For-DL-Met-DL-Asn-DL-Val-DL-xiIle-DL-xiThr-DL-Asn-DL-Leu-DL-Leu-DL-Ala-Gly-DL-Val-DL-Val-DL-His-DL-Phe-DL-Leu-Gly-DL-Trp-DL-Leu-DL-Val-OH

Details

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Internal ID 746977ae-ffb8-45e0-8881-e92543508fdc
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Amino acids, peptides, and analogues > Peptides
IUPAC Name 2-[[2-[[2-[[2-[[2-[[2-[[2-[[2-[[2-[[2-[2-[[2-[[2-[[4-amino-2-[[2-[[2-[[2-[[4-amino-2-[(2-formamido-4-methylsulfanylbutanoyl)amino]-4-oxobutanoyl]amino]-3-methylbutanoyl]amino]-3-methylpentanoyl]amino]-3-hydroxybutanoyl]amino]-4-oxobutanoyl]amino]-4-methylpentanoyl]amino]-4-methylpentanoyl]amino]propanoylamino]acetyl]amino]-3-methylbutanoyl]amino]-3-methylbutanoyl]amino]-3-(1H-imidazol-5-yl)propanoyl]amino]-3-phenylpropanoyl]amino]-4-methylpentanoyl]amino]acetyl]amino]-3-(1H-indol-3-yl)propanoyl]amino]-4-methylpentanoyl]amino]-3-methylbutanoic acid
SMILES (Canonical) CCC(C)C(C(=O)NC(C(C)O)C(=O)NC(CC(=O)N)C(=O)NC(CC(C)C)C(=O)NC(CC(C)C)C(=O)NC(C)C(=O)NCC(=O)NC(C(C)C)C(=O)NC(C(C)C)C(=O)NC(CC1=CN=CN1)C(=O)NC(CC2=CC=CC=C2)C(=O)NC(CC(C)C)C(=O)NCC(=O)NC(CC3=CNC4=CC=CC=C43)C(=O)NC(CC(C)C)C(=O)NC(C(C)C)C(=O)O)NC(=O)C(C(C)C)NC(=O)C(CC(=O)N)NC(=O)C(CCSC)NC=O
SMILES (Isomeric) CCC(C)C(C(=O)NC(C(C)O)C(=O)NC(CC(=O)N)C(=O)NC(CC(C)C)C(=O)NC(CC(C)C)C(=O)NC(C)C(=O)NCC(=O)NC(C(C)C)C(=O)NC(C(C)C)C(=O)NC(CC1=CN=CN1)C(=O)NC(CC2=CC=CC=C2)C(=O)NC(CC(C)C)C(=O)NCC(=O)NC(CC3=CNC4=CC=CC=C43)C(=O)NC(CC(C)C)C(=O)NC(C(C)C)C(=O)O)NC(=O)C(C(C)C)NC(=O)C(CC(=O)N)NC(=O)C(CCSC)NC=O
InChI InChI=1S/C101H158N24O24S/c1-22-57(18)83(124-98(145)81(55(14)15)121-95(142)74(42-76(103)129)117-87(134)65(109-48-126)32-33-150-21)99(146)125-84(59(20)127)100(147)119-73(41-75(102)128)93(140)114-68(36-51(6)7)89(136)113-67(35-50(4)5)88(135)110-58(19)85(132)106-46-78(131)120-79(53(10)11)97(144)122-80(54(12)13)96(143)118-72(40-62-44-104-47-108-62)92(139)116-70(38-60-28-24-23-25-29-60)90(137)112-66(34-49(2)3)86(133)107-45-77(130)111-71(39-61-43-105-64-31-27-26-30-63(61)64)91(138)115-69(37-52(8)9)94(141)123-82(56(16)17)101(148)149/h23-31,43-44,47-59,65-74,79-84,105,127H,22,32-42,45-46H2,1-21H3,(H2,102,128)(H2,103,129)(H,104,108)(H,106,132)(H,107,133)(H,109,126)(H,110,135)(H,111,130)(H,112,137)(H,113,136)(H,114,140)(H,115,138)(H,116,139)(H,117,134)(H,118,143)(H,119,147)(H,120,131)(H,121,142)(H,122,144)(H,123,141)(H,124,145)(H,125,146)(H,148,149)
InChI Key ZHTFBHZIAUJLCN-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C101H158N24O24S
Molecular Weight 2124.50 g/mol
Exact Mass 2124.16350801 g/mol
Topological Polar Surface Area (TPSA) 766.00 Ų
XlogP 4.70
Atomic LogP (AlogP) -2.13
H-Bond Acceptor 25
H-Bond Donor 25
Rotatable Bonds 67

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of For-DL-Met-DL-Asn-DL-Val-DL-xiIle-DL-xiThr-DL-Asn-DL-Leu-DL-Leu-DL-Ala-Gly-DL-Val-DL-Val-DL-His-DL-Phe-DL-Leu-Gly-DL-Trp-DL-Leu-DL-Val-OH

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9201 92.01%
Caco-2 - 0.8646 86.46%
Blood Brain Barrier - 0.6500 65.00%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Mitochondria 0.3578 35.78%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.7645 76.45%
OATP1B3 inhibitior + 0.9332 93.32%
MATE1 inhibitior - 0.8409 84.09%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior + 0.9664 96.64%
P-glycoprotein inhibitior + 0.7418 74.18%
P-glycoprotein substrate + 0.8766 87.66%
CYP3A4 substrate + 0.7379 73.79%
CYP2C9 substrate - 0.5983 59.83%
CYP2D6 substrate - 0.8533 85.33%
CYP3A4 inhibition - 0.7034 70.34%
CYP2C9 inhibition - 0.7204 72.04%
CYP2C19 inhibition - 0.7636 76.36%
CYP2D6 inhibition - 0.8863 88.63%
CYP1A2 inhibition - 0.8474 84.74%
CYP2C8 inhibition + 0.8174 81.74%
CYP inhibitory promiscuity - 0.8880 88.80%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.8800 88.00%
Carcinogenicity (trinary) Non-required 0.6283 62.83%
Eye corrosion - 0.9874 98.74%
Eye irritation - 0.8954 89.54%
Skin irritation - 0.7901 79.01%
Skin corrosion - 0.9279 92.79%
Ames mutagenesis - 0.7800 78.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7047 70.47%
Micronuclear + 0.6400 64.00%
Hepatotoxicity + 0.5500 55.00%
skin sensitisation - 0.8669 86.69%
Respiratory toxicity + 0.8222 82.22%
Reproductive toxicity + 0.9444 94.44%
Mitochondrial toxicity + 0.8750 87.50%
Nephrotoxicity - 0.7834 78.34%
Acute Oral Toxicity (c) III 0.5544 55.44%
Estrogen receptor binding - 0.5211 52.11%
Androgen receptor binding + 0.7318 73.18%
Thyroid receptor binding + 0.7948 79.48%
Glucocorticoid receptor binding + 0.8405 84.05%
Aromatase binding + 0.8038 80.38%
PPAR gamma + 0.7578 75.78%
Honey bee toxicity - 0.6550 65.50%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.7200 72.00%
Fish aquatic toxicity - 0.3870 38.70%

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 99.97% 98.95%
CHEMBL230 P35354 Cyclooxygenase-2 99.82% 89.63%
CHEMBL1255126 O15151 Protein Mdm4 99.56% 90.20%
CHEMBL1907594 P30926 Neuronal acetylcholine receptor; alpha3/beta4 98.93% 97.23%
CHEMBL221 P23219 Cyclooxygenase-1 98.91% 90.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 98.34% 96.09%
CHEMBL2693 Q9UIQ6 Cystinyl aminopeptidase 97.21% 97.64%
CHEMBL2492 P36544 Neuronal acetylcholine receptor protein alpha-7 subunit 96.85% 88.42%
CHEMBL4040 P28482 MAP kinase ERK2 96.74% 83.82%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.32% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.79% 95.56%
CHEMBL1795139 Q8IU80 Transmembrane protease serine 6 94.63% 98.33%
CHEMBL2535 P11166 Glucose transporter 94.50% 98.75%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 94.29% 100.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 94.18% 99.17%
CHEMBL3837 P07711 Cathepsin L 93.68% 96.61%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 93.27% 96.00%
CHEMBL5939 Q9NZ08 Endoplasmic reticulum aminopeptidase 1 93.04% 100.00%
CHEMBL3176 O43603 Galanin receptor 2 92.86% 98.89%
CHEMBL2095164 P49354 Geranylgeranyl transferase type I 92.47% 92.80%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 91.40% 95.50%
CHEMBL2514 O95665 Neurotensin receptor 2 90.59% 100.00%
CHEMBL3359 P21462 Formyl peptide receptor 1 90.52% 93.56%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 90.43% 91.81%
CHEMBL5163 Q9NY46 Sodium channel protein type III alpha subunit 89.96% 96.90%
CHEMBL2179 P04062 Beta-glucocerebrosidase 88.90% 85.31%
CHEMBL4018 P49146 Neuropeptide Y receptor type 2 88.30% 98.94%
CHEMBL4801 P29466 Caspase-1 87.03% 96.85%
CHEMBL2094135 Q96BI3 Gamma-secretase 86.90% 98.05%
CHEMBL3392948 Q9NP59 Solute carrier family 40 member 1 86.52% 95.00%
CHEMBL1287628 Q9Y5S8 NADPH oxidase 1 85.21% 95.48%
CHEMBL3310 Q96DB2 Histone deacetylase 11 84.98% 88.56%
CHEMBL2885 P07451 Carbonic anhydrase III 84.21% 87.45%
CHEMBL213 P08588 Beta-1 adrenergic receptor 84.06% 95.56%
CHEMBL2413 P32246 C-C chemokine receptor type 1 83.39% 89.50%
CHEMBL259 P32245 Melanocortin receptor 4 82.80% 95.38%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 82.43% 94.45%
CHEMBL5028 O14672 ADAM10 82.16% 97.50%
CHEMBL3976 Q9UHL4 Dipeptidyl peptidase II 81.70% 92.29%
CHEMBL4361 Q07820 Induced myeloid leukemia cell differentiation protein Mcl-1 81.56% 95.52%
CHEMBL3663 P62993 Growth factor receptor-bound protein 2 81.50% 90.00%
CHEMBL1781 P11387 DNA topoisomerase I 81.13% 97.00%

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 162821009
LOTUS LTS0166034
wikiData Q105375993