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About This Item
Empirical Formula (Hill Notation):
C15H11ClO5
CAS Number:
Molecular Weight:
306.70
EC Number:
205-127-7
UNSPSC Code:
12352100
PubChem Substance ID:
Beilstein/REAXYS Number:
3922945
MDL number:
InChI key
YPVZJXMTXCOTJN-UHFFFAOYSA-N
InChI
1S/C15H10O5.ClH/c16-9-3-1-8(2-4-9)15-13(19)7-11-12(18)5-10(17)6-14(11)20-15;/h1-7H,(H3-,16,17,18,19);1H
SMILES string
[Cl-].Oc1ccc(cc1)-c2[o+]c3cc(O)cc(O)c3cc2O
grade
purum
impurities
4-6% water
storage temp.
2-8°C
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Application
Involved in pharmacological studies investigating the use of flavonoids as inhibitors of CD38
Antioxidant and anthocyanidin:
Antioxidant and anthocyanidin:
- Found in various natural sources evaluated for inhibitory effects on colon and liver cancer cells
- Used as hyroperoxide and hydrogen peroxide scavenging substance
- Used to study relationship between structure, antioxidant capacity and redox potentials
- Studied to determine the mechanism of radical-scavenging
Biochem/physiol Actions
Antioxidant and anthocyanidin.
Packaging
Bottomless glass bottle. Contents are inside inserted fused cone.
Regulatory Information
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Sridaran Dhivya et al.
Integrative cancer therapies, 15(4), 525-534 (2016-05-06)
Hypothesis Anthocyanins possess well-known biological effects and suppress DNA damage induced by therapeutic topoisomerase poisons. Our study focusses on the modulatory effects of anthocyanidins-malvidin (MAL) and pelargonidin (PEL)-on topoisomerase II poison mitoxantrone (MXT)-induced cytotoxicity and genotoxicity in in vitro and
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