CAS 85955-28-8

Fórmula: C18H25NO6

InChI: InChI=1S/C18H25NO6/c1-4-12-9-11(2)18(3,22)17(21)24-10-13-5-7-19(23)8-6-14(15(13)19)25-16(12)20/h4-5,11,14-15,22H,6-10H2,1-3H3/b12-4+/t11-,14-,15-,18-,19?/m1/s1

Chave InChI: PLGBHVNNYDZWGZ-NRTYDQPPSA-N

SMILES: C/C=C/1\C[C@H]([C@@](C(=O)OCC2=CC[N+]3([C@H]2[C@@H](CC3)OC1=O)[O-])(C)O)C

Integerrimine N-oxide

CAS: 85955-28-8

Integerrimine N-oxide is a useful organic compound for research related to life sciences and the catalog number is T124079.

Fórmula: C₁₈H₂₅NO₆

Cor e Forma: Solid

Peso molecular: 351.39

Ref: TM-T124079

Integerrimine N-oxide

CAS: 85955-28-8

Fórmula: C₁₈H₂₅NO₆

Pureza: 95%~99%

Peso molecular: 351.399

Ref: BP-BP6101

Integerrimine N-oxide

CAS: 85955-28-8

Fórmula: C₁₈H₂₅NO₆

Peso molecular: 351.40

Ref: 4Z-I-137002

Integerrimine N-oxide

CAS: 85955-28-8

Natural alkaloid

Fórmula: C₁₈H₂₅NO₆

Pureza: ≥ 90.0 % (HPLC)

Cor e Forma: Powder

Peso molecular: 351.39

Ref: 5G-83969

Integerrimine N-oxide

CAS: 85955-28-8

Fórmula: C₁₈H₂₅NO₆

Peso molecular: 351.4

Ref: BE-RMT13562

Integerrimine N-oxide

Produto Controlado

CAS: 85955-28-8

Fórmula: C₁₈H₂₅NO₆

Cor e Forma: Neat

Peso molecular: 351.394

Ref: TR-I666696

Integerrimine N-oxide

CAS: 85955-28-8

Integerrimine N-oxide is a specialized pyrrolizidine alkaloid derivative, which is primarily extracted from certain plant species such as those in the Senecio genus. As a naturally occurring compound, it results from the oxidative metabolic conversion of integerrimine, a parent alkaloid originally present in these plants. The mode of action of Integerrimine N-oxide involves its capacity to interact with nucleic acids, potentially leading to cytotoxic effects. This action is mediated by metabolic activation in organisms which may convert it into reactive metabolites that can form DNA adducts, causing cellular damage and apoptosis.

Fórmula: C₁₈H₂₅NO₆

Pureza: Min. 95%

Cor e Forma: Powder

Peso molecular: 351.39 g/mol

Ref: 3D-XI161637