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D8809

Daunorubicin -hydrochlorid

meets USP testing specifications

Synonym(e):

Daunomycin -hydrochlorid

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Über diesen Artikel

Empirische Formel (Hill-System):
C27H29NO10 · HCl
CAS-Nummer:
Molekulargewicht:
563.98
UNSPSC Code:
41116107
NACRES:
NA.21
PubChem Substance ID:
EC Number:
245-723-4
Beilstein/REAXYS Number:
4229221
MDL number:
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Quality Level

agency

USP/NF, meets USP testing specifications

form

solid

antibiotic activity spectrum

neoplastics

mode of action

DNA synthesis | interferes

storage temp.

2-8°C

SMILES string

Cl.COc1cccc2C(=O)c3c(O)c4C[C@](O)(C[C@H](O[C@H]5C[C@H](N)[C@H](O)[C@H](C)O5)c4c(O)c3C(=O)c12)C(C)=O

InChI

1S/C27H29NO10.ClH/c1-10-22(30)14(28)7-17(37-10)38-16-9-27(35,11(2)29)8-13-19(16)26(34)21-20(24(13)32)23(31)12-5-4-6-15(36-3)18(12)25(21)33;/h4-6,10,14,16-17,22,30,32,34-35H,7-9,28H2,1-3H3;1H/t10-,14-,16-,17-,22+,27-;/m0./s1

InChI key

GUGHGUXZJWAIAS-QQYBVWGSSA-N

Gene Information

human ... TOP2A(7153)

Biochem/physiol Actions

Wirksames Antikrebsmittel. Hemmt die DNA- und RNA-Synthese als sequenzspezifisches ds-DNA interkalierendes Mittel. Eigenschaften
Naturally fluorescent anthracycline antibiotic, anticancer drug. Substrate for Pgp, MRP-1 and BCRP. Fluorescent property has been exploited for the measurement of drug efflux pump activities as well as resolving the important question of intracellular localization of various multidrug resistance proteins and the role of subcellular organelles (golgi and lysosome) in the sequestration of drugs and its implication in drug resistant phenotypes. Daunorubicin is sequestered into lysosomes according to a pH partitioning type mechanism.[1][2] Strong inhibitor of DNA and RNA synthesis.

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Dieser Artikel
1164700D012500030450
antibiotic activity spectrum

neoplastics

antibiotic activity spectrum

-

antibiotic activity spectrum

-

antibiotic activity spectrum

neoplastics

mode of action

DNA synthesis | interferes

mode of action

-

mode of action

-

mode of action

DNA synthesis | interferes

Quality Level

200

Quality Level

-

Quality Level

-

Quality Level

200

form

solid

form

-

form

-

form

powder

storage temp.

2-8°C

storage temp.

−20°C

storage temp.

-

storage temp.

2-8°C

Gene Information

human ... TOP2A(7153)

Gene Information

human ... TOP2A(7153)

Gene Information

human ... TOP2A(7153)

Gene Information

human ... TOP2A(7153)


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pictograms

Skull and crossbonesHealth hazard

signalword

Danger

Hazard Classifications

Acute Tox. 3 Oral - Carc. 2 - Muta. 2 - Repr. 1B

Lagerklasse

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

ppe

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



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Devika Prasanth et al.
Life (Basel, Switzerland), 10(9) (2020-08-28)
Microgravity or the condition of apparent weightlessness causes bone, muscular and immune system dysfunctions in astronauts following spaceflights. These organ and system-level dysfunctions correlate with changes induced at the single cell level both by simulated microgravity on earth as well
E J Wang et al.
Drug metabolism and disposition: the biological fate of chemicals, 28(5), 522-528 (2000-04-20)
P-glycoprotein (Pgp)-mediated drug efflux is a major factor contributing to the variance of absorption and distribution of many drugs. A simple and reliable in vitro method to identify inhibitors of Pgp helps to prevent the potential of drug interactions. Using
Yuping Gong et al.
The Journal of biological chemistry, 278(50), 50234-50239 (2003-10-03)
The sequestration of drugs away from cellular target sites into cytoplasmic organelles of multidrug-resistant (MDR) cancer cells has been recently shown to be a cause for ineffective drug therapy. This process is poorly understood despite the fact that it has



Global Trade Item Number

SKUGTIN
D8809-50MG04061834374190
D8809-1MG04061834374183
D8809-10MG04061833589977

Questions

1–5 of 5 Questions  
  1. What factors affect the stability of Product No. D8809, Daunorubicin hydrochloride, in solution?

    1 answer
    1. Per Martindale The Extra Pharmacopoeia, 31st edition, p. 565-3 (1996), stability in solution appeared to be partly related to pH.  Daunorubicin was more stable as the pH of the mixture became more acidic, with the best stability in glucose injection solution (5%) with a pH of 4.5  Although daunorubicin solutions are degraded by light, the effect is reported not to be significant at concentrations of 500 ug/mL or above.  However, below this concentration, precautions should be taken to protect solutions from light, and storage should be in polyethylene or polypropylene containers to minimize adsorptive losses.

      Helpful?

  2. Does the assay information on the certificate of analysis for Product No. D8809, Daunorubicin hydrochloride, pertain to a "dry" or "as is" basis?

    1 answer
    1. The assay information on the certificate of analysis is for the product "as is".

      Helpful?

  3. Does Product No. D8809, Daunorubicin hydrochloride, have an expiration date?

    1 answer
    1. Yes, each lot of this product will have an expiration date, and this date (month and year) can be found on the certificate of analysis for the lot.

      Helpful?

  4. What is the Department of Transportation shipping information for this product?

    1 answer
    1. Transportation information can be found in Section 14 of the product's (M)SDS.To access the shipping information for this material, use the link on the product detail page for the product.

      Helpful?

  5. What is this compound soluble in?

    1 answer
    1. Per Martindale The Extra Pharmacopoeia, 31st edition, p. 565-3 (1996), this compound is freely soluble in water and methyl alcohol.  It is slightly soluble in alcohol, very slightly soluble in chloroform, and practically insoluble in acetone.

      Helpful?

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