Chlorambucil
For Laboratory Research Only. Not for Clinical or Personal Use.
- Availability: 24/48H Stock Items & 2 to 6 Weeks non Stock Items.
- Dry Ice Shipment: No


Chlorambucil
Description:
Chlorambucil (CB-1348), an orally active antineoplastic agent, is a bifunctional alkylating agent belonging to the nitrogen mustard group. Chlorambucil can be used for the research of lymphocytic leukemia, ovarian and breast carcinomas, and Hodgkin’s disease[1][2][3][4].Product Name Alternative:
CB-1348; WR-139013UNSPSC:
12352005Hazard Statement:
H301, H315, H319, H335, H350Target:
DNA Alkylator/CrosslinkerType:
Reference compoundRelated Pathways:
Cell Cycle/DNA DamageApplications:
Cancer-programmed cell deathField of Research:
CancerAssay Protocol:
https://www.medchemexpress.com/Chlorambucil.htmlConcentration:
10mMPurity:
99.84Solubility:
DMSO : ≥ 100 mg/mLSmiles:
O=C(O)CCCC1=CC=C(N(CCCl)CCCl)C=C1Molecular Formula:
C14H19Cl2NO2Molecular Weight:
304.21Precautions:
H301, H315, H319, H335, H350References & Citations:
[1]Guo JX, et al. Synergistic effects of chlorambucil and TRAIL on apoptosis and proliferation of Raji cells. Eur Rev Med Pharmacol Sci. 2017 Oct;21 (20) :4703-4710.|[2]Salem FS, et al. Biochemical and pathological studies on the effects of levamisole and chlorambucil on Ehrlich ascites carcinoma-bearing mice. Vet Ital. 2011 Jan-Mar;47 (1) :89-95.|[3]Mohamed D, et al. Chlorambucil-adducts in DNA analyzed at the oligonucleotide level using HPLC-ESI MS. Chem Res Toxicol. 2009;22 (8) :1435-1446.|[4]Birnbaum AD, et al. Chlorambucil and malignancy. Ophthalmology. 2010;117 (7) :1466-1466.e1.Shipping Conditions:
Room TemperatureStorage Conditions:
-20°C, 3 years; 4°C, 2 years (Powder)Scientific Category:
Reference compound1Clinical Information:
LaunchedCAS Number:
305-03-3
