I0661

(−)-Indolactam V

≥96% (HPLC)

• Synonim(y): (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
• Wzór empiryczny (zapis Hilla): C₁₇H₂₃N₃O₂
• Numer CAS: 90365-57-4
• Masa cząsteczkowa: 301.38
• NACRES: NA.77
• PubChem Substance ID: 329815323
• UNSPSC Code: 12352200
• MDL number: MFCD00151197
• Assay: ≥96% (HPLC)
• Form: powder
• Quality level: 100

Właściwości

• Quality Level: 100
• assay: ≥96% (HPLC)
• form: powder
• color: white
• storage temp.: −20°C
• SMILES string: CC(C)[C@@H]1N(C)c2cccc3[nH]cc(C[C@@H](CO)NC1=O)c23
• InChI: 1S/C17H23N3O2/c1-10(2)16-17(22)19-12(9-21)7-11-8-18-13-5-4-6-14(15(11)13)20(16)3/h4-6,8,10,12,16,18,21H,7,9H2,1-3H3,(H,19,22)/t12-,16-/m0/s1
• InChI key: LUZOFMGZMUZSSK-LRDDRELGSA-N

Opis

Biochem/physiol Actions

(−)-Indolactam V is naturally present in Streptoverticillium blastmyceticum. It serves as a precursor to the teleocidin class which are alkaloids.[1] It is a the pharmacophore of lyngbyatoxin and teleocidins.[1]

(-)-Indolactam V is a PKC activator shown to effect differentiation in embryonic stem cells leading to development of pancreatic precursors.

(-)-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.

Features and Benefits

This compound is featured on the PKC page of the Handbook of Receptor Classification and Signal Transduction. To browse other handbook pages, click here.

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Informacja o środkach bezpieczeństwa

• Klasa składowania: 11 - Combustible Solids
• wgk: WGK 3
• flash_point_f: Not applicable
• flash_point_c: Not applicable