CAS 85955-28-8

Formula: 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

InChI key: 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.

Formula: C₁₈H₂₅NO₆

Color and Shape: Solid

Molecular weight: 351.39

Ref: TM-T124079

Integerrimine N-oxide

CAS: 85955-28-8

Formula: C₁₈H₂₅NO₆

Purity: 95%~99%

Molecular weight: 351.399

Ref: BP-BP6101

Integerrimine N-oxide

CAS: 85955-28-8

Formula: C₁₈H₂₅NO₆

Molecular weight: 351.40

Ref: 4Z-I-137002

Integerrimine N-oxide

CAS: 85955-28-8

Natural alkaloid

Formula: C₁₈H₂₅NO₆

Purity: ≥ 90.0 % (HPLC)

Color and Shape: Powder

Molecular weight: 351.39

Ref: 5G-83969

Integerrimine N-oxide

CAS: 85955-28-8

Formula: C₁₈H₂₅NO₆

Molecular weight: 351.4

Ref: BE-RMT13562

Integerrimine N-oxide

Controlled Product

CAS: 85955-28-8

Formula: C₁₈H₂₅NO₆

Color and Shape: Neat

Molecular weight: 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.

Formula: C₁₈H₂₅NO₆

Purity: Min. 95%

Color and Shape: Powder

Molecular weight: 351.39 g/mol

Ref: 3D-XI161637