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CNDAC

CAS No.
135598-68-4
Chemical Name:
CNDAC
Synonyms
DFP-10917;2'-Cyano-2'-deoxy-1-(b-D-arabinofuranosyl)cytosine;4-amino-1-(2-cyano-2-deoxy-β-D-arabinofuranosyl)-2(1H)-pyrimidinone;2(1H)-Pyrimidinone, 4-amino-1-(2-cyano-2-deoxy-β-D-arabinofuranosyl)-;4-Amino-1-(2-cyano-2-deoxy-beta-D-arabinofuranosyl)-2(1H)-pyrimidinone
CBNumber:
CB73139601
Molecular Formula:
C10H12N4O4
Molecular Weight:
252.23
MDL Number:
MOL File:
135598-68-4.mol
MSDS File:
SDS
Last updated:2025-04-18 09:52:39
Product description Number Pack Size Price
CNDAC >98% DC9799 250mg $1000

CNDAC Properties

Boiling point 596.9±60.0 °C(Predicted)
Density 1.75±0.1 g/cm3(Predicted)
storage temp. Store at -20°C
solubility Soluble in DMSO
pka 12.78±0.70(Predicted)
FDA UNII 00M634HD2V

CNDAC price

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
DC Chemicals DC9799 CNDAC >98% 135598-68-4 250mg $1000 2021-12-16 Buy
Product number Packaging Price Buy
DC9799 250mg $1000 Buy

CNDAC Chemical Properties,Uses,Production

Uses

CNDAC is a metabolite of the orally active agent Sapacitabine.html" class="link-product" target="_blank">Sapacitabine (HY-16445), and a nucleoside analog. CNDAC induces DNA damage and apoptosis[1][2].

Definition

ChEBI: CNDAC is a pyrimidine 2'-deoxyribonucleoside that is 2'-deoxycytidine having a cyano group in the 2'-position. It is the active metabolite of the anti-cancer drug, sapacitabine which is currently in clinical development for the treatment of hematologic malignancies and solid tumors. It has a role as an antineoplastic agent, a drug metabolite and a DNA synthesis inhibitor. It is a pyrimidine 2'-deoxyribonucleoside and a nitrile.

in vivo

CNDAC (20mg/kg; i.p.; daily for 10 days) shows antitumor activity in mice[4].

Animal Model:CDF1 mice, P388 tumor model[4]
Dosage:20 mg/kg
Administration:Intraperitoneal injection, daily for 10 days
Result:Greatly increased the survival time and survival rate.

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. hin J Cancer. 2012 Aug;31(8):373-80. DOI:10.5732/cjc.012.10077
[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. DOI:10.1155/2012/727683
[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. DOI:10.1038/sj.bjc.6603896
[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. DOI:10.1021/jm00078a006

CNDAC Preparation Products And Raw materials

Raw materials

Preparation Products

CNDAC Suppliers

Global( 20)Suppliers
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TargetMol Chemicals Inc.
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Shanghai Boyle Chemical Co., Ltd. sales@boylechem.com China 2922 55
Beijing Jin Ming Biotechnology Co., Ltd. 010-60605840 18892239720 psaitong@jm-bio.com China 12306 58
Shanghai Biopharmaleader Co., Ltd. +86 18721201413 sales@biopharmaleader.com China 1720 58
Angel Pharmatech, Ltd. 17317130613 3358272972@qq.com China 3272 58
4-Amino-1-(2-cyano-2-deoxy-beta-D-arabinofuranosyl)-2(1H)-pyrimidinone DFP-10917 2(1H)-Pyrimidinone, 4-amino-1-(2-cyano-2-deoxy-β-D-arabinofuranosyl)- 2'-Cyano-2'-deoxy-1-(b-D-arabinofuranosyl)cytosine 4-amino-1-(2-cyano-2-deoxy-β-D-arabinofuranosyl)-2(1H)-pyrimidinone 135598-68-4