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Doxorubicin

CAS No.
23214-92-8
Chemical Name:
Doxorubicin
Synonyms
DOXORUBICIN;Doxil;Rubex;Adriamycin PFS;HydroxydaunoMycin;Doxorubicin hydrohloride;10-((3-amino-2,3,6-trideoxy-alpha-l-lyso-hexopyranosyl)oxy)-7,8,9,10-tetrahydro-6,8,11-trihydroxy-8-(hydroxyacetyl)-1-methoxy-5,12-naphthacenedione;(1s,3s)-3,5,12-trihydroxy-3-(hydroxyacetyl)-10-methoxy-6,11-dioxo-1,2,3,4,6,11-hexahydrotetracen-1-yl 3-amino-2,3,6-trideoxy-alpha-l-lyxo-hexopyranoside;(8S-cis)-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-5,12-Naphthacenedione;(8S)-10-((4S,5S,6S)-4-amino-5-hydroxy-6-methyltetrahydro-2H-pyran-2-yloxy)-6,8,11-trihydroxy-8-(2-hydroxyacetyl)-1-methoxy-7,8,9,10-tetrahydrotetracene-5,12-dione
CBNumber:
CB00126300
Molecular Formula:
C27H29NO11
Molecular Weight:
543.53
MDL Number:
MFCD00869292
MOL File:
23214-92-8.mol
Last updated:2024-08-21 22:41:43

Doxorubicin Properties

Melting point 205°C
Boiling point 617.77°C (rough estimate)
Density 1.3783 (rough estimate)
refractive index 1.6400 (estimate)
storage temp. Keep in dark place,Sealed in dry,2-8°C
solubility ≥27.2 mg/mL in DMSO; insoluble in EtOH; ≥24.8 mg/mL in H2O with ultrasonic
form solid
pka pKa 8.2 (Uncertain)
Water Solubility Soluble
CAS DataBase Reference 23214-92-8
EWG's Food Scores 5
NCI Dictionary of Cancer Terms Adriamycin PFS; Adriamycin RDF; Doxil
FDA UNII 80168379AG
NCI Drug Dictionary Doxil
ATC code L01DB01
IARC 2A (Vol. 10, Sup 7) 1987
EPA Substance Registry System Doxorubicin (23214-92-8)

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictogramsGHS hazard pictograms
GHS07,GHS08
Signal word  Danger
Hazard statements  H302-H315-H319-H335-H350-H362
Precautionary statements  P260-P263-P280
HS Code  2941900000
Toxicity An anthracycline cytotoxic antineoplastic that is produced by Streptomyces peucetius. The LD50 in mice is 9.4 mg/kg, i.v. It is a carcinogen that inhibits DNA and RNA synthesis by intercalating in double-stranded DNA with the amino sugar in the minor groove and the 90-OH group of the anthracycline ring hydrogen-bonded to the adjacent guanine. It also alters membrane fluidity and ion transport, and generates free radicals through a cytochrome P450-mediated reductive process. In humans, it causes alopecia, stomatitis, nausea, vomiting, diarrhea, cardiotoxicity (manifested by tachycardia), and potentially fatal congestive heart failure.

Doxorubicin price

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Usbiological 489423 PROK2 23214-92-8 100ul $499 2021-12-16 Buy
Usbiological D9099-43 Doxorubicin 23214-92-8 25mg $515 2021-12-16 Buy
Usbiological 358143 PK2 23214-92-8 48Tests $588 2021-12-16 Buy
Usbiological 358144 PK2 23214-92-8 48Tests $588 2021-12-16 Buy
Usbiological 384073 PK2 23214-92-8 96Tests $729 2021-12-16 Buy
Product number Packaging Price Buy
489423 100ul $499 Buy
D9099-43 25mg $515 Buy
358143 48Tests $588 Buy
358144 48Tests $588 Buy
384073 96Tests $729 Buy

Doxorubicin Chemical Properties,Uses,Production

Uses

Doxorubicin is in a class of medications called anthracyclines. It works by slowing or stopping the growth of cancer cells in your body. Doxorubicin is used in combination with other medications to treat certain types of the bladder, breast, lung, stomach, and ovarian cancer; Hodgkin's lymphoma (Hodgkin's disease) and non-Hodgkin's lymphoma (cancer that begins in the cells of the immune system); and certain types of leukemia (cancer of the white blood cells), including acute lymphoblastic leukemia (ALL) and acute myeloid leukemia (AML, ANLL).
Doxorubicin is also used alone and in combination with other medications to treat certain types of thyroid cancer and certain types of soft tissue or bone sarcomas (cancer that forms in muscles and bones). It is also used to treat neuroblastoma (a cancer that begins in nerve cells and occurs mainly in children) and Wilms' tumor (a type of kidney cancer that occurs in children).

Mechanism of action

There are two proposed mechanisms by which doxorubicin acts in the cancer cell: (i) intercalation into DNA and disruption of topoisomerase-II-mediated DNA repair and (ii) generation of free radicals and damage to cellular membranes, DNA, and proteins. In brief, doxorubicin is oxidized to semiquinone, an unstable metabolite, which is converted back to doxorubicin in a process that releases reactive oxygen species. Reactive oxygen species can lead to lipid peroxidation and membrane damage, DNA damage, oxidative stress, and trigger apoptotic pathways of cell death. Candidate genes that may modulate this pathway involve those capable of the oxidation reaction (NADH dehydrogenases, nitric oxide synthases, xanthine oxidase) and those capable of deactivating the free radicals such as glutathione peroxidase, catalase, and superoxide dismutase. Alternatively, doxorubicin can enter the nucleus and poison topoisomerase-II, resulting in DNA damage and cell death.
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Side effects

Adverse reactions are common after doxorubicin administration, including fatigue, alopecia, nausea and vomiting, and oral sores. Bone marrow suppression and an increased risk of secondary malignancy diagnoses may occur.

antibiotic

Doxorubicin is an antibiotic derived from the Streptomyces peucetius bacterium. It has been widely used as a chemotherapeutic agent since the 1960s. Doxorubicin is part of the anthracycline group of chemotherapeutic agents. Doxorubicin may be used to treat soft tissue and bone sarcomas and cancers of the breast, ovary, bladder, and thyroid. It also treats acute lymphoblastic leukemia, acute myeloblastic leukemia, Hodgkin lymphoma, and small-cell lung cancer.

25316-40-9
23214-92-8
Synthesis of Doxorubicin from Doxorubicin hydrochloride

Doxorubicin Preparation Products And Raw materials

Global( 258)Suppliers
Supplier Tel Email Country ProdList Advantage
Shaanxi Dideu Medichem Co. Ltd
+86-29-81148696 +86-15536356810 1022@dideu.com China 3878 58
Hebei Mojin Biotechnology Co., Ltd
+86 13288715578 +8613288715578 sales@hbmojin.com China 12495 58
Shaanxi TNJONE Pharmaceutical Co., Ltd
+8618092446649 sarah@tnjone.com China 1143 58
Henan Tianfu Chemical Co.,Ltd.
+86-0371-55170693 +86-19937530512 info@tianfuchem.com China 21663 55
career henan chemical co
+86-0371-86658258 +8613203830695 sales@coreychem.com China 29888 58
Shenzhen Nexconn Pharmatechs Ltd
+86-755-89396905 +86-15013857715 admin@nexconn.com China 10311 58
Accela ChemBio Inc.
+1-858-6993322 info@accelachem.com United States 19563 58
Hebei Guanlang Biotechnology Co., Ltd.
+86-19930503282 alice@crovellbio.com China 8820 58
Chongqing Chemdad Co., Ltd
+86-023-6139-8061 +86-86-13650506873 sales@chemdad.com China 39916 58
CONIER CHEM AND PHARMA LIMITED
+8618523575427 sales@conier.com China 49392 58

View Lastest Price from Doxorubicin manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Doxorubicin pictures 2024-04-15 Doxorubicin
23214-92-8
US $0.00 / kg 1kg 99% 20tons Shaanxi TNJONE Pharmaceutical Co., Ltd
Doxorubicin hydrochloride pictures 2021-11-02 Doxorubicin hydrochloride
25316-40-9
US $95.00 / g 1g 99% 100KG Baoji Guokang Healthchem co.,ltd
Doxorubicin hydrochloride / Doxorubicin hcl pictures 2021-05-14 Doxorubicin hydrochloride / Doxorubicin hcl
25316-40-9
US $1.00 / PCS 1KG 99% 10 mt Hebei Guanlang Biotechnology Co., Ltd.
  • Doxorubicin pictures
  • Doxorubicin
    23214-92-8
  • US $0.00 / kg
  • 99%
  • Shaanxi TNJONE Pharmaceutical Co., Ltd

Adriamycin Spectrum

5,12-Naphthacenedione, 10-[(3-amino-2,3,6-trideoxy-α-L-lyxo-hexopyranosyl)oxy]-7,8,9,10-tetrahydro-6,8,11-trihydroxy-8-(2-hydroxyacetyl)-1-methoxy-, (8S,10S)- ADRIAMYCIN 14-Hydroxydaunomycin adiblastine (hydrochloride salt) adriablastine (hydrochloride salt) adriablatina (hydrochloride salt) Adriacin (hydrochloride salt) Adriamycin PFS (hydrochloride salt) Adriamycin RDF Adriamycin RDF (hydrochloride salt) Adriblastin Adriblastina (hydrochloride salt) adriblatina (hydrochloride salt) Doxorubicin hydrochloride (hydrochloride salt) Farmablastina (hydrochloride salt) Hydroxydaunomycin hydrochloride (hydrochloride salt) Hydroxydaunorubicin hydrochloride (hydrochloride salt) Rubex (hydrochloride salt) 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-, (8S,10S)- 5,12-Naphthacenedione, 10-[(3-amino-2,3,6-trideoxy-a-L-lyxo-hexopyranosyl)oxy]-7,8,9,10-tetrahydro-6,8,11-trihydroxy-8-(2-hydroxyacetyl)-1-methoxy-, (8S,10S)- 5,12-Naphthacenedione, 10-[(3-amino-2,3,6-trideoxy-α-L-lyxo-hexopyranosyl)oxy]-7,8,9,10-tetrahydro-6,8,11-trihydroxy-8-(hydroxyacetyl)-1-methoxy-, (8S,10S)- 5,12-Naphthacenedione, 10-[(3-amino-2,3,6-trideoxy-α-L-lyxo-hexopyranosyl)oxy]-7,8,9,10-tetrahydro-6,8,11-trihydroxy-8-(hydroxyacetyl)-1-methoxy-, (8S-cis)- NSC 123127 ADRIAMYCINSEMIQUINONE (85-cis)-10-[(3-amino-2,3,6-trideoxy-alpha-l-lyxohexapyranosyl)oxy]-7,8,9,10- t adriamycine etrahydro-6,8,11-trihydroxy-8-(hydroxyacetyl)-1-methoxy-5,12-naphthacenedione DOXOPINHYDROCHLORIDE (85-Cis)-10-Tetrahydro-6,8,11-Trihydroxy-8-(Hydroxyacetyl)-1-methoxy-5,12-Naphthacenedione (8S,10S)-10-[(3-Amino-2,3,6-trideoxy-α-L-lyxo-hexopyranosyl)oxy]-8-glycoloyl-7,8,9,10-tetrahydro-6,8,11-trihydroxy-1-methoxy-5,12-naphthacenedione NCI-C-01514 10-((3-AMino-2,3,6-trideoxy-α-L-lyso-hexopyranosyl)oxy)-7,8,9,10-tetrahydro-6,8,11-trihydroxy-8-(hydroxyacetyl)-1-Methoxy-5,12-naphthacenedione Doxorubicin base (8S,10S)-10-{[(2R,4S,5S,6S)-4-aMino-5-hydroxy-6-Methyloxan-2-yl]oxy}-6,8,11-trihydroxy-8-(2-hydroxyacetyl)-1-Methoxy-5,7,8,9,10,12-hexahydrotetracene-5,12-dione Biotransdox Evacet PK 2 Rubidox Doxorubicin Free Base Doxorubincine AdriaMycin, 14-HydroxydaunoMycin, FI 106, K 1039, KW 125, NSC 123127 PROK2 Prokineticin-2 human Protein Bv8 homolog ADRIAMYCIN, PHARMA Adriamycin Adriamycin Adriamycin,98% Doxolem oxorubicin Adriamycin USP/EP/BP Hydroxydaunorubicin Doxorubicin trifluoroacetate salt Epirubicin hydrochloride EP Impurity C Doxorubicin 13CD3Q: What is Doxorubicin 13CD3 Q: What is the CAS Number of Doxorubicin 13CD3 Q: What is the storage condition of Doxorubicin 13CD3 Q: What are the applications of Doxorubicin 13CD3 DoxorubicinQ: What is Doxorubicin Q: What is the CAS Number of Doxorubicin Q: What is the storage condition of Doxorubicin Adriamycin 23214-92-8 5,12-Naphthacenedione, 10-[(3-amino-2,3,6-trideoxy-α-L-lyxo-hexopyranosyl)oxy]-7,8,9,10-tetrahydro-6,8,11-trihydroxy-8-(2-hydroxyacetyl)-1-methoxy-, (8S,10S)- Doxorubicin hydrohloride