487-21-8
487-21-8
Chemical Structure
Pteridine-2,4(1H,3H)-dione
- CAS No.: 487-21-8
- Formula:C6H4N4O2
- Molecular Weight:164.12
IUPAC Name: pteridine-2,4(1H,3H)-dione
InChIKey: UYEUUXMDVNYCAM-UHFFFAOYSA-N
SMILES: O=C(N1)NC2=NC=CN=C2C1=O
Biological Activity: Pteridine-2,4 (1H,3H)-dione is a pteridine derivative (xanthopterin) and a sulfur-containing pteridine compound (2,4-dimercaptopyrimidine). Pteridine-2,4 (1H,3H)-dione possesses metal-binding ability, and forms closed-shell (ionic) interactions with palladium via sulfur and nitrogen atoms. Pteridine-2,4 (1H,3H)-dione derivates can be used in studies related to neuroblastoma, glioma and breast cancer[1][2].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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Pteridine-2,4(1H,3H)-dione | 99.86% | Pteridine-2,4 (1H,3H)-dione is a pteridine derivative (xanthopterin) and a sulfur-containing pteridine compound (2,4-dimercaptopyrimidine). Pteridine-2,4 (1H,3H)-dione possesses metal-binding ability, and forms closed-shell (ionic) interactions with palladium via sulfur and nitrogen atoms. Pteridine-2,4 (1H,3H)-dione derivates can be used in studies related to neuroblastoma, glioma and breast cancer. | ||||||||||||||||||||
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Pteridine-2,4(1H,3H)-dione (Standard) | ≥98% | Pteridine-2,4(1H,3H)-dione is an endogenous metabolite. | ||||||||||||||||||||
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References
- [1]. Carmona-Martínez V, et al. Therapeutic potential of pteridine derivatives: A comprehensive review. Med Res Rev. 2019;39(2):461-516. [Content Brief]
- [2]. Illán-Cabeza N A, et al. XRD and DFT-modelized structures of a pteridine-2, 4 (1H, 3H)-dithione/N, N′-dimethylformamide H-bonded cluster (2: 2). MO study of the coordination ability[J]. Journal of molecular modeling, 2012, 18(2): 815-824.
