iridin

Iridin (Lridin) is major active ingredient of Iris dichotoma which could be used as the drug for pain, inflammation treatment

Iridin (Standard) is a reference standard for research and analysis in studies involving Iridin. Iridin (Lridin) is major active ingredient of Iris dichotoma which could be used as the drug for pain, inflammation treatment

Citreoviridin-C is a useful organic compound for research related to life sciences. The catalog number is T124293 and the CAS number is 74145-78-1.

Citreoviridin, a toxin from Penicillium citreoviride NRRL 2579, inhibits brain synaptosomal Na+/K+-ATPase while significantly stimulating both Na+/K+-ATPase and Mg2+-ATPase activities in microsomes in a dose-dependent manner.

Phenazoviridin is a newly discovered microbial free radical scavenger isolated from the culture medium of Streptomyces HR04. It is an anti-hypoxic compound with strong inhibitory activity against lipid peroxidation in rat brain homogenates and anti-hypoxic activity in mice.

Demethoxyviridin is a potent inhibitor of mammalian Ptdlns 3-kinase, it binds to the catalytic subunit (p110) of the enzyme. Demethoxyviridin is also an antifungal agent.

Rosiridin (6'-O-Deacetylrosiridoside C) has cardioprotective activity.

(1S)-(+)-(10-Camphorsulfonyl)oxaziridine is a useful organic compound for research related to life sciences. The catalog number is T65662 and the CAS number is 104322-63-6.

Viridin, a naturally occurring secondary metabolite and furanosteroid, acts as a potent inhibitor of the lipid kinase PI3K [1] [2].

Cyclophellitol aziridine, an analogue of cyclophenol, serves as a potent inhibitor of β-glucosidase [1].

Griseoviridin is a lactone antibiotic that exhibits activity against Gram-positive and Gram-negative bacteria.

S-2,3-Dicarboxyaziridine is a metabolite that can be isolated from Streptomyces species and exhibits antibacterial activity.

Chaetoviridin A, an azaphilone isolated from Chaetomium globosum, is characterized as 6H-furo[2,3-h]isochromene-6,8(6aH)-dione with substitutions including a chloro group at position 5, a 3-hydroxy-2-methylbutanoyl group at position 9, a methyl group at position 6a, and a 3-methylpent-1-en-1yl group at position 3. It exhibits antifungal activity against plant pathogenic fungi.

Homomoschatoline is an antibacterial isolated from Artabotrys crassifolius.

CB1954(Tretazicar (NSC-115829)), an anticancer prodrug, is activated by NAD(P)H quinone oxidoreductase 2. It is converted in the presence of the enzyme NQO2 and co-substrate caricotamide ( EP-0152R) (EP) into a potent cytotoxic bifunctional alkylating agent.