IUPAC/Chemical Name
p-(p-((5-Thio-beta-D-xylopyranosyl)thio)benzoyl)benzonitrile
InChi Key
IMAFEPKOGMHYNH-LULLPPNCSA-N
InChi Code
InChI=1S/C19H17NO4S2/c20-9-11-1-3-12(4-2-11)16(22)13-5-7-14(8-6-13)26-19-18(24)17(23)15(21)10-25-19/h1-8,15,17-19,21,23-24H,10H2/t15-,17+,18-,19+/m1/s1
SMILES Code
O[C@@H]1CS[C@@H](Sc2ccc(cc2)C(=O)c3ccc(cc3)C#N)[C@H](O)[C@H]1O
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
Preparing Stock Solutions
The following data is based on the
product
molecular weight
387.47
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.
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 |
1. Masson PJ, Coup D, Millet J, Brown NL. The effect of the beta-D-xyloside naroparcil on circulating plasma glycosaminoglycans. An explanation for its known antithrombotic activity in the rabbit. J Biol Chem. 1995 Feb 10;270(6):2662-8. doi: 10.1074/jbc.270.6.2662. PMID: 7852334.
2. Steg PG, Ziol M, Tahlil O, Robert C, Masson P, Pruneau D, Bruneval P, Bélichard P. Reduction of intimal hyperplasia by naroparcil, a 4-methylumbelliferyl beta-D-xyloside analogue, after arterial injury in the hypercholesterolemic rabbit. Circ Res. 1995 Nov;77(5):919-26. doi: 10.1161/01.res.77.5.919. PMID: 7554145.
3 .Millet J, Theveniaux J, Brown NL. The venous antithrombotic profile of naroparcil in the rabbit. Thromb Haemost. 1994 Dec;72(6):874-9. PMID: 7740457.
4. Masson P, Theveniaux J, Coup D, Grégoire T, Vaillot M, Dupouy D, Sié P, Boneu B, Millet J. Further studies on the mechanism for the antithrombotic effects of naroparcil, an orally active thiozyloside compound. Thromb Haemost. 1999 Jun;81(6):945-50. PMID: 10404773.