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Carmustine (CAS 154-93-8)

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Alternate Names:
1,3-bis(2-chloroethyl)-1-nitrosourea; Nitrumon; Carmubris; Gliadel
Application:
Carmustine is a DNA alkylating and cross-linking agent used in the treatment of brain tumors and various other malignant neoplasms
CAS Number:
154-93-8
Purity:
≥96%
Molecular Weight:
214.05
Molecular Formula:
C5H9Cl2N3O2
Supplemental Information:
This is classified as a Dangerous Good for transport and may be subject to additional shipping charges.
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Carmustine, classified within the antineoplastic nitrosourea compounds, exhibits a dual-functional mechanism, engaging in both alkylating and carbamoylating activities. Its cytotoxic prowess is primarily attributed to its capacity for inducing interstrand DNA cross-linking, which interrupts the replication and transcription processes critical for cell survival. Beyond its direct action on DNA, Carmustine disrupts cellular redox balance by inhibiting key enzymes such as glutathione reductase, trypanothione reductase, and lipoamide dehydrogenase (DLD). These enzymes are pivotal in maintaining the antioxidant defense mechanism within cells, and their inhibition by Carmustine compromises cellular ability to detoxify reactive oxygen species, leading to enhanced oxidative stress. As part of the nitrogen mustard family, Carmustine′s alkylating property further contributes to its efficacy in research applications, especially in studies focused on the molecular mechanisms of cytotoxicity and the cellular response to DNA damage. Its diverse mechanisms of action make Carmustine a valuable compound for investigating the intricacies of cellular metabolism and the DNA repair system, shedding light on the molecular pathways that underpin cell proliferation and survival.


Carmustine (CAS 154-93-8) References

  1. Carmustine wafers: localized delivery of chemotherapeutic agents in CNS malignancies.  |  Lin, SH. and Kleinberg, LR. 2008. Expert Rev Anticancer Ther. 8: 343-59. PMID: 18366283
  2. Carmustine wafer implantation when surgical cavity is communicating with cerebral ventricles: technical considerations on a clinical series.  |  Della Puppa, A., et al. 2011. World Neurosurg. 76: 156-9; discussion 67-8. PMID: 21839967
  3. Carmustine infusion reactions are more common with rapid administration.  |  Janson, B., et al. 2012. Support Care Cancer. 20: 2531-5. PMID: 22252549
  4. Purification and characterization of lipoamide dehydrogenase from Trypanosoma cruzi.  |  Lohrer, H. and Krauth-Siegel, RL. 1990. Eur J Biochem. 194: 863-9. PMID: 2269305
  5. Modeling mass transfer from carmustine-loaded polymeric implants for malignant gliomas.  |  Pereira, DY., et al. 2014. J Lab Autom. 19: 19-34. PMID: 23975389
  6. Delayed post-operative haemorrhage after carmustine wafer implantation: a case series from two UK centres.  |  Shah, RS., et al. 2014. Br J Neurosurg. 28: 488-94. PMID: 24313309
  7. The combination of carmustine wafers and fotemustine in recurrent glioblastoma patients: a monoinstitutional experience.  |  Lombardi, G., et al. 2014. Biomed Res Int. 2014: 678191. PMID: 24812626
  8. Efficacy and safety of carmustine wafers in the treatment of glioblastoma multiforme: a systematic review.  |  Zhang, YD., et al. 2014. Turk Neurosurg. 24: 639-45. PMID: 25269031
  9. The computational study of the γ-Fe2O3 nanoparticle as Carmustine drug delivery system: DFT approach.  |  Khorram, R., et al. 2019. J Biomol Struct Dyn. 37: 454-464. PMID: 29381124
  10. Protective role of the dried white mulberry extract on the reproductive damage and fertility in rats treated with carmustine.  |  Inanc, ME., et al. 2022. Food Chem Toxicol. 163: 112979. PMID: 35398183
  11. Inhibition of cellular antioxidants: a possible mechanism of toxic cell injury.  |  Puglia, CD. and Powell, SR. 1984. Environ Health Perspect. 57: 307-11. PMID: 6094175
  12. Nitrosoureas: a review of experimental antitumor activity.  |  Schabel, FM. 1976. Cancer Treat Rep. 60: 665-98. PMID: 782694
  13. The mechanism of thioredoxin reductase from human placenta is similar to the mechanisms of lipoamide dehydrogenase and glutathione reductase and is distinct from the mechanism of thioredoxin reductase from Escherichia coli.  |  Arscott, LD., et al. 1997. Proc Natl Acad Sci U S A. 94: 3621-6. PMID: 9108027

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Carmustine, 25 mg

sc-204671
25 mg
$105.00

Carmustine, 25 mg

sc-204671-CW
25 mg
$128.00

Carmustine, 100 mg

sc-204671A
100 mg
$320.00

What is the appearance of the chemical?

Asked by: two2igm05
Thank you for your question. The compound, sc-205616, is provided as a light yellow solid. If you have any further questions or concerns, please feel free to contact our Technical Service department by calling 800-457-3801 option 2, emailing scbt@scbt.com. or using the Live Chat function on our website.
Answered by: Tech Service 8
Date published: 2017-01-19

CAS 154-93-8 产品如何购买?货期大概多长?

Asked by: Krystal
感谢您的提问。关于中国大陆地区的订购事宜,请通过网页上的LiveChat - 中文支持、电话(+86) 021-60936351、或邮箱asia@scbio.cn,联系我们的上海分公司。 Thank you for your inquiry. For purchasing in mainland China, please contact our Shanghai office at (+86) 021-60936351 or asia@scbio.cn, or via LiveChat - Chinese Department on the website.
Answered by: Technical Support
Date published: 2016-12-01
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Rated 5 out of 5 by from Tseng YY; et alTseng YY; et al. (PubMed ID: 26209775) determined that Carmustine, when released with biodegradable drug-eluting nanofibrous membranes, enhances the effectivity of this chemotherapuetic drug. -SCBT Publication Review
Date published: 2015-02-12
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Carmustine is rated 5.0 out of 5 by 1.
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