Ac-Aib-Asn-Ile-Ile-Aib-Pro-Leu-Leu-Aib-Pro-Leu-ol

Details

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Internal ID 23978de4-5924-4394-8f01-d1c1260ccbf0
Taxonomy Organic Polymers > Polypeptides
IUPAC Name (2S)-2-[(2-acetamido-2-methylpropanoyl)amino]-N-[(2S,3S)-1-[[(2S,3S)-1-[[1-[(2S)-2-[[(2S)-1-[[(2S)-1-[[1-[(2S)-2-[[(2S)-1-hydroxy-4-methylpentan-2-yl]carbamoyl]pyrrolidin-1-yl]-2-methyl-1-oxopropan-2-yl]amino]-4-methyl-1-oxopentan-2-yl]amino]-4-methyl-1-oxopentan-2-yl]carbamoyl]pyrrolidin-1-yl]-2-methyl-1-oxopropan-2-yl]amino]-3-methyl-1-oxopentan-2-yl]amino]-3-methyl-1-oxopentan-2-yl]butanediamide
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C58H102N12O13/c1-18-34(9)44(64-47(75)40(29-43(59)73)63-53(81)56(12,13)66-36(11)72)51(79)65-45(35(10)19-2)52(80)68-58(16,17)55(83)70-25-21-23-42(70)50(78)62-38(27-32(5)6)46(74)61-39(28-33(7)8)48(76)67-57(14,15)54(82)69-24-20-22-41(69)49(77)60-37(30-71)26-31(3)4/h31-35,37-42,44-45,71H,18-30H2,1-17H3,(H2,59,73)(H,60,77)(H,61,74)(H,62,78)(H,63,81)(H,64,75)(H,65,79)(H,66,72)(H,67,76)(H,68,80)/t34-,35-,37-,38-,39-,40-,41-,42-,44-,45-/m0/s1
InChI Key SUJVHTVAUFPDNS-LRYCKQPWSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C58H102N12O13
Molecular Weight 1175.50 g/mol
Exact Mass 1174.76893135 g/mol
Topological Polar Surface Area (TPSA) 366.00 Ų
XlogP 3.00
Atomic LogP (AlogP) 0.68
H-Bond Acceptor 13
H-Bond Donor 11
Rotatable Bonds 32

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Ac-Aib-Asn-Ile-Ile-Aib-Pro-Leu-Leu-Aib-Pro-Leu-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.6307 63.07%
Caco-2 - 0.8600 86.00%
Blood Brain Barrier - 0.6750 67.50%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Lysosomes 0.6705 67.05%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8697 86.97%
OATP1B3 inhibitior + 0.9339 93.39%
MATE1 inhibitior - 0.9412 94.12%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior + 0.9247 92.47%
P-glycoprotein inhibitior + 0.7428 74.28%
P-glycoprotein substrate + 0.8616 86.16%
CYP3A4 substrate + 0.7062 70.62%
CYP2C9 substrate - 0.7929 79.29%
CYP2D6 substrate - 0.8494 84.94%
CYP3A4 inhibition - 0.6870 68.70%
CYP2C9 inhibition - 0.8665 86.65%
CYP2C19 inhibition - 0.7879 78.79%
CYP2D6 inhibition - 0.8833 88.33%
CYP1A2 inhibition - 0.8821 88.21%
CYP2C8 inhibition + 0.4804 48.04%
CYP inhibitory promiscuity - 0.9641 96.41%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.7400 74.00%
Carcinogenicity (trinary) Non-required 0.6227 62.27%
Eye corrosion - 0.9802 98.02%
Eye irritation - 0.8966 89.66%
Skin irritation - 0.7762 77.62%
Skin corrosion - 0.8955 89.55%
Ames mutagenesis - 0.6500 65.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3952 39.52%
Micronuclear + 0.6600 66.00%
Hepatotoxicity + 0.6407 64.07%
skin sensitisation - 0.8557 85.57%
Respiratory toxicity + 0.7222 72.22%
Reproductive toxicity + 0.8222 82.22%
Mitochondrial toxicity + 0.7000 70.00%
Nephrotoxicity + 0.5411 54.11%
Acute Oral Toxicity (c) III 0.6368 63.68%
Estrogen receptor binding + 0.6888 68.88%
Androgen receptor binding + 0.7515 75.15%
Thyroid receptor binding + 0.5884 58.84%
Glucocorticoid receptor binding + 0.6842 68.42%
Aromatase binding + 0.7173 71.73%
PPAR gamma + 0.7771 77.71%
Honey bee toxicity - 0.8392 83.92%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.6800 68.00%
Fish aquatic toxicity - 0.6671 66.71%

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
CHEMBL3837 P07711 Cathepsin L 99.76% 96.61%
CHEMBL2581 P07339 Cathepsin D 99.60% 98.95%
CHEMBL253 P34972 Cannabinoid CB2 receptor 98.80% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 98.58% 96.09%
CHEMBL4018 P49146 Neuropeptide Y receptor type 2 98.55% 98.94%
CHEMBL3024 P53350 Serine/threonine-protein kinase PLK1 98.36% 97.43%
CHEMBL4123 P30989 Neurotensin receptor 1 98.28% 96.67%
CHEMBL1795139 Q8IU80 Transmembrane protease serine 6 98.12% 98.33%
CHEMBL4801 P29466 Caspase-1 97.51% 96.85%
CHEMBL3359 P21462 Formyl peptide receptor 1 97.26% 93.56%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 96.93% 96.95%
CHEMBL2514 O95665 Neurotensin receptor 2 96.55% 100.00%
CHEMBL2730 P21980 Protein-glutamine gamma-glutamyltransferase 95.81% 92.38%
CHEMBL237 P41145 Kappa opioid receptor 95.33% 98.10%
CHEMBL340 P08684 Cytochrome P450 3A4 95.04% 91.19%
CHEMBL3468 P55210 Caspase-7 94.98% 95.68%
CHEMBL4625 Q07817 Apoptosis regulator Bcl-X 94.83% 99.77%
CHEMBL4588 P22894 Matrix metalloproteinase 8 94.77% 94.66%
CHEMBL333 P08253 Matrix metalloproteinase-2 94.65% 96.31%
CHEMBL3437 Q16853 Amine oxidase, copper containing 94.49% 94.00%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 94.03% 97.21%
CHEMBL4394 Q9NYA1 Sphingosine kinase 1 93.99% 96.03%
CHEMBL1944495 P28065 Proteasome subunit beta type-9 93.95% 97.50%
CHEMBL2693 Q9UIQ6 Cystinyl aminopeptidase 93.51% 97.64%
CHEMBL4227 P25090 Lipoxin A4 receptor 93.37% 100.00%
CHEMBL3176 O43603 Galanin receptor 2 93.27% 98.89%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 93.21% 97.14%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 93.08% 100.00%
CHEMBL259 P32245 Melanocortin receptor 4 92.93% 95.38%
CHEMBL321 P14780 Matrix metalloproteinase 9 92.74% 92.12%
CHEMBL4777 P25929 Neuropeptide Y receptor type 1 92.53% 96.67%
CHEMBL3137262 O60341 LSD1/CoREST complex 91.33% 97.09%
CHEMBL4461 Q9NTG7 NAD-dependent deacetylase sirtuin 3 91.23% 94.36%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 90.91% 96.47%
CHEMBL4361 Q07820 Induced myeloid leukemia cell differentiation protein Mcl-1 90.36% 95.52%
CHEMBL4005 P42336 PI3-kinase p110-alpha subunit 89.95% 97.47%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 88.20% 94.33%
CHEMBL4979 P13866 Sodium/glucose cotransporter 1 88.11% 98.24%
CHEMBL2492 P36544 Neuronal acetylcholine receptor protein alpha-7 subunit 87.20% 88.42%
CHEMBL2073 P07947 Tyrosine-protein kinase YES 87.20% 83.14%
CHEMBL5608 Q16288 NT-3 growth factor receptor 86.61% 95.89%
CHEMBL2095194 P08709 Coagulation factor VII/tissue factor 86.38% 99.17%
CHEMBL2094135 Q96BI3 Gamma-secretase 86.24% 98.05%
CHEMBL3830 Q2M2I8 Adaptor-associated kinase 86.08% 83.10%
CHEMBL2664 P23526 Adenosylhomocysteinase 85.62% 86.67%
CHEMBL5966 P55899 IgG receptor FcRn large subunit p51 85.26% 90.93%
CHEMBL1907594 P30926 Neuronal acetylcholine receptor; alpha3/beta4 85.11% 97.23%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 84.41% 96.21%
CHEMBL5163 Q9NY46 Sodium channel protein type III alpha subunit 84.09% 96.90%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 83.90% 90.71%
CHEMBL3145 P42338 PI3-kinase p110-beta subunit 83.64% 98.75%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 83.09% 100.00%
CHEMBL2413 P32246 C-C chemokine receptor type 1 83.05% 89.50%
CHEMBL4015 P41597 C-C chemokine receptor type 2 82.84% 98.57%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 82.82% 93.00%
CHEMBL5028 O14672 ADAM10 82.76% 97.50%
CHEMBL236 P41143 Delta opioid receptor 82.58% 99.35%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 82.55% 95.50%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.26% 99.17%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 81.92% 91.81%
CHEMBL3691 Q13822 Autotaxin 81.68% 96.39%
CHEMBL4816 Q9Y243 Serine/threonine-protein kinase AKT3 81.56% 96.28%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 81.48% 93.04%
CHEMBL3392948 Q9NP59 Solute carrier family 40 member 1 81.47% 95.00%
CHEMBL3267 P48736 PI3-kinase p110-gamma subunit 81.32% 95.71%
CHEMBL255 P29275 Adenosine A2b receptor 81.16% 98.59%
CHEMBL5285 Q99683 Mitogen-activated protein kinase kinase kinase 5 81.09% 92.26%
CHEMBL3430907 Q96GD4 Aurora kinase B/Inner centromere protein 81.05% 97.50%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 80.42% 95.89%
CHEMBL4660 P28907 Lymphocyte differentiation antigen CD38 80.21% 95.27%
CHEMBL5203 P33316 dUTP pyrophosphatase 80.08% 99.18%
CHEMBL1873 P00750 Tissue-type plasminogen activator 80.02% 93.33%

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 10534341
LOTUS LTS0061867
wikiData Q105261005