(1R,4S,10S,16S,19S)-4-[(2S)-butan-2-yl]-16-(2-methylbut-3-en-2-yloxymethyl)-19-(2-methylpropyl)-21-thia-3,6,12,15,18,23-hexazatricyclo[18.2.1.06,10]tricos-20(23)-ene-2,5,11,14,17-pentone

Details

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Internal ID ede80cb5-ea65-4edd-9b92-fe68ea9c8f5b
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Amino acids, peptides, and analogues > Peptides > Oligopeptides
IUPAC Name (1R,4S,10S,16S,19S)-4-[(2S)-butan-2-yl]-16-(2-methylbut-3-en-2-yloxymethyl)-19-(2-methylpropyl)-21-thia-3,6,12,15,18,23-hexazatricyclo[18.2.1.06,10]tricos-20(23)-ene-2,5,11,14,17-pentone
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C30H48N6O6S/c1-8-18(5)24-29(41)36-12-10-11-22(36)27(40)31-14-23(37)32-20(15-42-30(6,7)9-2)25(38)33-19(13-17(3)4)28-34-21(16-43-28)26(39)35-24/h9,17-22,24H,2,8,10-16H2,1,3-7H3,(H,31,40)(H,32,37)(H,33,38)(H,35,39)/t18-,19-,20-,21-,22-,24-/m0/s1
InChI Key FCGBWFPYRURNCX-KESUXUJOSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C30H48N6O6S
Molecular Weight 620.80 g/mol
Exact Mass 620.33560445 g/mol
Topological Polar Surface Area (TPSA) 184.00 Ų
XlogP 2.30
Atomic LogP (AlogP) 1.15
H-Bond Acceptor 8
H-Bond Donor 4
Rotatable Bonds 8

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (1R,4S,10S,16S,19S)-4-[(2S)-butan-2-yl]-16-(2-methylbut-3-en-2-yloxymethyl)-19-(2-methylpropyl)-21-thia-3,6,12,15,18,23-hexazatricyclo[18.2.1.06,10]tricos-20(23)-ene-2,5,11,14,17-pentone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8571 85.71%
Caco-2 - 0.8316 83.16%
Blood Brain Barrier - 0.6750 67.50%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Lysosomes 0.5227 52.27%
OATP2B1 inhibitior - 0.7161 71.61%
OATP1B1 inhibitior + 0.8419 84.19%
OATP1B3 inhibitior + 0.9316 93.16%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior + 0.9369 93.69%
P-glycoprotein inhibitior + 0.7474 74.74%
P-glycoprotein substrate + 0.7902 79.02%
CYP3A4 substrate + 0.6936 69.36%
CYP2C9 substrate - 0.8024 80.24%
CYP2D6 substrate - 0.8433 84.33%
CYP3A4 inhibition - 0.6976 69.76%
CYP2C9 inhibition - 0.8037 80.37%
CYP2C19 inhibition - 0.7416 74.16%
CYP2D6 inhibition - 0.8878 88.78%
CYP1A2 inhibition - 0.8413 84.13%
CYP2C8 inhibition + 0.5717 57.17%
CYP inhibitory promiscuity - 0.9364 93.64%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8200 82.00%
Carcinogenicity (trinary) Non-required 0.5457 54.57%
Eye corrosion - 0.9823 98.23%
Eye irritation - 0.9273 92.73%
Skin irritation - 0.7526 75.26%
Skin corrosion - 0.9004 90.04%
Ames mutagenesis - 0.5400 54.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5000 50.00%
Micronuclear + 0.7300 73.00%
Hepatotoxicity + 0.5462 54.62%
skin sensitisation - 0.8212 82.12%
Respiratory toxicity + 0.6889 68.89%
Reproductive toxicity + 0.8444 84.44%
Mitochondrial toxicity + 0.8125 81.25%
Nephrotoxicity + 0.4696 46.96%
Acute Oral Toxicity (c) III 0.5878 58.78%
Estrogen receptor binding + 0.7683 76.83%
Androgen receptor binding + 0.5945 59.45%
Thyroid receptor binding + 0.5604 56.04%
Glucocorticoid receptor binding + 0.6461 64.61%
Aromatase binding + 0.6843 68.43%
PPAR gamma + 0.6977 69.77%
Honey bee toxicity - 0.7038 70.38%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.6200 62.00%
Fish aquatic toxicity + 0.9489 94.89%

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 99.18% 97.25%
CHEMBL2581 P07339 Cathepsin D 99.00% 98.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 98.18% 94.45%
CHEMBL3524 P56524 Histone deacetylase 4 97.89% 92.97%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.53% 96.09%
CHEMBL5103 Q969S8 Histone deacetylase 10 96.52% 90.08%
CHEMBL1902 P62942 FK506-binding protein 1A 96.06% 97.05%
CHEMBL5203 P33316 dUTP pyrophosphatase 94.46% 99.18%
CHEMBL228 P31645 Serotonin transporter 93.59% 95.51%
CHEMBL2069156 Q14145 Kelch-like ECH-associated protein 1 92.87% 82.38%
CHEMBL3137262 O60341 LSD1/CoREST complex 92.01% 97.09%
CHEMBL4588 P22894 Matrix metalloproteinase 8 91.69% 94.66%
CHEMBL333 P08253 Matrix metalloproteinase-2 91.43% 96.31%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 90.96% 85.14%
CHEMBL2094135 Q96BI3 Gamma-secretase 89.76% 98.05%
CHEMBL2443 P49862 Kallikrein 7 89.71% 94.00%
CHEMBL5163 Q9NY46 Sodium channel protein type III alpha subunit 89.44% 96.90%
CHEMBL2693 Q9UIQ6 Cystinyl aminopeptidase 89.27% 97.64%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 88.83% 93.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 88.67% 95.89%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.81% 86.33%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 87.80% 89.34%
CHEMBL2073 P07947 Tyrosine-protein kinase YES 87.67% 83.14%
CHEMBL1937 Q92769 Histone deacetylase 2 87.37% 94.75%
CHEMBL221 P23219 Cyclooxygenase-1 87.23% 90.17%
CHEMBL5469 Q14289 Protein tyrosine kinase 2 beta 86.94% 91.03%
CHEMBL2781 P19634 Sodium/hydrogen exchanger 1 86.60% 90.24%
CHEMBL1907605 P24864 Cyclin-dependent kinase 2/cyclin E1 86.11% 92.88%
CHEMBL332 P03956 Matrix metalloproteinase-1 85.28% 94.50%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 85.12% 95.50%
CHEMBL4685 P14902 Indoleamine 2,3-dioxygenase 84.84% 96.38%
CHEMBL1795139 Q8IU80 Transmembrane protease serine 6 84.06% 98.33%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 83.69% 100.00%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 83.45% 93.40%
CHEMBL1801 P00747 Plasminogen 83.25% 92.44%
CHEMBL2189110 Q15910 Histone-lysine N-methyltransferase EZH2 83.16% 97.50%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 83.02% 97.14%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 82.76% 93.65%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 82.67% 91.11%
CHEMBL3691 Q13822 Autotaxin 82.57% 96.39%
CHEMBL1907601 P11802 Cyclin-dependent kinase 4/cyclin D1 82.15% 98.99%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 81.80% 95.56%
CHEMBL220 P22303 Acetylcholinesterase 80.90% 94.45%
CHEMBL4461 Q9NTG7 NAD-dependent deacetylase sirtuin 3 80.78% 94.36%
CHEMBL264 Q9Y5N1 Histamine H3 receptor 80.58% 91.43%
CHEMBL3310 Q96DB2 Histone deacetylase 11 80.58% 88.56%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 80.48% 96.47%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.39% 99.23%
CHEMBL4071 P08311 Cathepsin G 80.33% 94.64%

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 21585454
LOTUS LTS0174333
wikiData Q104993129