Synonym: (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
CAS Number: 90365-57-4
Empirical Formula (Hill Notation): C17H23N3O2
Molecular Weight: 301.38
MDL Number: MFCD00151197
Linear Formula: C17H23N3O2
Product Type: Chemical
| assay |
≥96% (HPLC) |
| color |
white |
| form |
powder |
| 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 |
| Quality Level |
100  |
| SMILES string |
CC(C)[C@@H]1N(C)c2cccc3[nH]cc(C[C@@H](CO)NC1=O)c23 |
| storage temp. |
−20°C |
| Biochem/physiol Actions: |
(-)-Indolactam V is a PKC activator shown to effect differentiation in embryonic stem cells leading to development of pancreatic precursors. |
| 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. |
| Biochem/physiol Actions: |
(−)-Indolactam V is naturally present in Streptoverticillium blastmyceticum. It serves as a precursor to the teleocidin class which are alkaloids. It is a the pharmacophore of lyngbyatoxin and teleocidins. |
| 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 . |
| Packaging: |
1 mg in glass bottle |
| RIDADR |
NONH for all modes of transport |
| WGK Germany |
WGK 3 |
| Flash Point(F) |
Not applicable |
| Flash Point(C) |
Not applicable |
| Purity |
≥96% (HPLC) |
| Storage Temp. |
−20°C |
| UNSPSC |
12352200 |
