Grassypeptolide F

Details

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Internal ID 1849d0f1-c45e-48d0-8c40-450edda002f2
Taxonomy Organic acids and derivatives > Peptidomimetics > Depsipeptides > Cyclic depsipeptides
IUPAC Name (2R,5R,9R,12S,18S,21S,24R,25R,28R,31R,34R)-9,21,31-tribenzyl-2-ethyl-10,19,24,25,32-pentamethyl-18,28-di(propan-2-yl)-22-oxa-7,36-dithia-3,10,16,19,26,29,32,37,38-nonazatetracyclo[32.2.1.15,8.012,16]octatriaconta-1(37),8(38)-diene-4,11,17,20,23,27,30,33-octone
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C60H79N9O9S2/c1-11-42-54-64-44(34-79-54)56(73)66(8)46(30-39-22-15-12-16-23-39)52(71)65-49(35(2)3)53(72)61-38(7)37(6)60(77)78-48(32-41-26-19-14-20-27-41)58(75)68(10)50(36(4)5)59(76)69-29-21-28-45(69)57(74)67(9)47(31-40-24-17-13-18-25-40)55-63-43(33-80-55)51(70)62-42/h12-20,22-27,35-38,42-50H,11,21,28-34H2,1-10H3,(H,61,72)(H,62,70)(H,65,71)/t37-,38-,42-,43+,44+,45+,46-,47-,48+,49-,50+/m1/s1
InChI Key OMAHHNNQYKBGML-REKYTSBZSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C60H79N9O9S2
Molecular Weight 1134.50 g/mol
Exact Mass 1133.54421748 g/mol
Topological Polar Surface Area (TPSA) 270.00 Ų
XlogP 7.80
Atomic LogP (AlogP) 4.97
H-Bond Acceptor 13
H-Bond Donor 3
Rotatable Bonds 9

Synonyms

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CHEMBL1823866
CHEBI:69193
Grassypeptolides F
DTXSID001046409
BDBM50352478
Q27137532

2D Structure

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2D Structure of Grassypeptolide F

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.6622 66.22%
Caco-2 - 0.8623 86.23%
Blood Brain Barrier - 0.9250 92.50%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Lysosomes 0.5177 51.77%
OATP2B1 inhibitior - 0.8539 85.39%
OATP1B1 inhibitior + 0.8368 83.68%
OATP1B3 inhibitior + 0.9233 92.33%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior + 0.9522 95.22%
P-glycoprotein inhibitior + 0.7513 75.13%
P-glycoprotein substrate + 0.8361 83.61%
CYP3A4 substrate + 0.7103 71.03%
CYP2C9 substrate - 0.5814 58.14%
CYP2D6 substrate - 0.8149 81.49%
CYP3A4 inhibition - 0.6002 60.02%
CYP2C9 inhibition - 0.6727 67.27%
CYP2C19 inhibition - 0.6019 60.19%
CYP2D6 inhibition - 0.8385 83.85%
CYP1A2 inhibition - 0.8474 84.74%
CYP2C8 inhibition + 0.6649 66.49%
CYP inhibitory promiscuity - 0.8833 88.33%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8400 84.00%
Carcinogenicity (trinary) Non-required 0.6161 61.61%
Eye corrosion - 0.9873 98.73%
Eye irritation - 0.9007 90.07%
Skin irritation - 0.7724 77.24%
Skin corrosion - 0.9208 92.08%
Ames mutagenesis - 0.5800 58.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7338 73.38%
Micronuclear + 0.7500 75.00%
Hepatotoxicity + 0.6517 65.17%
skin sensitisation - 0.8467 84.67%
Respiratory toxicity + 0.8444 84.44%
Reproductive toxicity + 0.9333 93.33%
Mitochondrial toxicity + 0.8750 87.50%
Nephrotoxicity - 0.8967 89.67%
Acute Oral Toxicity (c) III 0.6249 62.49%
Estrogen receptor binding + 0.7807 78.07%
Androgen receptor binding + 0.7468 74.68%
Thyroid receptor binding + 0.6832 68.32%
Glucocorticoid receptor binding + 0.7630 76.30%
Aromatase binding + 0.6357 63.57%
PPAR gamma + 0.8055 80.55%
Honey bee toxicity - 0.7697 76.97%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity - 0.5800 58.00%
Fish aquatic toxicity + 0.9769 97.69%

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 99.54% 98.95%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 98.14% 85.14%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 98.12% 94.45%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.36% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 97.13% 97.25%
CHEMBL5103 Q969S8 Histone deacetylase 10 96.03% 90.08%
CHEMBL2693 Q9UIQ6 Cystinyl aminopeptidase 95.70% 97.64%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.32% 95.56%
CHEMBL1902 P62942 FK506-binding protein 1A 93.35% 97.05%
CHEMBL1978 P11511 Cytochrome P450 19A1 92.35% 91.76%
CHEMBL333 P08253 Matrix metalloproteinase-2 92.24% 96.31%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.34% 86.33%
CHEMBL5608 Q16288 NT-3 growth factor receptor 91.04% 95.89%
CHEMBL2069156 Q14145 Kelch-like ECH-associated protein 1 90.86% 82.38%
CHEMBL3137262 O60341 LSD1/CoREST complex 89.65% 97.09%
CHEMBL1949 P62937 Cyclophilin A 88.71% 98.57%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 87.15% 99.23%
CHEMBL3524 P56524 Histone deacetylase 4 86.21% 92.97%
CHEMBL4588 P22894 Matrix metalloproteinase 8 85.77% 94.66%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 84.29% 93.00%
CHEMBL5203 P33316 dUTP pyrophosphatase 83.29% 99.18%
CHEMBL3310 Q96DB2 Histone deacetylase 11 82.77% 88.56%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 82.07% 93.03%
CHEMBL1795139 Q8IU80 Transmembrane protease serine 6 81.59% 98.33%
CHEMBL3401 O75469 Pregnane X receptor 80.42% 94.73%

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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Cross-Links

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PubChem 53493058
LOTUS LTS0141324
wikiData Q27137532