
Eye irritation - 0.9456 94.56%
Skin irritation - 0.7858 78.58%
Skin corrosion - 0.9421 94.21%
Ames mutagenesis - 0.7100 71.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6665 66.65%
Micronuclear + 0.7400 74.00%
Hepatotoxicity + 0.6179 61.79%
skin sensitisation - 0.8740 87.40%
Respiratory toxicity + 0.7111 71.11%
Reproductive toxicity + 0.8111 81.11%
Mitochondrial toxicity + 0.6750 67.50%
Nephrotoxicity - 0.6348 63.48%
Acute Oral Toxicity (c) III 0.6308 63.08%
Estrogen receptor binding + 0.7339 73.39%
Androgen receptor binding + 0.5699 56.99%
Thyroid receptor binding + 0.5471 54.71%
Glucocorticoid receptor binding + 0.6806 68.06%
Aromatase binding + 0.6155 61.55%
PPAR gamma + 0.7060 70.60%
Honey bee toxicity - 0.9099 90.99%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.5100 51.00%
Fish aquatic toxicity - 0.3909 39.09%

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 99.21% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.22% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.92% 95.56%
CHEMBL4040 P28482 MAP kinase ERK2 92.24% 83.82%
CHEMBL221 P23219 Cyclooxygenase-1 89.17% 90.17%
CHEMBL2693 Q9UIQ6 Cystinyl aminopeptidase 88.06% 97.64%
CHEMBL5103 Q969S8 Histone deacetylase 10 85.58% 90.08%
CHEMBL1937 Q92769 Histone deacetylase 2 84.89% 94.75%
CHEMBL1949 P62937 Cyclophilin A 84.10% 98.57%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 82.83% 85.14%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 82.63% 91.11%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 82.48% 96.47%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 82.30% 94.45%
CHEMBL2563 Q9UQL6 Histone deacetylase 5 81.98% 89.67%
CHEMBL3401 O75469 Pregnane X receptor 81.83% 94.73%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 80.84% 95.50%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 80.66% 94.62%

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 101582538
LOTUS LTS0121383
wikiData Q77573481