ChemicalBook > CAS DataBase List > Dexrazoxane

Dexrazoxane

Product Name
Dexrazoxane
CAS No.
24584-09-6
Chemical Name
Dexrazoxane
Synonyms
adr529;cardioxane;DEXRAZOXANE;(S)-ICRF-187;DEXTRAZOXANE;DEXTRORAZOXANE;Dexrazoxane>Right razoxane;(+)-dexrazoxane;Dexrazoxane, >=99%
CBNumber
CB2251448
Molecular Formula
C11H16N4O4
Formula Weight
268.27
MOL File
24584-09-6.mol
More
Less

Dexrazoxane Property

Melting point:
194-196°C
alpha 
D +11.35° (c = 5 in DMF)
Boiling point:
531.5±50.0 °C(Predicted)
Density 
1.333±0.06 g/cm3(Predicted)
storage temp. 
2-8°C
solubility 
DMSO: >20mg/mL
form 
powder
pka
2.1(at 25℃)
color 
white to off-white
Merck 
14,8123
InChIKey
BMKDZUISNHGIBY-ZETCQYMHSA-N
CAS DataBase Reference
24584-09-6(CAS DataBase Reference)
More
Less

Safety

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36
RIDADR 
UN 2811 6.1 / PGIII
WGK Germany 
3
RTECS 
TL6390000
HS Code 
2933.59.9500
Hazardous Substances Data
24584-09-6(Hazardous Substances Data)
More
Less

Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H315Causes skin irritation

H319Causes serious eye irritation

H335May cause respiratory irritation

Precautionary statements

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P264Wash hands thoroughly after handling.

P264Wash skin thouroughly after handling.

P271Use only outdoors or in a well-ventilated area.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P302+P352IF ON SKIN: wash with plenty of soap and water.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

More
Less

N-Bromosuccinimide Price

Sigma-Aldrich
Product number
D1446
Product name
Dexrazoxane
Purity
≥95% (HPLC)
Packaging
5mg
Price
$106
Updated
2024/03/01
Sigma-Aldrich
Product number
05587
Product name
Dexrazoxane
Purity
analytical standard
Packaging
25mg
Price
$94.4
Updated
2024/03/01
TCI Chemical
Product number
D4227
Product name
Dexrazoxane
Purity
>98.0%(T)
Packaging
100mg
Price
$67
Updated
2024/03/01
Cayman Chemical
Product number
14632
Product name
Dexrazoxane
Purity
≥98%
Packaging
5mg
Price
$32
Updated
2024/03/01
Cayman Chemical
Product number
14632
Product name
Dexrazoxane
Purity
≥98%
Packaging
10mg
Price
$48
Updated
2024/03/01
More
Less

Dexrazoxane Chemical Properties,Usage,Production

Description

Dexrazoxane is the dextro-isomer of razoxane approved as a protectant against the cardiotoxicity of doxorubicin in breast cancer patients. This agent does not alter the anticancer effect of doxorubicin. Its mode of action suggests a chelation of free radicals. In mice, dexrazoxane also offers protection against cardiac side effects of epirubicin, but not mitoxantrone.

Originator

Imperial Cancer Research Fund (United Kingdom)

Uses

Dexrazoxane is a cardioprotective compound against anthracyclines. It is highly protective in reducing anthracycline-induced cardiotoxicity and extravasation injury. It functions by inhibiting topoisomerase II without inducing DNA strand breaks. Dexrazoxane is a + enantiomer of razoxane.

Uses

Dexrazoxane has been used in chromatin remodelling experiments.

Uses

Cardioprotectant.

Definition

ChEBI: (+)-dexrazoxane is a razoxane. It has a role as a chelator, an antineoplastic agent, a cardiovascular drug and an immunosuppressive agent.

brand name

Zinecard (Pharmacia & Upjohn);Cardioxane.

General Description

Dexrazoxane is a member of bis(2,6-dioxopiperazines), that functions as a topoisomerase 2 catalytic inhibitor. Dexrazoxane is a free radical scavenger. It might protect the heart from doxorubicin-associated damage. Dexrazoxane acts as a cardiopulmonary protectant, while treating Hodgkin′s disease (HD). It functions as a chelating agent, which limits the formation of anthracycline-iron complexes. It is used to synthesize antimalarial drugs.

Biological Activity

Topoisomerase II inhibitor and intracellular ion chelator. Bridges and stabilizes an interface between two ATPase promoters to inhibit topoisomerase II activity. Cardioprotective when co-administered with doxorubicin; decreases formation of reactive oxygen species (ROS) and activates the PI3K/Akt survival pathway.

Biochem/physiol Actions

Dexrazoxane is a cardioprotective compound against anthracyclines. It functions by inhibiting topoisomerase II without inducing DNA strand breaks. Dexrazoxane is a + enantiomer of razoxane.

Clinical Use

Cardioxane? Prevention of cardiotoxicity in patients receiving doxorubicin or epirubicin for breast cancer Savene? : Treatment of extravasation caused by anthracyclines

Veterinary Drugs and Treatments

Dexrazoxane may be useful to attenuate the cardiotoxic effects of doxorubicin in patients who are showing signs of anthracycline cardiotoxicity, have cardiac disease, or are at maximum cumulative dosages of doxorubicin. It is also used to treat extravasation injuries associated with doxorubicin.
While dexrazoxane has been shown to be cardioprotective when given at dosages of 10 times the doxorubicin dose, there is evidence that it may also partially protect the cancer cells being treated.

Drug interactions

Potentially hazardous interactions with other drugs
Antiepileptics: may reduce absorption of fosphenytoin and phenytoin.
Ciclosporin: increased risk of immunosuppression with risk of lymphoproliferative disease.
Tacrolimus: increased risk of immunosuppression with risk of lymphoproliferative disease.
Vaccines: risk of generalised infections with live vaccines - avoid.

Metabolism

Dexrazoxane is hydrolysed by the enzyme dihydropyrimidine amidohydrolase in the liver and kidney to active metabolites that are capable of binding to metal ions.
It is excreted unchanged via the kidney

Dexrazoxane Preparation Products And Raw materials

Raw materials

Preparation Products

More
Less

Dexrazoxane Suppliers

Pure Chemistry Scientific Inc.
Tel
001-857-928-2050 or 1-888-588-9418
Fax
001-617-206-9595
Email
sales@chemreagents.com
Country
United States
ProdList
10186
Advantage
62
LGM Pharma
Tel
1-(800)-881-8210
Fax
615-250-9817
Email
inquiries@lgmpharma.com
Country
United States
ProdList
2123
Advantage
70
BOC Sciences
Tel
1-631-485-4226; 16314854226
Email
info@bocsci.com
Country
United States
ProdList
14055
Advantage
65
MedChemexpress LLC
Tel
021-58955995
Fax
609-228-5909
Email
sales@medchemexpress.cn
Country
United States
ProdList
4861
Advantage
58
EMMX Biotechnology LLC
Tel
888-539-0666
Fax
888-539-0666
Email
info@emmx.com
Country
United States
ProdList
8447
Advantage
60
BOC Sciences
Tel
16314854226
Email
info@bocsci.com
Country
United States
ProdList
9923
Advantage
65
Musechem
Tel
+1-800-259-7612
Fax
+1-800-259-7612
Email
info@musechem.com
Country
United States
ProdList
4660
Advantage
60
TargetMol Chemicals Inc.
Tel
+1-781-999-5354 +1-00000000000
Email
marketing@targetmol.com
Country
United States
ProdList
32165
Advantage
58
InvivoChem
Tel
+1-708-310-1919 +1-13798911105
Fax
708-557-7486
Email
sales@invivochem.cn
Country
United States
ProdList
6391
Advantage
58
Alchem Pharmtech,Inc.
Tel
8485655694
Email
sales@alchempharmtech.com
Country
United States
ProdList
63687
Advantage
58
Aladdin Scientific
Tel
+1-+1(833)-552-7181
Email
sales@aladdinsci.com
Country
United States
ProdList
57505
Advantage
58
Protheragen-ING
Tel
+16313385890
Email
info@protheragen-ing.com
Country
United States
ProdList
3868
Advantage
58
ApexBio Technology
Tel
--
Fax
--
Email
sales@apexbt.com
Country
United States
ProdList
6251
Advantage
58
Santa Cruz Biotechnology, Inc.
Tel
--
Fax
--
Email
scbt@scbt.com
Country
United States
ProdList
3597
Advantage
60
AlliChem, LLC
Tel
--
Fax
--
Email
sales@allichemllc.com
Country
United States
ProdList
6516
Advantage
60
Cayman Chemical Company
Tel
--
Fax
--
Email
cayman@caymanchem.com
Country
United States
ProdList
6213
Advantage
81
MilliporeSigma (Sigma-Aldrich Corp.)
Tel
--
Fax
--
Email
@sial.com
Country
United States
ProdList
5414
Advantage
58
Byron Chemical Company, Inc
Tel
--
Fax
--
Email
bcc@byronchemical.com
Country
United States
ProdList
88
Advantage
58
Selleck Chemicals LLC
Tel
--
Fax
--
Email
sales@selleckchem.com
Country
United States
ProdList
1848
Advantage
58
Alcami Corporation (formerly Cambridge Major Laboratories Inc.)
Tel
--
Fax
--
Email
info@alcaminow.com
Country
United States
ProdList
3
Advantage
58
TCI America, Inc. (Tokyo Chemical Industry Co., Ltd.)
Tel
--
Fax
--
Email
.Crew@tcichemicals.com
Country
United States
ProdList
3164
Advantage
58
MP Biomedicals, LLC. (Division of Valiant FC Co., Ltd.)
Tel
--
Fax
--
Email
serv@mpbio.com
Country
United States
ProdList
1854
Advantage
58
OChem Incorporation
Tel
--
Fax
--
Email
sales@ocheminc.com
Country
United States
ProdList
6501
Advantage
60
MedChemExpress
Tel
--
Fax
--
Email
sales@medchemexpress.com
Country
United States
ProdList
6398
Advantage
58
ALCAMI WISCONSIN CORP
Tel
--
Fax
--
Email
TALENT.ACQUISITION@ALCAMINOW.COM
Country
United States
ProdList
6
Advantage
58
Combi-Blocks Inc.
Tel
--
Fax
--
Email
sales@combi-blocks.com
Country
United States
ProdList
6618
Advantage
69
Riedel-de Haen AG
Tel
--
Fax
--
Country
United States
ProdList
6773
Advantage
87
TCI America
Tel
--
Fax
--
Email
sales@tciamerica.com
Country
United States
ProdList
6909
Advantage
75
Matrix Scientific
Tel
--
Fax
--
Email
sales@matrixscientific.com
Country
United States
ProdList
6632
Advantage
80
Waterstone Technology, LLC
Tel
--
Fax
--
Email
sales@waterstonetech.com
Country
United States
ProdList
6786
Advantage
30
Synthland Hong Kong Limited
Tel
--
Fax
--
Email
info@synthlandpharm.com
Country
United States
ProdList
45
Advantage
50
LKT Laboratories, Inc.
Tel
--
Fax
--
Email
info@lktlabs.com
Country
United States
ProdList
2164
Advantage
64
AK Scientific, Inc.
Tel
--
Fax
--
Email
sales@aksci.com
Country
United States
ProdList
6347
Advantage
65
2A PharmaChem USA
Tel
--
Fax
--
Email
sales@2apharmachem.com
Country
United States
ProdList
6137
Advantage
39
3B Scientific Corporation
Tel
--
Fax
--
Email
sales@3bsc.com
Country
United States
ProdList
6718
Advantage
47
APAC Pharmaceutical, LLC
Tel
--
Fax
--
Email
sales@apacpharma.com
Country
United States
ProdList
6322
Advantage
38
ChemPacific Corporation
Tel
--
Fax
--
Email
sales@chempacific.com
Country
United States
ProdList
6891
Advantage
51
More
Less

View Lastest Price from Dexrazoxane manufacturers

hebei hongtan Biotechnology Co., Ltd
Product
Dexrazoxane 24584-09-6
Price
US $60.00/kg
Min. Order
1kg
Purity
99%
Supply Ability
1000
Release date
2024-03-25
WUHAN FORTUNA CHEMICAL CO., LTD
Product
Dexrazoxane 24584-09-6
Price
US $0.00/Kg/Bag
Min. Order
1g
Purity
98%-102%
Supply Ability
10KGS
Release date
2021-07-16
Hangzhou Hyper Chemicals Limited
Product
Dexrazoxane 24584-09-6
Price
US $0.00-0.00/KG
Min. Order
1KG
Purity
99%, USP
Supply Ability
5,000KG
Release date
2024-08-30

24584-09-6, DexrazoxaneRelated Search:


  • DEXRAZOXANE
  • (s)-4,4'-(1-methyl-1,2-ethanediyl)bis-2,6-piperazinedione
  • 4’-(1-methyl-1,2-ethanediyl)bis-6-piperazinedion(+)-4
  • 4’-propylenedi-6-piperazinedion(+)-4
  • adr529
  • cardioxane
  • DEXTRAZOXANE
  • DEXTRORAZOXANE
  • (S)-1,2-Bis(3,5-dioxo-1-piperazinyl)propane
  • (S)-ICRF-187
  • [S,(+)]-4,4'-Propylenebis(2,6-piperazinedione)
  • 4,4'-[(S)-1-Methyl-1,2-ethanediyl]bis(2,6-piperazinedione)
  • 4-[(2S)-2-(3,5-Dioxopiperazin-1-yl)propyl]piperazine-2,6-dionehydrochloride
  • 4-[(2S)-2-(3,5-dioxopiperazin-1-yl)propyl]piperazine-2,6-dione
  • (S)-4,4'-(Propane-1,2-diyl)bis(piperazine-2,6-dione)
  • Dexrazoxane ((S)-Razoxane)
  • 2,6-Piperazinedione,4,4'-[(1S)-1-Methyl-1,2-ethanediyl]bis-
  • (+)-(S)-4,4′-Propylenedi-2,6-piperazinedione
  • (S)-(+)-1,2-Bis(3,5-dioxopiperazin-1-yl)propane
  • Dexrazoxane (S)-4,4'-(1-Methyl-1,2-ethanediyl)bis-2,6-piperazinedione)
  • Dexrazoxane, >=99%
  • Ca rdioxane、Dextrazoxane、Eucardion、Zinecard
  • ICRF-187;NSC-169780
  • Dexrazoxane (ICRF-187
  • Dexrazoxane&gt
  • (+)-dexrazoxane
  • Dexrazoxane Impurity
  • Dexrazoxane (NSC-169780)
  • Dextrozosan. - Dextropropimide
  • Right razoxane
  • Dexrazoxane 24584-09-6
  • 4,4'-[(1S)-1-Methyl-1,2-ethanediyl]bis-2,6-piperazinedione
  • 2,6-Piperazinedione, 4,4'-[(1S)-1-methyl-1,2-ethanediyl]bis-
  • 24584-09-6
  • C11H16N4O4
  • API
  • Chelating Agent
  • 24584-09-6