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(-)-INDOLACTAM V

(-)-INDOLACTAM V Structure
(-)-INDOLACTAM V
  • CAS No.90365-57-4
  • Chemical Name:(-)-INDOLACTAM V
  • CBNumber:CB2244996
  • Molecular Formula:C17H23N3O2
  • Formula Weight:301.38
  • MOL File:90365-57-4.mol
(-)-INDOLACTAM V Property
  • Boiling point 584.0±50.0 °C(Predicted)
  • Density 1.166±0.06 g/cm3(Predicted)
  • storage temp. -20°C
  • solubility DMSO: >10mg/mL, clear
  • form white powder
  • pka 14.39±0.10(Predicted)
  • color White to light yellow
  • Stability Stable for 1 year from date of purchase as supplied. Solutions in DMSO or ethanol may be stored at -20°C for up to 2 months.
  • FDA UNII 8CIY9O1323
  • UNSPSC Code 12352200
  • NACRES NA.77
Safety
  • WGK Germany  :3
  • RTECS  :UY8547000
Hazard and Precautionary Statements (GHS)
  • Symbol(GHS)
  • Signal wordWarning
  • Hazard statements H315-H319-H335
  • Precautionary statements P261-P264-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P332+P313
(-)-INDOLACTAM V Price More Price(1)
  • Brand: Sigma-Aldrich(India)
  • Product number: I0661
  • Product name : (−)-Indolactam V
  • Purity: ≥96% (HPLC)
  • Packaging: 1MG
  • Price: ₹35744.15
  • Updated: 2022/06/14
  • Buy: Buy

(-)-INDOLACTAM V Chemical Properties,Usage,Production

  • Description Indolactam V (-) (90365-57-4) is a PKC activator acting at the phorbol ester binding site.1,2?Directs differentiation of human and mouse ESCs to pancreatic cells.3?? May be used, along with other agents, to differentiate human iPS cells into glucose-responsive insulin-secreting progeny.4?Increases regulator of G protein signaling 2 (RGS2) protein levels, a protein that regulates GPCR signaling.5
  • Uses (-)-Indolactam V is an indole alkaloid compound which activates protein kinase C (PKC). Weak tumor promoter. Also directs differentiation of human embryonic stem cells, potentially into pancreatic lineage allowing for an effective diabetes therapy.
  • Definition ChEBI: (-)-indolactam V is a 9-membered ring that is a potent protein kinase C activator
  • Biological Activity Protein kinase C activator. Exhibits tumor promoting activity. Directs differentiation of human embryonic stem cells (ESCs) into pancreatic progenitors.
  • Biochem/physiol Actions (-)-Indolactam V is a PKC activator shown to effect differentiation in embryonic stem cells leading to development of pancreatic precursors. It is active in the mouse model.
  • storage -20°C (desiccate)
  • References 1) Fujiki?et al.?(1984),?Structure-activity studies on synthetic analogues (indolactams) of the tumor promoter teleocidin; Gan., 75?866 2) Heikkila and Ackerman (1989),?(-)-Indolactam V activates protein kinase C and induces changes in muscarinic receptor functions in SH-SY5Y human neuroblastoma cells; Biochem. Biophys. Res. Commun,?162?1207 3) Chen?et al.?(2009),?A small molecule that directs differentiation of human ESCs into the pancreatic lineage; Nat. Chem. Biol.,?5?258 4) Thalava?et al. (2011),?Indolactam V/GLP-1-mediated differentiation of human iPS cells into glucose-responsive insulin-secretin progeny; Gene Ther.,?18?283 5) Raveh (2014),?Identification of protein kinase C activation as a novel mechanism for RGS2 protein upregulation through phenotypic screening of natural product extracts; Mol. Pharmacol.,?86?406
(-)-INDOLACTAM V Preparation Products And Raw materials
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(-)-INDOLACTAM V Spectrum
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  • (2S,5S)-5-(Hydroxymethyl)-2-isopropyl-1-methyl-4,5,6,8-tetrahydro-1H-[1,4]diazonino[7,6,5-cd]indol-3(2H)-one
  • ()Indolactam V,( ) Indolactam V
  • (-)-Indolactam V
  • ()-Indolactam V
  • (-)-Indolactam V&nbsp
  • IndolactaM
  • Brn 4711877
  • 3H-Pyrrolo(4,3,2-gh)-1,4-benzodiazonin-3-one, 1,2,4,5,6,8-hexahydro-5-(hydroxymethyl)-1-methyl-2-(1-methylethyl)-, (2S,5S)-
  • 3H-Pyrrolo(4,3,2-gh)-1,4-benzodiazonin-3-one, 1,2,4,5,6,8-hexahydro-5-(hydroxymethyl)-1-methyl-2-(1-methylethyl)-, (2S-(2R*,5R*))-
  • (-)-Ilv
  • (2S,5S)-1,2,4,5,6,8-Hexahydro-5-(hydroxymethyl)-1-methyl-2-(1-methylethyl)-3H-pyrrolo[4,3,2-gh]-1,4-benzodiazonin-3-one
  • 3h-pyrrolo(4,3,2-gh)-1,4-benzodiazonin-3-one,1,2,4,5,6,8-hexahydro-5-(hydroxym
  • (2s-(2r*,5r*))-ethyl)-1-methyl-2-(1-methylethyl)

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