ISF402
Explore a selection of our essential drug information below, or:
Identification
- Generic Name
- ISF402
- DrugBank Accession Number
- DB06315
- Background
ISF402 is an investigational peptide tetramer which helps dispersal of insulin via zinc chelation, therefore allowing insulin hexamers to break free.
- Type
- Small Molecule
- Groups
- Investigational
- Structure
- Weight
- Average: 469.499
Monoisotopic: 469.228496366 - Chemical Formula
- C19H31N7O7
- Synonyms
- Not Available
Pharmacology
- Indication
Investigated for use/treatment in diabetes mellitus type 2.
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- Pharmacodynamics
Not Available
- Mechanism of action
Insulin is released from the pancreas as hexamers. ISF402, a naturally occurring peptide tetramer, helps dispersal of insulin by allowing the insulin molecules to break free. As single molecules, the insulin is immediately available to bind to receptors on the liver, signalling the liver to take up and store sugar molecules from the blood. ISF402 also amplifies the signal generated by the receptors so that less insulin is needed for the liver's response. [Dia B Tech Website]
Target Actions Organism UInsulin Not Available Humans - Absorption
Not Available
- Volume of distribution
Not Available
- Protein binding
Not Available
- Metabolism
- Not Available
- Route of elimination
Not Available
- Half-life
Not Available
- Clearance
Not Available
- Adverse Effects
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- Toxicity
Not Available
- Pathways
- Not Available
- Pharmacogenomic Effects/ADRs
- Not Available
Interactions
- Drug Interactions
- This information should not be interpreted without the help of a healthcare provider. If you believe you are experiencing an interaction, contact a healthcare provider immediately. The absence of an interaction does not necessarily mean no interactions exist.Not Available
- Food Interactions
- Not Available
Categories
- Drug Categories
- Classification
- Not classified
- Affected organisms
- Not Available
Chemical Identifiers
- UNII
- Not Available
- CAS number
- 484649-95-8
- InChI Key
- BYWLSTFTCYEFLE-GIEZYDSUSA-N
- InChI
- InChI=1S/C19H31N7O7/c1-8(2)14(21)17(30)24-11(4-10-6-22-7-23-10)16(29)26-15(9(3)27)18(31)25-12(19(32)33)5-13(20)28/h6-9,11-12,14-15,27H,4-5,21H2,1-3H3,(H2,20,28)(H,22,23)(H,24,30)(H,25,31)(H,26,29)(H,32,33)/t9-,11+,12+,14+,15+/m1/s1
- IUPAC Name
- SMILES
- [H][C@](C)(O)[C@]([H])(\N=C(/O)[C@]([H])(CC1=CN=CN1)\N=C(/O)[C@@]([H])(N)C(C)C)C(\O)=N\[C@@]([H])(CC(O)=N)C(O)=O
References
- General References
- Paule SG, Nikolovski B, Ludeman J, Gray RE, Spiccia L, Zimmet PZ, Myers MA: Ability of GHTD-amide and analogs to enhance insulin activity through zinc chelation and dispersal of insulin oligomers. Peptides. 2009 Jun;30(6):1088-97. doi: 10.1016/j.peptides.2009.02.020. Epub 2009 Mar 20. [Article]
- External Links
- ChemSpider
- 88297866
Clinical Trials
- Clinical Trials
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Pharmacoeconomics
- Manufacturers
- Not Available
- Packagers
- Not Available
- Dosage Forms
- Not Available
- Prices
- Not Available
- Patents
- Not Available
Properties
- State
- Solid
- Experimental Properties
- Not Available
- Predicted Properties
Property Value Source - Predicted ADMET Features
- Not Available
Spectra
- Mass Spec (NIST)
- Not Available
- Spectra
- Not Available
- Chromatographic Properties
Collision Cross Sections (CCS)
Not Available
Targets
- Kind
- Protein
- Organism
- Humans
- Pharmacological action
- Unknown
- General Function
- Insulin decreases blood glucose concentration. It increases cell permeability to monosaccharides, amino acids and fatty acids. It accelerates glycolysis, the pentose phosphate cycle, and glycogen synthesis in liver
- Specific Function
- hormone activity
- Gene Name
- INS
- Uniprot ID
- P01308
- Uniprot Name
- Insulin
- Molecular Weight
- 11980.795 Da
Drug created at March 19, 2008 16:24 / Updated at August 10, 2024 03:44