Article No
BVT-0440-M005
Specifications
| CAS No | 25908-26-3 |
| MW | 518.5 |
| Article No | BVT-0440-M005 |
| Country Availability | SE, FI, DK, NO, IS, EE, LV, LT |
| Description | Cephalochromin |
| Supplier | Adipogen Life Sciences |
| Format | Powder |
| Notes | Chemical. CAS: 25908-26-3. Formula: C28H22O10. MW: 518.5. Isolated from Pseudoanguillospora sp. (strain 6577). Mycotoxin. Bis(naphtha-gamma-pyrone) derivative similar to chaetochromin and ustilaginoidin. Antibiotic. Antibacterial, antifungal and anti-algal compound. Antitumor and cytotoxic compound. Calmodulin-sensitive PDE activity inhibitor. Inhibits NO production by activated macrophages. Selective Fabl (bacterial enoyl-acyl carrier protein (ACP) reductase) inhibitor. Inducer of G0/G1 cell cycle arrest and apoptosis in human A549 cells.|Mycotoxin. Bis(naphtha-gamma-pyrone) derivative similar to chaetochromin and ustilaginoidin [1, 3]. Antibiotic [1]. Antibacterial, antifungal and anti-algal compound [1, 7]. Antitumor and cytotoxic compound [2]. Calmodulin-sensitive PDE activity inhibitor [4]. Inhibits NO production by activated macrophages [5]. Selective Fabl (bacterial enoyl-acyl carrier protein (ACP) reductase) inhibitor [6]. Inducer of G0/G1 cell cycle arrest and apoptosis in human A549 cells [8]. |
| Molecular Formula | C28H22O10 |
| Alias Names | Cefalochromin; NSC201419; NSC627953; Antibiotic Sch45752; 2,2',3,3'-Tetrahydro-5,5',6,6',8,8'-hexahydroxy-2,2'-dimethyl-9,9'-bi[4H-naphtho[2,3-b]pyran]-4,4'-dione |
| Product Type | Chemicals & Biochemicals |
| Purity | >98% |
| Research area | Microbiology |
| Shipping Information | RT |
| Size | 5 mg |
| Solubility | Soluble in DMSO, methanol, acetone or dichloromethane. |
| Stability | Stable for at least 1 year after receipt when stored at -20°C. Store solutions at -20°C in the dark. |
| Storage | -20°C, 4°C |
| Technical Specifications | Chemical. CAS: 25908-26-3. Formula: C28H22O10. MW: 518.5. Isolated from Pseudoanguillospora sp. (strain 6577). Mycotoxin. Bis(naphtha-gamma-pyrone) derivative similar to chaetochromin and ustilaginoidin. Antibiotic. Antibacterial, antifungal and anti-algal compound. Antitumor and cytotoxic compound. Calmodulin-sensitive PDE activity inhibitor. Inhibits NO production by activated macrophages. Selective Fabl (bacterial enoyl-acyl carrier protein (ACP) reductase) inhibitor. Inducer of G0/G1 cell cycle arrest and apoptosis in human A549 cells. |
| Product Page Updated | 2024-02-01T08:25:01.492Z |
