For research use only. Not for therapeutic Use.
Dichloroallyl lawsone(Cat No.:I026071)is a chemical compound derived from lawsone, a natural product found in the henna plant (Lawsonia inermis), with added dichloroallyl groups. Lawsone itself is known for its ability to bind to proteins, especially through its reactive ketone group, which can exhibit various biological activities, including antimicrobial and anticancer properties. The addition of dichloroallyl groups enhances its chemical reactivity and potential for interacting with cellular targets. Dichloroallyl lawsone is under investigation for its therapeutic potential in cancer treatment and other diseases, as it may influence cellular pathways related to growth and survival.
CAS Number | 36417-16-0 |
Synonyms | Dichloroallyl lawsone; Dichloroallyllawsone; Dichlorolapachol; Dichlorolawsone; |
Molecular Formula | C13H8Cl2O3 |
Purity | 98% |
Solubility | Soluble in DMSO |
Appearance | Solid powder |
Storage | Dry, dark and at 0 - 4 C for short term (days to weeks) or -20 C for long term (months to years). |
IUPAC Name | 3-(3,3-dichloroprop-2-enyl)-4-hydroxynaphthalene-1,2-dione |
InChI | InChI=1S/C13H8Cl2O3/c14-10(15)6-5-9-11(16)7-3-1-2-4-8(7)12(17)13(9)18/h1-4,6,16H,5H2 |
InChIKey | LWQZLQISFLBSGW-UHFFFAOYSA-N |
SMILES | C1=CC=C2C(=C1)C(=C(C(=O)C2=O)CC=C(Cl)Cl)O |
Reference | 1: Peters GJ. Antipyrimidine effects of five different pyrimidine de novo synthesis inhibitors in three head and neck cancer cell lines. Nucleosides Nucleotides Nucleic Acids. 2018;37(6):329-339. doi: 10.1080/15257770.2018.1460479. Epub 2018 May 3. PubMed PMID: 29723133. |
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