NSC 5302
featured

    WARNING: This product is for research use only, not for human or veterinary use.

Hodoodo CAT#: H464501

CAS#: 2107-76-8

Description: NSC 5302 is a synthetic coumarin with diverse biological activities. It scavenges alkylperoxy radicals and hypochlorous acid (HOCl; IC50 = 2.85 µM) in cell-free assays, as well as inhibits lipid peroxidation in rat liver microsomes, A23187-induced thromboxane B2 (TXB2) generation in isolated rat peritoneal leukocytes, and myeloperoxidase (MPO) activity in a cell-free assay (IC50s = 12, 1, and 1.06 µM, respectively). NSC 5302 also inhibits rat lens aldose reductase (IC50 = 17 µM) and human carbonic anhydrase I (CAI), CAIX, and CAXII with Ki values of 8.4, 0.19, and 6.4 µM, respectively. It inhibits platelet aggregation induced by arachidonic acid with an IC50 value of 45 µM. NSC 5302 inhibits hepatitis C virus (HCV) non-structural protein 5B (NS5B) polymerase (IC50 = 47.2 µM). It is active against H. pylori with an MIC value of 10 µg/ml.


Chemical Structure

img
NSC 5302
CAS# 2107-76-8

Theoretical Analysis

Hodoodo Cat#: H464501
Name: NSC 5302
CAS#: 2107-76-8
Chemical Formula: C10H8O4
Exact Mass: 192.04
Molecular Weight: 192.170
Elemental Analysis: C, 62.50; H, 4.20; O, 33.30

Price and Availability

Size Price Availability Quantity
10mg USD -2 2 Weeks
25mg USD -2 2 Weeks
50mg USD -2 2 Weeks
100mg USD -2 2 Weeks
2g USD -2 2 Weeks
5g USD -2 2 Weeks
250mg USD 220 2 Weeks
500mg USD 350 2 Weeks
1g USD 540 2 Weeks
Bulk inquiry

Synonym: NSC 5302; NSC-5302; NSC5302; 5,7-Dihydroxy-4-methylcoumarin;

IUPAC/Chemical Name: 5,7-dihydroxy-4-methyl-2H-chromen-2-one

InChi Key: QNVWGEJMXOQQPM-UHFFFAOYSA-N

InChi Code: InChI=1S/C10H8O4/c1-5-2-9(13)14-8-4-6(11)3-7(12)10(5)8/h2-4,11-12H,1H3

SMILES Code: O=C1OC2=C(C(O)=CC(O)=C2)C(C)=C1

Appearance: Solid powder

Purity: >98% (or refer to the Certificate of Analysis)

Shipping Condition: Shipped under ambient temperature as non-hazardous chemical. This product is stable enough for a few weeks during ordinary shipping and time spent in Customs.

Storage Condition: Dry, dark and at 0 - 4 C for short term (days to weeks) or -20 C for long term (months to years).

Solubility: To be determined

Shelf Life: >2 years if stored properly

Drug Formulation: To be determined

Stock Solution Storage: 0 - 4 C for short term (days to weeks), or -20 C for long term (months).

HS Tariff Code: 2934.99.9001

More Info:

Biological target:
In vitro activity:
In vivo activity:

Solubility Data

Solvent Max Conc. mg/mL Max Conc. mM
Solubility
DMF 30.0 156.00
DMSO 30.0 156.00
DMSO:PBS (pH 7.2) (1:3) 0.3 1.30
Ethanol 20.0 104.00

Preparing Stock Solutions

The following data is based on the product molecular weight 192.17 Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.

Recalculate based on batch purity %
Concentration / Solvent Volume / Mass 1 mg 5 mg 10 mg
1 mM 1.15 mL 5.76 mL 11.51 mL
5 mM 0.23 mL 1.15 mL 2.3 mL
10 mM 0.12 mL 0.58 mL 1.15 mL
50 mM 0.02 mL 0.12 mL 0.23 mL
Formulation protocol:
In vitro protocol:
In vivo protocol:

Molarity Calculator

Calculate the mass, volume, or concentration required for a solution.
=
x
x
g/mol

*When preparing stock solutions always use the batch-specific molecular weight of the product found on the vial label and SDS / CoA (available online).

Reconstitution Calculator

The reconstitution calculator allows you to quickly calculate the volume of a reagent to reconstitute your vial. Simply enter the mass of reagent and the target concentration and the calculator will determine the rest.

=
÷

Dilution Calculator

Calculate the dilution required to prepare a stock solution.
x
=
x

1: Kabeya LM, Fuzissaki CN, Andrade MF, Azzolini AE, Taleb-Contini SH, Vermelho RB, Lopes JL, Lucisano-Valim YM. 4-methylcoumarin derivatives inhibit human neutrophil oxidative metabolism and elastase activity. J Med Food. 2013 Aug;16(8):692-700. doi: 10.1089/jmf.2012.0184. Epub 2013 Aug 1. PMID: 23905650; PMCID: PMC3751208.

2: Macáková K, Řeháková Z, Mladěnka P, Karlíčková J, Filipský T, Říha M, Prasad AK, Parmar VS, Jahodář L, Pávek P, Hrdina R, Saso L. In vitro platelet antiaggregatory properties of 4-methylcoumarins. Biochimie. 2012 Dec;94(12):2681-6. doi: 10.1016/j.biochi.2012.09.006. Epub 2012 Sep 17. PMID: 22996069.

3: Xue B, Zhou L, Liu J, Yu R. Biotransformation of hydroxycoumarin derivatives by cultured suspension cells of Catharanthus roseus. Pharmazie. 2012 May;67(5):467-71. PMID: 22764584.

4: Kancheva VD, Saso L, Boranova PV, Khan A, Saroj MK, Pandey MK, Malhotra S, Nechev JZ, Sharma SK, Prasad AK, Georgieva MB, Joseph C, DePass AL, Rastogi RC, Parmar VS. Structure-activity relationship of dihydroxy-4-methylcoumarins as powerful antioxidants: correlation between experimental & theoretical data and synergistic effect. Biochimie. 2010 Sep;92(9):1089-100. doi: 10.1016/j.biochi.2010.06.012. Epub 2010 Jun 19. PMID: 20600568.

5: Esquivelzeta-Rabell M, Peon J, Cuevas G. Rotational diffusion of dihydroxy coumarins: Effect of OH groups and their relative position on solute-solvent interactions. J Phys Chem B. 2009 Jun 25;113(25):8599-606. doi: 10.1021/jp9010058. PMID: 19489576.

6: Céspedes CL, Avila JG, Martínez A, Serrato B, Calderón-Mugica JC, Salgado- Garciglia R. Antifungal and antibacterial activities of Mexican tarragon (Tagetes lucida). J Agric Food Chem. 2006 May 17;54(10):3521-7. doi: 10.1021/jf053071w. PMID: 19127719.

7: Sharma RK, Pande V, Ramos MJ, Rajor HK, Chopra S, Meguro K, Inoue J, Otsuka M. Inhibitory activity of polyhydroxycarboxylate chelators against recombinant NF-kappaB p50 protein-DNA binding. Bioorg Chem. 2005 Apr;33(2):67-81. doi: 10.1016/j.bioorg.2004.12.001. PMID: 15788163.

8: Kurosaki H, Sharma RK, Otsuka M, Goto M. Crystal structure of 7,8-dihydroxy-4-methylcoumarin. Anal Sci. 2003 Apr;19(4):647-8. doi: 10.2116/analsci.19.647. PMID: 12725413.

9: Hoult JR, Payá M. Pharmacological and biochemical actions of simple coumarins: natural products with therapeutic potential. Gen Pharmacol. 1996 Jun;27(4):713-22. doi: 10.1016/0306-3623(95)02112-4. PMID: 8853310.

10: Hoult JR, Forder RA, de las Heras B, Lobo IB, Payá M. Inhibitory activity of a series of coumarins on leukocyte eicosanoid generation. Agents Actions. 1994 Aug;42(1-2):44-9. doi: 10.1007/BF02014299. PMID: 7847183.

11: Payá M, Halliwell B, Hoult JR. Interactions of a series of coumarins with reactive oxygen species. Scavenging of superoxide, hypochlorous acid and hydroxyl radicals. Biochem Pharmacol. 1992 Jul 22;44(2):205-14. doi: 10.1016/0006-2952(92)90002-z. PMID: 1322662.

12: Hausen BM, Berger M. The sensitizing capacity of coumarins (III). Contact Dermatitis. 1989 Sep;21(3):141-7. doi: 10.1111/j.1600-0536.1989.tb04726.x. PMID: 2529098.