CNDAC hydrochloride salt form · hydrochloride · Parent CNDAC hydrochloride
CNDAC hydrochloride is a metabolite of the orally active agent Sapacitabine , and a nucleoside analog.
For research use only. Not for human or veterinary use.
Research area
Cancer
Purity >98%
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CNDAC hydrochloride structure
CAS No.: 134665-72-8
Pack sizes & pricing
Description
CNDAC hydrochloride is a metabolite of the orally active agent Sapacitabine , and a nucleoside analog. CNDAC hydrochloride induces DNA damage and apoptosis .
Biological activity
CNDAC hydrochloride is a metabolite of Sapacitabine, and it is a nucleoside analog. CNDAC hydrochloride induces DNA damage and apoptosis. CNDAC (20mg/kg; i.p.; daily for 10 days) greatly increased the survival time and survival rate in CDF1 mice P388 tumor model.
Identifiers
- SMILES
-
Cl[H].NC1=NC(=O)N(C=C1)[C@@H]1O[C@H](CO)[C@@H](O)[C@@H]1C#N - InChIKey
-
PKGUOXDXRLGZBN-KUAPJGQRSA-N
Specifications
- MW (average)
- 288.6880
- Formula
- C10H13ClN4O4
- CAS No.
- 134665-72-8
- Physical state
- Solid
- Color
- White to off-white
- Shipping
- 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
- Powder 4°C, sealed storage, away from moisture
Solubility
Soluble in DMSO
Documents
References
[1]. Liu XJ, et al. Sapacitabine, the prodrug of CNDAC, is a nucleoside analog with a unique action mechanism of inducing DNA strand breaks. Chin J Cancer. 2012 Aug;31(8):373-80.
[2]. Jagan S, et al. Bone Marrow and Peripheral Blood AML Cells Are Highly Sensitive to CNDAC, the Active Form of Sapacitabine. Adv Hematol. 2012;2012:727683.
[3]. Serova M, et al. Antiproliferative effects of sapacitabine (CYC682), a novel 2'-deoxycytidine-derivative, in human cancer cells. Br J Cancer. 2007 Sep 3;97(5):628-36.
[4]. Azuma A, et al. Nucleosides and nucleotides. 122. 2'-C-cyano-2'-deoxy-1-beta-D-arabinofuranosylcytosine and its derivatives. A new class of nucleoside with a broad antitumor spectrum. J Med Chem. 1993 Dec 24;36(26):4183-9.
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