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MedicaPharma distributes high-quality active pharmaceutical ingredients (APIs) to hospitals, commercial (compounding) pharmacies, research institutes, and universities worldwide.
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Let us handle your sourcing / supply activities. Highly experienced in sourcing specialty raw pharmaceutical ingredients from niche GMP manufacturers around the world.
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Product Description
Mechanism of action
Carbazochrome (adrenochrome derivative) is a haemostatic compound believed to stabilise capillary endothelium and reduce microvascular bleeding. It suppresses excessive capillary permeability, enhances vascular resistance and modulates local oxidative signalling through redox‑active mechanisms.
Benefits and advantages
Used in microvascular‑bleeding studies, capillary‑permeability modelling, oxidative‑stress pathway research, haemostasis assays and vascular‑endothelium stabilisation analysis.
Side effects and risks
Risks include flushing, headache, mild hypertension, hypersensitivity and rare coagulation disturbances. Handle as a vascular‑active compound.
Datasheet
| Molecular Formula | C16H18N2O7 |
|---|---|
| Molecular Weight | 236.23 g/mol |
| CAS Number | 55987-18-7 |
| Storage Condition | Store in a cool, dry place. Keep container tightly closed. Protect from moisture and light. |
| Solubility | Solubility depends on solvent and conditions (e.g., pH). Please contact us for solvent-specific guidance. |
| Purity | Purity information is available upon request (COA). |
| Synonym | carbazochrome; 69-81-8; Adrenochrome semicarbazone; Adedolon; Adrenostazin |
| IUPAC/Chemical Name | (3,6-dihydroxy-1-methyl-2,3-dihydroindol-5-yl)iminourea |
| InChl Key | SSCSSDNTQJGTJT-UHFFFAOYSA-N |
| InChl Code | InChI=1S/C10H12N4O3/c1-14-4-9(16)5-2-6(12-13-10(11)17)8(15)3-7(5)14/h2-3,9,15-16H,4H2,1H3,(H2,11,17) |
| References |
3D Conformer.
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