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MedKoo Cat#: 145919 | Name: Tartaramide

Description:

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

ASP-9831 is a small molecule being researched for its potential in treating various cancers, particularly by targeting specific enzymes involved in tumor progression. It works by inhibiting certain proteases that are critical for the growth and metastasis of cancer cells. The mechanism of ASP-9831 involves blocking the activity of these enzymes, which disrupts cancer cell survival and promotes cell death. Due to its targeted action, ASP-9831 is being studied as a potential therapeutic agent for oncology, with a focus on improving cancer treatment outcomes.

Chemical Structure

Tartaramide
Tartaramide
CAS#634-63-9

Theoretical Analysis

MedKoo Cat#: 145919

Name: Tartaramide

CAS#: 634-63-9

Chemical Formula: C4H8N2O4

Exact Mass: 148.0500

Molecular Weight: 148.12

Elemental Analysis: C, 32.44; H, 5.44; N, 18.91; O, 43.21

Price and Availability

This product is currently not in stock but may be available through custom synthesis. To ensure cost efficiency, the minimum order quantity is 1 gram. The estimated lead time is 2 to 4 months, with pricing dependent on the complexity of the synthesis (typically high for intricate chemistries). Quotes for quantities below 1 gram will not be provided. To request a quote, please click the button below. Note: If this product becomes available in stock in the future, pricing will be listed accordingly.
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Related CAS #
No Data
Synonym
Tartaramide; NSC-38709; NSC 38709; NSC38709;
IUPAC/Chemical Name
(2R,3R)-2,3-dihydroxysuccinamide
InChi Key
GRMNJXQBRPJVQV-JCYAYHJZSA-N
InChi Code
1S/C4H8N2O4/c5-3(9)1(7)2(8)4(6)10/h1-2,7-8H,(H2,5,9)(H2,6,10)/t1-,2-/m1/s1
SMILES Code
NC(=O)[C@H](O)[C@@H](O)C(N)=O
Appearance
To be determined
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

Preparing Stock Solutions

The following data is based on the product molecular weight 148.12 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
1: Konno H, Sasaki M, Sano H, Osawa K, Nosaka K, Yano S. The Hydrophobicity and Antifungal Potentiation of Burkholdine Analogues. Molecules. 2022 Feb 10;27(4):1191. doi: 10.3390/molecules27041191. PMID: 35208979; PMCID: PMC8877233. 2: Meng Y, Xiao Q, Bai JY, Xiao X, Zhang S, Zhu XY, Cheng GF, Yin DL. Resolution and chiral recognition of muscone as well as actions on neural system. J Asian Nat Prod Res. 2014 Dec;16(12):1166-70. doi: 10.1080/10286020.2014.996141. Epub 2015 Jan 6. PMID: 25559500. 3: Smith RJ, Capaldi RA, Muchmore D, Dahlquist F. Cross-linking of ubiquinone cytochrome c reductase (complex III) with periodate-cleavable bifunctional reagents. Biochemistry. 1978 Sep 5;17(18):3719-23. doi: 10.1021/bi00611a007. PMID: 212103. 4: Lee CC, Liu Y, Reineke TM. General structure-activity relationship for poly(glycoamidoamine)s: the effect of amine density on cytotoxicity and DNA delivery efficiency. Bioconjug Chem. 2008 Feb;19(2):428-40. doi: 10.1021/bc7001659. Epub 2008 Jan 16. PMID: 18197609. 5: Coggins JR, Lumsden J, Malcolm AD. A study of the quaternary structure of Escherichia coli RNA polymerase using bis(imido esters). Biochemistry. 1977 Mar 22;16(6):1111-6. doi: 10.1021/bi00625a013. PMID: 321015. 6: Oxelbark J, Sellén IB. Effects from hydrogen bonding and rigidity on selectivity in tartaric acid-based chiral selectors for enantioselective liquid chromatography. Chirality. 2003 Nov;15(9):787-93. doi: 10.1002/chir.10299. PMID: 14556216. 7: Ring D, Cole RD. Chemical cross-linking of H1 histone to the nucleosomal histones. J Biol Chem. 1979 Nov 25;254(22):11688-95. PMID: 500667. 8: van Heyningen S. Activity of covalently cross-linked cholera toxin with the adenylate cyclase of intact and lysed pigeon erythrocytes. Biochem J. 1977 Dec 15;168(3):457-63. doi: 10.1042/bj1680457. PMID: 606247; PMCID: PMC1183793.