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C0768

Cyclophosphamide monohydrate

97.0-103.0% (HPLC), Alkylating agent, powder

Sinonimo/i:

2-[Bis(2-chloroethyl)amino]tetrahydro-2H-1,3,2-oxazaphosphorine 2-oxide, Cytoxan

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1 g
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CHF 119.00
5 g
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CHF 240.00
10 g
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CHF 372.00
25 g
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CHF 837.00

Informazioni su questo articolo

Formula empirica (notazione di Hill):
C7H15Cl2N2O2P · H2O
Numero CAS:
Peso molecolare:
279.10
NACRES:
NA.77
PubChem Substance ID:
UNSPSC Code:
51112507
EC Number:
200-015-4
MDL number:
Beilstein/REAXYS Number:
4678992
Assay:
97.0-103.0% (HPLC)
Form:
powder
Quality level:

CHF 119.00


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Nome del prodotto

Cyclophosphamide monohydrate, bulk package

Quality Level

assay

97.0-103.0% (HPLC)

form

powder

mp

49-51 °C (lit.)

storage temp.

2-8°C

SMILES string

[H]O[H].ClCCN(CCCl)P1(=O)NCCCO1

InChI

1S/C7H15Cl2N2O2P.H2O/c8-2-5-11(6-3-9)14(12)10-4-1-7-13-14;/h1-7H2,(H,10,12);1H2

InChI key

PWOQRKCAHTVFLB-UHFFFAOYSA-N

Gene Information

General description

Cyclophosphamide (CYC) is a cytotoxic alkylating agent. It is activated by the cytochrome P-450 enzyme system in the liver. It has immunomodulatory functionality and inhibits humoral and cellular immunity.Cyclophosphamide exhibits anti-cancer and immunosuppressant activities.[1] In the body, cyclophosphamide is converted by the liver to an active alkylating 4-hydroxycyclophosphamide metabolite, thereby showing its anti-neoplastic effects.

Application

Cyclophosphamide monohydrate has been used:
  • to test its antitumor effect on TC-1 tumor cells
  • as a component of multidrug solution for isolation of resistant human burkitt lymphoma cell line
  • in testing antitumor immunity in mouse tumor cell lines

Biochem/physiol Actions

Cyclophosphamide is a cytotoxic nitrogen mustard derivative widely used in cancer chemotherapy. It cross-links DNA, causes strand breakage, and induces mutations. Its clinical activity is associated with a decrease in aldehyde dehydrogenase 1 (ALDH1) activity.
Cytotoxic nitrogen mustard derivative widely used in cancer chemotherapy. It cross-links DNA, causes strand breakage, and induces mutations.

Features and Benefits

This compound is a featured product for Apoptosis research. Click here to discover more featured Apoptosis products. Learn more about bioactive small molecules for other areas of research at sigma.com/discover-bsm.

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Questo articolo
239785C739793813
assay

97.0-103.0% (HPLC)

assay

≥98% (HPLC)

assay

97.0-103.0% (HPLC)

assay

≥98.0% (HPLC)

form

powder

form

solid

form

powder

form

-

Quality Level

200

Quality Level

100

Quality Level

100

Quality Level

100

storage temp.

2-8°C

storage temp.

2-8°C

storage temp.

2-8°C

storage temp.

2-8°C

Gene Information

human ... ALDH1A1(216), ALDH1B1(219)

Gene Information

-

Gene Information

-

Gene Information

-

mp

49-51 °C (lit.)

mp

-

mp

49-51 °C (lit.)

mp

47-52 °C, 49-51 °C (lit.)


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pictograms

Skull and crossbonesHealth hazard

signalword

Danger

Hazard Classifications

Acute Tox. 3 Oral - Carc. 1B - Muta. 1B - Repr. 1A

Classe di stoccaggio

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

wgk

WGK 3

ppe

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



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Cyclophosphamide pharmacokinetics and dose requirements in patients with renal insufficiency
Haubitz M, et al.
Kidney International, 61(4), 1495-1501 (2002)
J Tammam et al.
British journal of pharmacology, 158(5), 1183-1195 (2009-09-25)
gamma-Secretase inhibitors (GSIs) block NOTCH receptor cleavage and pathway activation and have been under clinical evaluation for the treatment of malignancies such as T-cell acute lymphoblastic leukaemia (T-ALL). The ability of GSIs to decrease T-ALL cell viability in vitro is
Immunosuppressive effect of cyclophosphamide on white blood cells and lymphocyte subpopulations from peripheral blood of Balb/c mice
Huyan XH, et al.
International Immunopharmacology, 11(9), 1293-1297 (2011)



Numero articolo commerciale globale

SKUGTIN
C0768-5G04061835515851
C0768-1G04061835506088
C0768-10G04061833452059
C0768-25G04061833023754

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