Stylissamide F

Details

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Internal ID 0bcc7758-1ada-43fe-9126-dcd1eadca93b
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Amino acids, peptides, and analogues > Peptides > Oligopeptides
IUPAC Name 2-[(3S,9S,12S,15S,21S,24S,27S)-9,24-dibenzyl-12-[3-(diaminomethylideneamino)propyl]-2,8,11,14,20,23,26-heptaoxo-1,7,10,13,19,22,25-heptazatetracyclo[25.3.0.03,7.015,19]triacontan-21-yl]acetic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C43H56N10O9/c44-43(45)46-19-7-15-28-36(56)49-30(24-27-13-5-2-6-14-27)40(60)53-22-10-18-34(53)42(62)52-21-9-17-33(52)39(59)48-29(23-26-11-3-1-4-12-26)37(57)50-31(25-35(54)55)41(61)51-20-8-16-32(51)38(58)47-28/h1-6,11-14,28-34H,7-10,15-25H2,(H,47,58)(H,48,59)(H,49,56)(H,50,57)(H,54,55)(H4,44,45,46)/t28-,29-,30-,31-,32-,33-,34-/m0/s1
InChI Key AFISAWGAPBROEZ-NXBWRCJVSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C43H56N10O9
Molecular Weight 857.00 g/mol
Exact Mass 856.42317340 g/mol
Topological Polar Surface Area (TPSA) 279.00 Ų
XlogP 0.30
Atomic LogP (AlogP) -1.07
H-Bond Acceptor 9
H-Bond Donor 7
Rotatable Bonds 10

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Stylissamide F

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.6450 64.50%
Caco-2 - 0.8830 88.30%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Mitochondria 0.6170 61.70%
OATP2B1 inhibitior + 0.5564 55.64%
OATP1B1 inhibitior + 0.8866 88.66%
OATP1B3 inhibitior + 0.9404 94.04%
MATE1 inhibitior - 0.5600 56.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior + 0.9059 90.59%
P-glycoprotein inhibitior + 0.7610 76.10%
P-glycoprotein substrate + 0.7615 76.15%
CYP3A4 substrate + 0.6131 61.31%
CYP2C9 substrate - 0.8210 82.10%
CYP2D6 substrate - 0.7762 77.62%
CYP3A4 inhibition - 0.9630 96.30%
CYP2C9 inhibition - 0.9238 92.38%
CYP2C19 inhibition - 0.8969 89.69%
CYP2D6 inhibition - 0.9268 92.68%
CYP1A2 inhibition - 0.9042 90.42%
CYP2C8 inhibition + 0.5101 51.01%
CYP inhibitory promiscuity - 0.9940 99.40%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8900 89.00%
Carcinogenicity (trinary) Non-required 0.6315 63.15%
Eye corrosion - 0.9900 99.00%
Eye irritation - 0.9166 91.66%
Skin irritation - 0.7608 76.08%
Skin corrosion - 0.9372 93.72%
Ames mutagenesis - 0.6600 66.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4795 47.95%
Micronuclear + 0.9100 91.00%
Hepatotoxicity + 0.5608 56.08%
skin sensitisation - 0.8626 86.26%
Respiratory toxicity + 0.9111 91.11%
Reproductive toxicity + 0.9333 93.33%
Mitochondrial toxicity + 0.9000 90.00%
Nephrotoxicity + 0.4655 46.55%
Acute Oral Toxicity (c) III 0.5670 56.70%
Estrogen receptor binding + 0.7882 78.82%
Androgen receptor binding + 0.6647 66.47%
Thyroid receptor binding + 0.5854 58.54%
Glucocorticoid receptor binding + 0.5717 57.17%
Aromatase binding + 0.5799 57.99%
PPAR gamma + 0.7431 74.31%
Honey bee toxicity - 0.9208 92.08%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.5800 58.00%
Fish aquatic toxicity + 0.7585 75.85%

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 99.26% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 98.95% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.09% 91.11%
CHEMBL2693 Q9UIQ6 Cystinyl aminopeptidase 95.47% 97.64%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.64% 95.56%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 93.90% 94.45%
CHEMBL1902 P62942 FK506-binding protein 1A 93.38% 97.05%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 92.50% 93.03%
CHEMBL5608 Q16288 NT-3 growth factor receptor 92.00% 95.89%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 91.22% 93.00%
CHEMBL2069156 Q14145 Kelch-like ECH-associated protein 1 90.62% 82.38%
CHEMBL3137262 O60341 LSD1/CoREST complex 89.84% 97.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.45% 86.33%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 83.55% 85.14%
CHEMBL4071 P08311 Cathepsin G 83.43% 94.64%
CHEMBL217 P14416 Dopamine D2 receptor 83.08% 95.62%
CHEMBL4447 Q9Y337 Kallikrein 5 80.09% 87.50%

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 46210325
LOTUS LTS0226923
wikiData Q104911252