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Merck

C1768

Sigma-Aldrich

Cytarabine

≥90% (HPLC), crystalline, DNA replication inhibitor

Synonym(e):

(β-D-Arabinofuranosyl)-cytosin, Ara-C, Arabinocytidin, Arabinosylcytosin, Cytarabin, Cytosinarabinosid

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100 MG
CHF 78.70
500 MG
CHF 163.00
1 G
CHF 322.00
5 G
CHF 900.00

CHF 78.70


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100 MG
CHF 78.70
500 MG
CHF 163.00
1 G
CHF 322.00
5 G
CHF 900.00

About This Item

Empirische Formel (Hill-System):
C9H13N3O5
CAS-Nummer:
Molekulargewicht:
243.22
Beilstein:
89175
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
12352200
PubChem Substanz-ID:
NACRES:
NA.77

CHF 78.70


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Produktbezeichnung

Cytosin β-D-Arabinofuranosid, crystalline, ≥90% (HPLC)

Qualitätsniveau

Assay

≥90% (HPLC)

Form

crystalline

Lagertemp.

2-8°C

SMILES String

NC1=NC(=O)N(C=C1)[C@@H]2O[C@H](CO)[C@@H](O)[C@@H]2O

InChI

1S/C9H13N3O5/c10-5-1-2-12(9(16)11-5)8-7(15)6(14)4(3-13)17-8/h1-2,4,6-8,13-15H,3H2,(H2,10,11,16)/t4-,6-,7+,8-/m1/s1

InChIKey

UHDGCWIWMRVCDJ-CCXZUQQUSA-N

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Verwandte Kategorien

Biochem./physiol. Wirkung

Ara-C wird in DNA eingebaut und hemmt die DNA-Replikation durch Bildung von Spaltkomplexen mit Topoisomerase I, was zu einer Fragmentierung der DNA führt; die RNA-Synthese wird nicht gehemmt. Anti-Leukämiemittel.

Leistungsmerkmale und Vorteile

Diese Verbindung ist ein wichtiges Produkt für die Forschung im Bereich der Apoptose. Weitere empfohlene Apoptoseprodukte finden Sie hier. Weitere Informationen über bioaktive kleine Moleküle für andere Forschungsbereiche finden Sie unter sigma.com/discover-bsm.

Piktogramme

Health hazardExclamation mark

Signalwort

Warning

H-Sätze

Gefahreneinstufungen

Repr. 2 - Skin Sens. 1

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Persönliche Schutzausrüstung

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges


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In der Dokumentenbibliothek finden Sie die Dokumentation zu den Produkten, die Sie kürzlich erworben haben.

Die Dokumentenbibliothek aufrufen

Sonia G Das et al.
Journal of medicinal chemistry, 54(16), 5937-5948 (2011-07-26)
Multidrug resistance (MDR) in cancer is a phenomenon in which administration of a single chemotherapeutic agent causes cross-resistance of cancer cells to a variety of therapies even with different mechanisms of action. Development of MDR against standard therapies is a
Hamed I Ali et al.
Bioorganic & medicinal chemistry, 15(1), 242-256 (2006-10-20)
Novel 2-deoxo-2-phenyl-5-deazaflavins and 2-deoxo-2-phenylflavin-5-oxides were prepared as a new class of antitumor agents and showed significant antitumor activities against NCI-H 460, HCT 116, A 431, CCRF-HSB-2, andKB cell lines. In vivo investigation, 2-deoxo-10-methyl-2-phenyl-5-deazaflavin exhibited the effective antitumor activity against A
Bob Löwenberg
Blood, 121(1), 26-28 (2013-01-05)
High-dose cytarabine applied during remission induction or as consolidation after attainment of a complete remission has become an established element in the treatment of adults with acute myeloid leukemia. Recent evidence has challenged the need for these exceptionally high-dose levels
Jorge Cortes et al.
The Lancet. Oncology, 14(4), 354-362 (2013-03-05)
Tosedostat is a novel oral aminopeptidase inhibitor with clinical activity in a previous phase 1-2 study in elderly patients with relapsed or refractory acute myeloid leukaemia (AML). We aimed to compare two dosing regimens of tosedostat. In this randomised phase
Alberto Diez-Torrubia et al.
Journal of medicinal chemistry, 53(2), 559-572 (2009-12-17)
Here we explore the applicability of the dipeptidyl peptidase IV (DPPIV/CD26) based prodrug approach to a variety of amine-containing drugs. Efficient procedures have been developed for the synthesis of dipeptide and tetrapeptide amide prodrugs including N-acylation protocols of the exocyclic

Artikel

DNA damage and repair mechanism is vital for maintaining DNA integrity. Damage to cellular DNA is involved in mutagenesis, the development of cancer among others.

Cell cycle phases (G1, S, G2, M) regulate cell growth, DNA replication, and division in proliferating cells.

Apoptosis regulation involves multiple pathways and molecules for cellular homeostasis.

Questions

1–3 of 3 Questions  
  1. How long could a solution of 2uM be stable at -80C? Would this storage help the aliquots last longer than a year at -20C?

    1 answer
    1. The stability of this product in solution for extended periods has not been determined. Stock solutions stored in aliquots at -70°C are stable up to 6 months. Stock solutions may also be stored at -20°C, however no time frame has been established.

      Helpful?

  2. Hello, does the freeze-thaw cycle affect the potency or stability of cytarabine?

    1 answer
    1. The freeze-thaw stability of this material in solution has not been determined. However, Cold Spring Harbor Protocols suggests solutions are stable for several weeks when refrigerated. For long term storage, store solutions in working aliquots at −20°C . Please see the link below to review this information:
      https://cshprotocols.cshlp.org/content/2008/12/pdb.rec11555.full?text_only=true

      Helpful?

  3. Does cytoine beta d arabinofuranoside (Arac) solution filterable by .22um filter ,, is it good idea to filter ara c

    1 answer
    1. This product is soluble in water at 50 mg/mL and may be filter sterilized. It is recommended to use a low protein binding filter membrane, such as PES, to prevent product retention in the filter. Solution stability has not been determined, however, Cold Spring Harbor protocols suggest that the filtered stock solution may be stored refrigerated or frozen.

      See the link below to review:
      https://cshprotocols.cshlp.org/content/2008/12/pdb.rec11555.full?text_only=true

      Helpful?

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