11-Ketofistularin 3

Details

Top
Internal ID aa817205-c4f1-44d4-ba27-5cd7e5867da7
Taxonomy Benzenoids > Phenol ethers
IUPAC Name (5R,6S)-7,9-dibromo-N-[2-[3,5-dibromo-4-[3-[[(5S,6R)-7,9-dibromo-6-hydroxy-8-methoxy-1-oxa-2-azaspiro[4.5]deca-2,7,9-triene-3-carbonyl]amino]-2-oxopropoxy]phenyl]-2-hydroxyethyl]-6-hydroxy-8-methoxy-1-oxa-2-azaspiro[4.5]deca-2,7,9-triene-3-carboxamide
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C31H28Br6N4O11/c1-48-24-16(34)5-30(26(44)21(24)36)7-18(40-51-30)28(46)38-9-13(42)11-50-23-14(32)3-12(4-15(23)33)20(43)10-39-29(47)19-8-31(52-41-19)6-17(35)25(49-2)22(37)27(31)45/h3-6,20,26-27,43-45H,7-11H2,1-2H3,(H,38,46)(H,39,47)/t20?,26-,27+,30+,31-/m0/s1
InChI Key SGBKFQBILVXVCY-BCUNMAEHSA-N
Popularity 3 references in papers

Physical and Chemical Properties

Top
Molecular Formula C31H28Br6N4O11
Molecular Weight 1112.00 g/mol
Exact Mass 1111.67934 g/mol
Topological Polar Surface Area (TPSA) 207.00 Ų
XlogP 2.20
Atomic LogP (AlogP) 4.27
H-Bond Acceptor 13
H-Bond Donor 5
Rotatable Bonds 12

Synonyms

Top
(5R,6S)-7,9-dibromo-N-[2-[3,5-dibromo-4-[3-[[(5S,6R)-7,9-dibromo-6-hydroxy-8-methoxy-1-oxa-2-azaspiro[4.5]deca-2,7,9-triene-3-carbonyl]amino]-2-oxopropoxy]phenyl]-2-hydroxyethyl]-6-hydroxy-8-methoxy-1-oxa-2-azaspiro[4.5]deca-2,7,9-triene-3-carboxamide

2D Structure

Top
2D Structure of 11-Ketofistularin 3

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9755 97.55%
Caco-2 - 0.8533 85.33%
Blood Brain Barrier - 0.7750 77.50%
Human oral bioavailability + 0.5286 52.86%
Subcellular localzation Mitochondria 0.5862 58.62%
OATP2B1 inhibitior - 0.5707 57.07%
OATP1B1 inhibitior + 0.8891 88.91%
OATP1B3 inhibitior + 0.9375 93.75%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior + 0.9023 90.23%
P-glycoprotein inhibitior + 0.7497 74.97%
P-glycoprotein substrate + 0.6515 65.15%
CYP3A4 substrate + 0.6868 68.68%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7799 77.99%
CYP3A4 inhibition - 0.5344 53.44%
CYP2C9 inhibition - 0.6750 67.50%
CYP2C19 inhibition - 0.6005 60.05%
CYP2D6 inhibition - 0.8529 85.29%
CYP1A2 inhibition - 0.6625 66.25%
CYP2C8 inhibition + 0.6435 64.35%
CYP inhibitory promiscuity - 0.6751 67.51%
UGT catelyzed - 0.6841 68.41%
Carcinogenicity (binary) - 0.6610 66.10%
Carcinogenicity (trinary) Non-required 0.4799 47.99%
Eye corrosion - 0.9803 98.03%
Eye irritation - 0.9065 90.65%
Skin irritation - 0.7626 76.26%
Skin corrosion - 0.9199 91.99%
Ames mutagenesis - 0.6200 62.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6457 64.57%
Micronuclear + 0.8500 85.00%
Hepatotoxicity - 0.5546 55.46%
skin sensitisation - 0.8185 81.85%
Respiratory toxicity + 0.7778 77.78%
Reproductive toxicity + 0.8556 85.56%
Mitochondrial toxicity + 0.7875 78.75%
Nephrotoxicity - 0.7150 71.50%
Acute Oral Toxicity (c) III 0.5868 58.68%
Estrogen receptor binding + 0.7990 79.90%
Androgen receptor binding + 0.6965 69.65%
Thyroid receptor binding + 0.5744 57.44%
Glucocorticoid receptor binding + 0.6413 64.13%
Aromatase binding + 0.6700 67.00%
PPAR gamma + 0.7086 70.86%
Honey bee toxicity - 0.7921 79.21%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.5700 57.00%
Fish aquatic toxicity + 0.8527 85.27%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 99.35% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 98.90% 96.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 97.62% 85.14%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 97.31% 94.45%
CHEMBL240 Q12809 HERG 96.75% 89.76%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 93.90% 95.17%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 93.80% 94.00%
CHEMBL3401 O75469 Pregnane X receptor 93.20% 94.73%
CHEMBL3060 Q9Y345 Glycine transporter 2 92.23% 99.17%
CHEMBL2581 P07339 Cathepsin D 91.83% 98.95%
CHEMBL221 P23219 Cyclooxygenase-1 91.56% 90.17%
CHEMBL4208 P20618 Proteasome component C5 91.48% 90.00%
CHEMBL3437 Q16853 Amine oxidase, copper containing 88.13% 94.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.42% 95.56%
CHEMBL2535 P11166 Glucose transporter 86.02% 98.75%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 85.94% 96.00%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 85.88% 91.07%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 84.60% 95.89%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 81.14% 90.71%
CHEMBL2885 P07451 Carbonic anhydrase III 80.75% 87.45%
CHEMBL1907598 P05106 Integrin alpha-V/beta-3 80.58% 95.71%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 80.30% 92.62%
CHEMBL1907602 P06493 Cyclin-dependent kinase 1/cyclin B1 80.28% 91.24%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 80.11% 100.00%

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 23427264
LOTUS LTS0171526
wikiData Q105252219