Desotamide F

Details

Top
Internal ID 509da2c3-4b8a-4099-b3d2-f8994302dff8
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Amino acids, peptides, and analogues > Peptides > Oligopeptides
IUPAC Name 2-[(2S,8S,11S,14R,17S)-14-[(2S)-butan-2-yl]-17-[(2R)-butan-2-yl]-8-(1H-indol-3-ylmethyl)-11-(2-methylpropyl)-3,6,9,12,15,18-hexaoxo-1,4,7,10,13,16-hexazacyclooctadec-2-yl]acetamide
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C35H52N8O7/c1-7-19(5)29-34(49)41-26(15-27(36)44)31(46)38-17-28(45)39-25(14-21-16-37-23-12-10-9-11-22(21)23)32(47)40-24(13-18(3)4)33(48)42-30(20(6)8-2)35(50)43-29/h9-12,16,18-20,24-26,29-30,37H,7-8,13-15,17H2,1-6H3,(H2,36,44)(H,38,46)(H,39,45)(H,40,47)(H,41,49)(H,42,48)(H,43,50)/t19-,20+,24+,25+,26+,29+,30-/m1/s1
InChI Key YLZJYEWTPUAPEC-ARYILPDDSA-N
Popularity 2 references in papers

Physical and Chemical Properties

Top
Molecular Formula C35H52N8O7
Molecular Weight 696.80 g/mol
Exact Mass 696.39589603 g/mol
Topological Polar Surface Area (TPSA) 233.00 Ų
XlogP 2.20
Atomic LogP (AlogP) 0.28
H-Bond Acceptor 7
H-Bond Donor 8
Rotatable Bonds 10

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of Desotamide F

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9796 97.96%
Caco-2 - 0.8776 87.76%
Blood Brain Barrier - 0.5750 57.50%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Mitochondria 0.4107 41.07%
OATP2B1 inhibitior + 0.5559 55.59%
OATP1B1 inhibitior + 0.8889 88.89%
OATP1B3 inhibitior + 0.9366 93.66%
MATE1 inhibitior - 0.7858 78.58%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior + 0.9691 96.91%
P-glycoprotein inhibitior + 0.7848 78.48%
P-glycoprotein substrate + 0.8367 83.67%
CYP3A4 substrate + 0.6510 65.10%
CYP2C9 substrate - 0.7980 79.80%
CYP2D6 substrate - 0.8244 82.44%
CYP3A4 inhibition - 0.9237 92.37%
CYP2C9 inhibition - 0.8323 83.23%
CYP2C19 inhibition - 0.8421 84.21%
CYP2D6 inhibition - 0.9408 94.08%
CYP1A2 inhibition - 0.7872 78.72%
CYP2C8 inhibition - 0.5833 58.33%
CYP inhibitory promiscuity - 0.8744 87.44%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7900 79.00%
Carcinogenicity (trinary) Non-required 0.6563 65.63%
Eye corrosion - 0.9882 98.82%
Eye irritation - 0.9347 93.47%
Skin irritation - 0.7966 79.66%
Skin corrosion - 0.9343 93.43%
Ames mutagenesis - 0.7200 72.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3802 38.02%
Micronuclear + 0.7100 71.00%
Hepatotoxicity - 0.6341 63.41%
skin sensitisation - 0.8759 87.59%
Respiratory toxicity + 0.8000 80.00%
Reproductive toxicity + 0.8889 88.89%
Mitochondrial toxicity + 0.8250 82.50%
Nephrotoxicity - 0.6305 63.05%
Acute Oral Toxicity (c) III 0.5798 57.98%
Estrogen receptor binding + 0.7767 77.67%
Androgen receptor binding + 0.6552 65.52%
Thyroid receptor binding + 0.5879 58.79%
Glucocorticoid receptor binding + 0.6685 66.85%
Aromatase binding + 0.6335 63.35%
PPAR gamma + 0.7813 78.13%
Honey bee toxicity - 0.8137 81.37%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.7600 76.00%
Fish aquatic toxicity - 0.3791 37.91%

Targets

Top

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
CHEMBL4040 P28482 MAP kinase ERK2 99.58% 83.82%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 99.38% 91.11%
CHEMBL2581 P07339 Cathepsin D 98.64% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 98.42% 96.09%
CHEMBL3830 Q2M2I8 Adaptor-associated kinase 95.73% 83.10%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.64% 95.56%
CHEMBL3310 Q96DB2 Histone deacetylase 11 94.04% 88.56%
CHEMBL3137262 O60341 LSD1/CoREST complex 92.81% 97.09%
CHEMBL4071 P08311 Cathepsin G 92.14% 94.64%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 90.32% 94.45%
CHEMBL2693 Q9UIQ6 Cystinyl aminopeptidase 89.69% 97.64%
CHEMBL1937 Q92769 Histone deacetylase 2 89.63% 94.75%
CHEMBL5103 Q969S8 Histone deacetylase 10 89.43% 90.08%
CHEMBL255 P29275 Adenosine A2b receptor 89.08% 98.59%
CHEMBL2535 P11166 Glucose transporter 88.69% 98.75%
CHEMBL213 P08588 Beta-1 adrenergic receptor 87.59% 95.56%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 87.41% 92.62%
CHEMBL1806 P11388 DNA topoisomerase II alpha 87.09% 89.00%
CHEMBL253 P34972 Cannabinoid CB2 receptor 86.62% 97.25%
CHEMBL5896 O75164 Lysine-specific demethylase 4A 86.43% 99.09%
CHEMBL2443 P49862 Kallikrein 7 84.10% 94.00%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 83.54% 89.62%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 83.25% 96.47%
CHEMBL221 P23219 Cyclooxygenase-1 83.18% 90.17%
CHEMBL2996 Q05655 Protein kinase C delta 83.10% 97.79%
CHEMBL4208 P20618 Proteasome component C5 82.89% 90.00%
CHEMBL333 P08253 Matrix metalloproteinase-2 81.68% 96.31%
CHEMBL3155 P34969 Serotonin 7 (5-HT7) receptor 80.12% 90.71%

Plants that contains it

Top
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.
There are no matching plants.

Cross-Links

Top
PubChem 139588177
LOTUS LTS0255046
wikiData Q105350404