Overview Indications Mechanism of action Administration and formulation Pharmacokinetics Side effects References
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Doxorubicin hydrochloride

Overview Indications Mechanism of action Administration and formulation Pharmacokinetics Side effects References
Product Name
Doxorubicin hydrochloride
CAS No.
25316-40-9
Chemical Name
Doxorubicin hydrochloride
Synonyms
DOX;ADR;Caely;fi6804;CAELYX;FI 106;DOX HCl;Lipodox;ADRIACIN;Ardriamycin
CBNumber
CB0110633
Molecular Formula
C27H30ClNO11
Formula Weight
579.98
MOL File
25316-40-9.mol
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Doxorubicin hydrochloride Property

Melting point:
216 °C (dec.)(lit.)
alpha 
D20 +248±2° (c = 0.1 in methanol)
storage temp. 
2-8°C
solubility 
H2O: 10 mg/mL, clear, red-orange
pka
pKa 8.25±0.60 (Uncertain);8.43±0.70 (Uncertain);11.9±0.4 (Uncertain);12.95±0.1 (Uncertain);13.8±0.70 (Uncertain)
form 
solid
color 
orange to dark red
Water Solubility 
Soluble in water.
λmax
497nm(H2O)(lit.)
Merck 
14,3439
BRN 
4229251
InChIKey
MWWSFMDVAYGXBV-RUELKSSGSA-N
CAS DataBase Reference
25316-40-9(CAS DataBase Reference)
EPA Substance Registry System
5,12-Naphthacenedione, 10-[(3-amino-2,3,6-trideoxy-. alpha.-L-lyxo-hexopyranosyl) oxy]-7,8,9,10-tetrahydro- 6,8,11-trihydroxy-8-(hydroxyacetyl)- 1-methoxy-, hydrochloride, (8S,10S)-(25316-40-9)
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Safety

Hazard Codes 
T,T+,Xi
Risk Statements 
45-22-40-26/27/28-36/38
Safety Statements 
53-45-36/37/39-22-7/9
WGK Germany 
3
RTECS 
QI9295900
10-21
HS Code 
29419090
Toxicity
LD50 i.v. in mice: 21.1 mg/kg (Bertazzoli, 1970)
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Danger
Hazard statements

H302Harmful if swallowed

H315Causes skin irritation

H319Causes serious eye irritation

H350May cause cancer

H351Suspected of causing cancer

H361Suspected of damaging fertility or the unborn child

H373May cause damage to organs through prolonged or repeated exposure

Precautionary statements

P201Obtain special instructions before use.

P202Do not handle until all safety precautions have been read and understood.

P260Do not breathe dust/fume/gas/mist/vapours/spray.

P264Wash hands thoroughly after handling.

P264Wash skin thouroughly after handling.

P270Do not eat, drink or smoke when using this product.

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

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

P308+P313IF exposed or concerned: Get medical advice/attention.

P405Store locked up.

P501Dispose of contents/container to..…

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N-Bromosuccinimide Price

Sigma-Aldrich
Product number
44583
Product name
Doxorubicin hydrochloride
Purity
suitable for fluorescence, 98.0-102.0% (HPLC)
Packaging
1mg
Price
$46.9
Updated
2018/11/20
Sigma-Aldrich
Product number
1225703
Product name
Doxorubicin hydrochloride
Purity
United States Pharmacopeia (USP) Reference Standard
Packaging
50mg
Price
$1080.45
Updated
2018/11/20
TCI Chemical
Product number
D4193
Product name
Doxorubicin Hydrochloride
Purity
>95.0%(HPLC)
Packaging
25mg
Price
$38
Updated
2018/11/22
TCI Chemical
Product number
D4193
Product name
Doxorubicin Hydrochloride
Purity
>95.0%(HPLC)
Packaging
100mg
Price
$116
Updated
2018/11/22
Alfa Aesar
Product number
J64000
Product name
Doxorubicin hydrochloride
Packaging
10mg
Price
$170
Updated
2018/11/13
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Doxorubicin hydrochloride Chemical Properties,Usage,Production

Overview

Doxorubicin (DXR) is a clinically important cancer chemotherapeutic agent and, in spite of undesirable acute and long-term toxic effects, DXR remains one of the most widely used antitumor drugs because of its broad spectrum of activity[1]. DXR was first isolated in 1969[1] from Streptomyces peucetius subsp caesius ATCC 27952, a higher DXR-producing mutant strain derived from the wild-type S. peucetius ATCC 29050 strain, and is formed by C-14 hydroxylation of its immediate precursor, DNR. Although a number of organisms (including the 29050 strain) are known to produce DNR [2], S. peucetius subsp caesius is the only organism reported to produce DXR. The current production of DXR is over 225 kilograms annually due to its wide use and the fact that it is the starting point for the synthesis of numerous analogs and derivatives aimed at improving clinical cancer treatment[1]. Although DXR was discovered as a microbial metabolite, it is produced commercially by semi-synthesis from the more abundant DNR instead of by fermentation. High-DNR producing strains are available worldwide yet apparently lack the ability to make useful amounts of DXR or the DXR produced cannot easily be separated from the DNR that also is present. Consequently, the development of improved strains for DXR production is a beneficial goal since this drug is an expensive product.

Figure 1 the chemical structure of DXR

Much effort has been devoted to unraveling the mechanism of antitumor action of doxorubicin. Currently the belief is widespread that free radical formation is critically involved in the mechanism of cytotoxicity of doxorubicin against tumor cells. However, most of the evidence favoring a free radical-dependent model has been obtained by studying subcellular fractions, often in combination with extremely high concentrations of doxorubicin that are not encountered in clinical practice.

Indications

Doxorubicin is a potent antitumour agent active against a wide spectrum of malignancies, including leukaemias, sarcomas, breast cancer, small cell lung cancer and ovarian cancer. Doxorubicin is used to produce regression in disseminated neoplastic conditions like acute lymphoblastic leukemia, acute myeloblastic leukemia, Wilms’ tumor, neuroblastoma, soft tissue and bone sarcomas, breast carcinoma, ovarian carcinoma, transitional cell bladder carcinoma, thyroid carcinoma, gastric carcinoma, Hodgkin's disease, malignant lymphoma and bronchogenic carcinoma in which the small cell histologic type is the most responsive compared to other cell types. Doxorubicin is also indicated for use as a component of adjuvant therapy in women with evidence of axillary lymph node involvement following resection of primary breast cancer. Doxorubicin does not playa crucial role in the treatment of tumours that can be cured with chemotherapy, such as testicular carcinoma, nephroblastoma, Burkitt's tumour and choriocarcinoma[3]. Like most other cytostatic agents, doxorubicin is not effective in the most frequently occurring malignancies such as colorectal cancer and non-small cell lung cancer.

Mechanism of action

Doxorubicin has antimitotic and cytotoxic activity through a number of proposed mechanisms of action, however, remaining not fully understood: Data pointing to the role of free radicals, and to damage of mitochondria and membranes, have modified the original hypothesis that DNA-intercalation was the sole cytotoxic mechanism. Meanwhile, the focus on plasma pharmacokinetics has been shifted towards pharmacodynamic studies, with emphasis on cellular doxorubicin concentrations in haematopoietic tissues[4], in solid tumours[5], and in cell constituents. Doxorubicin forms complexes with DNA by intercalation between base pairs. In addition, doxorubicin-iron complexes bind tightly to DNA[6]. However, contrary to intercalated doxorubicin, the doxorubicin-iron complex preserves its ability to catalyze the formation of oxygen free radicals in the presence of double-stranded DNA[6]. Thus, the doxorubicin-iron complex-driven hydroxyl radical formation can proceed in close proximity to DNA and has therefore the potential to damage DNA efficiently, especially since DNA seems to catalyze hydroxyl radical formation by this complex[7]. Hydroxyl radicals are probably involved in damaging of DNA since the generation of hydroxyl radicals by the Dox-iron complex correlates with its ability to cleave DNA[7] and also since catalase, iron chelates and hydroxyl radical scavengers are protective in this system[6]. Relatively high concentrations of hydroxyl radical scavengers were required for protection, indicating that these radicals were indeed generated in a site-specific way.
Moreover, it inhibits topoisomerase II activity by stabilizing the DNA-topoisomerase II complex, preventing the religation portion of the ligation-religation reaction that topoisomerase II catalyzes. Topoisomerase II causes transient double-strand breaks during the twisting of 2 double-stranded DNA helices. Singleand double-stranded DNA breaks have been documented after in vivo and in vitro treatment with doxorubicin of P388 leukaemia cells in mice[8].
Special reference must be made to observations that interference with the cell membrane alone may lead to cell death [9]. Doxorubicin binding to membranes, and particularly its covalent binding to cardiolipin, a phospholipid with 2 negatively charged phosphate head groups, has received much attention[10]. Cardiolipin is found in the inner leaflet of the mitochondrial membrane and is closely associated with electron transport mechanisms. Goormaghtigh et al. (1983) [10] have shown that doxorubicin bound to cardiolipin undergoes redox cycling, producing covalent binding of doxorubicin to cardiolipin in mitochondrial membranes. The hydrophobic nature of the chromophore of anthracyclines allows partitioning into the lipid phase, resulting in changed fluidity of the membrane. Diminished membrane fluidity is related to doxorubicin resistance. A detailed study of the mechanisms involved in doxorubicin-induced changes in membrane structure and function has not been undertaken. However, doxorubicin binds to the epidermal growth factor receptor at clinically relevant drug concentrations, and alters its function.

Administration and formulation

Doxorubicin is available as a dry powder; reconstituted in water, it is most stable at a mildly acidic pH of 4, and unstable at a very acidic or basic pH[11]. When diluted in 0.9% sodium chloride or dextrose 5%, less than 5% decomposition occurred over 7 to 30 days[12]. It is stable in light at room temperature for at least 24 hours [12], although stability may be shorter in plasma and culture media[11].
Doxorubicin has been administered intravenously, intra-arterially, intraperitoneally, intrapleurally and intravesically. A bioavailability of 5% prohibits oral administration[13]. Subcutaneous, intramuscular and intrathecal application cannot be used, as severe tissue necrosis results, as in extravasation.

Pharmacokinetics

Absorption
An intravenous bolus injection of doxorubicin produces high plasma concentrations, which fall quickly due to rapid and extensive distribution into tissues. 50 to 85% of plasma doxorubicin is bound to protein[13], independent of the absolute drug concentration in plasma, leaving 15 to 50% of the total doxorubicin and doxorubicinol as free drug. After repeated injections no accumulation in plasma occurs. Apparent volumes of distribution are in the range of 20 to 30 L/kg (1400 to 3000L)[14].
Doxorubicin does not cross the blood-brain barrier and is therefore inactive against tumours in the central nervous system[15]. Some transplacental passage has been observed, although healthy children have been born after pregnancies during which doxorubicin was administered from the first to the third trimester[16]. Negligible doxorubicin concentrations have been found in breast milk. Salivary doxorubicin concentrations are 6 to 26% of plasma concentrations during the first 75 minutes after administration[17].

Metabolism
Doxorubicin is rapidly metabolized into the hydrophilic 13-hydoxy1 metabolite, doxorubicinol, and the poorly water-soluble aglycones, doxorubicinone and 7-deoxydoxorubicinone. Like doxorubicin, doxorubicinol is cytotoxic, but doxorubicinone is not[18]. Metabolism to doxorubicino1 occurs by cytoplasmatic NADPH-dependent aldoketoreductases, present in all cells, but particularly in red cells, and liver and kidney cells[18]. The non-cytotoxic aglycones are formed by an NADPH-dependent, cytochrome reductase-mediated cleavage of the amino sugar moiety in microsomes. This enzymatic reduction of doxorubicin is of paramount importance, as it finally produces the OH•-radicals, which cause extensive cell damage and cell death[19].

Elimination
Doxorubicin and its catabolites are primarily excreted in the bile[20]. Over 50% is eliminated during the first transit through the liver. Cumulative faecal excretion over 7 days has been estimated at 25 to 45%[21]; no evidence for enterohepatic recirculation has been observed. Although patients often notice a reddish coloration of the urine during the first hours to days after doxorubicin administration, only 0.7 to 23% (on average, approximately 5%) of a dose has been recovered in the urine[20, 21], of which approximately two-thirds is unaltered drug. Nevertheless, doxorubicin-induced nephrotoxicity has been noted only in mice, rats, rabbits and dogs, and not in humans. The reason for this interspecies difference has not been explained, although stimulated lipid peroxidation may play a role[22]. The doxorubicin plasma concentration-time curve can be best described by a biexponentia1 model, which is characterized by a distribution half-life of less than 5 to 10 minutes, and a terminal phase elimination half-life of 30 ± 8 hours[14]. A triphasic curve with half-lives of 12 ± 8 minutes, 3.3 ± 2.2 hours and 30 ± 14 hours has also been proposed[23].

Side effects

Doxorubicin is a carcinogenic and mutagenic substance. Phlebitis is frequently observed after long-term intravenous infusion[24]. Paravasal leakage causes severe necrosis of skin and adjacent tissues, the extent of which depends on the degree of extravasation[25]. An appropriate antidote is not available. A number of agents injected locally may even worsen the necrosis; however, ice packs and 48 hours' rest may be beneficial[25]. Acute doxorubicin toxicity consists of gastrointestinal complaints and cardiac arrhythmias. Nausea and vomiting occur within 4 to 8 hours of doxorubicin administration and can only be partially controlled by antiemetic drugs. Arrhythmias and electrocardiographic changes are transient. Anaphylactoid and hypersensitivity reactions ('flare') may occur during injection, thus mimicking extravasation, but discontinuation of therapy is not necessary[26]. In long term, infusion the occurrence of acute side effects is almost completely abolished. Repeated administrations of doxorubicin bolus injections, and the resultant high doxorubicin plasma concentrations, have been associated with an increased risk of acute and late-onset cardiotoxicity.
Delayed toxicity consists mainly of myelosuppression, alopecia and cardiomyopathy. At approximately 16 days after a single dose of doxorubicin the white blood cell and platelet counts reach their lowest point. Myelosuppression and alopecia are dose related, but independent of the mode of administration (i.e. peak plasma concentration). The onset of myelosuppression occurs after 7 to 10 days, and recovery at 19 to 24 days after doxorubicin administration. This side effect, although reversible, is dose limiting. Hair loss starts approximately 3 weeks after the first administration of doxorubicin; however, hair growth resumes a few weeks after the last therapy[26]. Local application of ice-packs to prevent hair loss have been of limited value. Mucositis and/or diarrhoea are noticed especially during long-term infusion regimens[24].

References

  1. Arcamone F, et al 1998. Pharmacol Ther 76: 117–124.
  2. Grein A. 1987. Adv Appl Microbiol 32: 203–214
  3. Zubrod CG. Historic milestones in curative chemotherapy. Seminars in Oncology 6: 490-505, 1979
  4. Speth PAJ, et al Clinical Pharmacology and Therapeutics 41: 661-665, 1987
  5. Cummings J, et al Cancer Chemotherapy and Pharmacology 17: 80-84, 1986
  6. ELIOT, H., et al (1984) Biochemistry 23: 928-936.
  7. MUINDI, J. R. F., et al FEBS Lett. 172: 226-230.
  8. Russo P, et al Anticancer Research 6: 1297-1304, 1986
  9. Tritton TR, et al Science 217: 248-250, 1982
  10. Goormaghtigh E, et al Biochemical Pharmacology 32: 889-893, 1983
  11. Bouma J, et al Pharmaceutisch Weekblad, Scientific Edition 8: 109-133, 1986
  12. Benvenuto JA, et al Cancer chemotherapy by infusion, pp. 100-113, Precept Press, Chicago, 1987
  13. Harris PA, et al Cancer Chemotherapy Reports 59: 819-825, 1975
  14. Greene RF, et al Cancer Research 43: 3417-3421, 1983
  15. Mooney C, et al European Journal of Cancer and Oinical Oncology 19: 1037-1038, 1983
  16. Fassas A, et al Nouvelle Revue Fran~ise Hematologique 26: 19-24, 1984
  17. Celio LA, et al European Journal of Clinical Pharmacology 24: 261-266, 1983
  18. Bachur NR, et al Journal of Medicinal Chemistry 19: 651-654, 1976
  19. Myers CE, et al In Lawn (Ed.) Anthracyclines in press, 1988
  20. Takanashi S, et al Drug Metabolism and Disposition 4: 79-87, 1976
  21. DiFronzo G, et al Biomedicine 19: 169-171, 1973
  22. Mimnaugh EG, et al Biochemical Pharmacology 35: 4327-4335, 1986
  23. Benjamin RS, et al Cancer Research 37: 1416-1420, 1977
  24. Legha SS, Hortobagyi GN, benjamin RS. Anthracyclines. In Lokich JJ (Ed) Cancer chemotherapy by infusion, pp. 100-113, Precept Press, Chicago, 1987
  25. Rudolph R, Journal of Clinical Oncology 5: 1116-1126, 1987
  26. Maral RJ, et al Cancer Treatment Reports 65 (Suppl. 4): 9-18, 1981

Chemical Properties

Adriamycin is an orange to red cake-like or needle-like crystalline solid.

Chemical Properties

Orange-Red Crystalline Solid

Uses

Used as an antineoplastic

Uses

Strong fluorescent dye intercalating into DNA. Antitumour antibiotic. Effect of adriamycin on heart mitochondrial DNA. Inhibitor of reverse transcriptase and RNA polymerase; immunosuppressive agent.

Uses

Antibacterial;DNA intercalant

Uses

Doxorubicin hydrochloride (adriamycin hydrochloride) is an antitumour agent that has been formulated as a salt to achieve higher water solubility. While the salt shares the same pharmacological properties as doxorubicin free base, its greater water solubility may offer advantages in some in vitro applications. Physicochemical properties and chromatographic behaviour will depend on whether the pH is buffered. In non-pH controlled systems the free base and salt may behave differently.

Uses

Doxorubicin is an anthracycline antitumor antibiotic that inhibits DNA topoisomerase II by inducing double-stranded DNA breaks. By intercalating within DNA, doxorubicin inhibits nucleic acid synthesis and induces apoptosis by inducing the accumulation of the p53 tumor suppressor protein.[Cayman Chemical]

brand name

Adriamycin (Pharmacia & Upjohn); Doxil (ALZA); Rubex (Bristol-Myers Squibb).

General Description

Orange-red thin needles. Aqueous solutions yellow-orange at acid pHs, orange-red at neutral pHs, and violet blue over pH 9.

General Description

Doxorubicin is available as both the conventional dosageform and a liposomal preparation, both of which are administeredby infusion. Doxorubicin HCl powder is available in10-, 20-, 50-, and 150-mg vials and is widely used in treatingvarious cancers, including leukemias, soft and bone tissuesarcomas, Wilms tumor, neuroblastoma, small cell lungcancer, and ovarian and testicular cancer.

Air & Water Reactions

Water soluble.

Reactivity Profile

Amines, like Doxorubicin hydrochloride, are weak chemical bases. They neutralize acids to form salts plus water. These acid-base reactions are exothermic. Amines may be incompatible with isocyanates, halogenated organics, peroxides, phenols (acidic), epoxides, anhydrides, and acid halides. Flammable gaseous hydrogen is generated by amines in combination with strong reducing agents, such as hydrides.

Fire Hazard

Doxorubicin hydrochloride is probably combustible.

Biological Activity

Antitumor antibiotic agent that inhibits DNA topoisomerase II. DNA intercalator that inhibits nucleic acid synthesis and induces apoptosis.

Potential Exposure

An antibiotic product from streptomyces, used as anticancer drug

Veterinary Drugs and Treatments

Doxorubicin is perhaps the most widely used antineoplastic agent at present in small animal medicine. It may be useful in the treatment of a variety of lymphomas, carcinomas, leukemias, and sarcomas in both the dog and cat, either alone or in combination protocols. Refer to the Dosage references or the Protocols found in the appendix for more information.

Shipping

UN2811 Toxic solids, organic, n.o.s., Hazard Class: 6.1; Labels: 6.1-Poisonous materials, Technical Name Required.

Incompatibilities

Incompatible with oxidizers (chlorates, nitrates, peroxides, permanganates, perchlorates, chlorine, bromine, fluorine, etc.); contact may cause fires or explosions. Keep away from alkaline materials, strong bases, strong acids, oxoacids, epoxides

Waste Disposal

It is inappropriate and possibly dangerous to the environment to dispose of expired or waste pharmaceuticals by flushing them down the toilet or discarding them to the trash. Household quantities of expired or waste pharmaceuticals may be mixed with wet cat litter or coffee grounds, double-bagged in plastic, discard in trash. Larger quantities shall carefully take into consideration applicable DEA, EPA, and FDA regulations. If possible return the pharmaceutical to the manufacturer for proper disposal being careful to properly label and securely package the material. Alternatively, the waste pharmaceutical shall be labeled, securely packaged and transported by a state licensed medical waste contractor to dispose by burial in a licensed hazardous or toxic waste landfill or incinerator.

Doxorubicin hydrochloride Preparation Products And Raw materials

Raw materials

Preparation Products

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Doxorubicin hydrochloride Suppliers

Dalian Meilun Biotech Co., Ltd.
Tel
0411-66771943;0411-66771942
Fax
0411-66771945
Email
sales@meilune.com
Country
China
ProdList
4046
Advantage
58
Shanghai Hao Yun Chemical Science Co.,Ltd.
Tel
021-68367562;021-68369562;15002147577
Fax
021-68369562
Email
sales@haoyunchem.com
Country
China
ProdList
455
Advantage
55
Beijing Zhongshuo Pharmaceutical Technology Development Co., Ltd
Tel
010-64430626/13801208576
Fax
010-64215766
Email
maggie@chinazhongshuo.com
Country
China
ProdList
210
Advantage
65
MedChemexpress LLC
Tel
609-228-6898
Fax
609-228-5909
Email
sales@medchemexpress.com
Country
United States
ProdList
4609
Advantage
58
Lancrix Chemicals
Tel
86-21-50817262
Fax
86-21-57712035
Email
sales@lancrix.com
Country
China
ProdList
1504
Advantage
55
Nanjing Sunlida Biological Technology Co., Ltd.
Tel
025-58378339;025-57798810
Fax
025-57019371
Email
sales@sunlidabio.com
Country
China
ProdList
3818
Advantage
55
Shanghai Hanjing Chemicals Co., Ltd.
Tel
+86 (21) 5428 5032
Fax
+86 (21) 5443 7651
Email
gerry.shu@hanjingchemicals.com
Country
China
ProdList
82
Advantage
55
Chemleader Biomedical Co., Limited.
Tel
400-968-3299 021-58180488
Fax
021-58180499-803
Email
sales@Medchemleader.com ; sales@Biochemleader.com
Country
China
ProdList
857
Advantage
58
BOC Sciences
Email
info@bocsci.com
Country
United States
ProdList
10507
Advantage
65
Shanghai TaoSu Biochemical Technology Co., Ltd.
Tel
021-33632979
Fax
021-33632979
Email
zijuecai@targetmol.com
Country
China
ProdList
2994
Advantage
58
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View Lastest Price from Doxorubicin hydrochloride manufacturers

Hebei Guanlang Biotechnology Co., Ltd.
Product
Doxorubicin hydrochloride 25316-40-9
Price
US $10.00/KG
Min. Order
1KG
Purity
99%
Supply Ability
10 mt
Release date
2019-07-02
NanJing Spring & Autumn Biological Engineering CO., LTD.
Product
Doxorubicin hydrochloride 25316-40-9 25316-40-9
Price
US $24.00/mg
Min. Order
20mg
Purity
≥98%
Supply Ability
1000.00 kgs
Release date
2019-07-16
career henan chemical co
Product
Doxorubicin hydrochloride 25316-40-9
Price
US $1.00/KG
Min. Order
1G
Purity
98%
Supply Ability
100KG
Release date
2018-08-20

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