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MITHRAMYCIN A

MITHRAMYCIN A Structure
CAS No.
18378-89-7
Chemical Name:
MITHRAMYCIN A
Synonyms
MITHRAMYCIN;PLICAMYCIN;2371;pa144;mitramycin;a-2371;nsc24559;MITHRACIN;luteomycin;aurelicacid
CBNumber:
CB9127380
Molecular Formula:
C52H76O24
Molecular Weight:
1085.15
MOL File:
18378-89-7.mol
MSDS File:
SDS
Modify Date:
2024/3/16 17:05:46

MITHRAMYCIN A Properties

Melting point 180-183 °C
alpha D20 -51° (c = 0.4 in ethanol)
Boiling point 761.72°C (rough estimate)
Density 1.1576 (rough estimate)
refractive index 1.6500 (estimate)
storage temp. 2-8°C
solubility Soluble in DMSO (up to 20 mg/ml) or in Ethanol (up to 10 mg/ml)
form Powder
pka 4.54±0.60(Predicted)
color Red to brown
Merck 13,7619
BRN 5236667
Stability Stable for 1 year from date of purchase as supplied. Solutions in DMSO or ethanol may be stored at -20°C for up to 1 month.
EPA Substance Registry System Plicamycin (18378-89-7)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS07
Signal word  Warning
Hazard statements  H302
Precautionary statements  P301+P312+P330
Hazard Codes  Xn,T+
Risk Statements  22-26/27/28
Safety Statements  45-38-36/37/39-28A-22
RIDADR  3249
WGK Germany  3
RTECS  PZ2800000
10
HazardClass  6.1(b)
PackingGroup  III
HS Code  29419090
Toxicity LD50 in mice, rats (mg/kg): 2.14, 1.74 i.v. (Slavik, Carter)
NFPA 704
0
2 0

MITHRAMYCIN A price More Price(2)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich(India) M6891 Mithramycin A from Streptomyces plicatus ≥90% (HPLC) 18378-89-7 1MG ₹20578.33 2022-06-14 Buy
Sigma-Aldrich(India) M6891 Mithramycin A from Streptomyces plicatus ≥90% (HPLC) 18378-89-7 5MG ₹84738.1 2022-06-14 Buy
Product number Packaging Price Buy
M6891 1MG ₹20578.33 Buy
M6891 5MG ₹84738.1 Buy

MITHRAMYCIN A Chemical Properties,Uses,Production

Description

Mithramycin is an antineoplastic antibiotic produced by Streptomyces plicatus. It is well known as the aureolic acid antitumor antibiotic that inhibits both cancer growth and bone resorption by cross-linking GC-rich DNA, thus blocking binding of Sp-family transcription factors to gene regulatory elements. Transcription of c-Src, a gene implicated in many human cancers and required for osteoclast-dependent bone resorption, is regulated by the binding of Sp factors to specific elements in its promoter. Therefore, this gene represents an important anticancer target and a potential lead target through which mithramycin displays action against osteoclastic bone resorption via an unknown mechanism. Hazards of handling this drug by the health-care personnel arise from a combination of factors: (1) its inherent toxicity and (2) the extent to which workers are exposed to the drug in the course of carrying out their duties. This exposure may be through inadvertent ingestion of the drug on foodstuffs (e.g., workers’ lunches), inhalation of drug dusts or droplets, or direct skin contact. Mithramycin has been used to decrease bone resorption in patients with humoral hypercalcemia and Paget’s disease.

Chemical Properties

yellow powder

Uses

Mithramycin was the first of the aureolic acid class of antitumour antibiotics, isolated from Streptomyces. Mithramycin inhibits transcription and protein synthesis by non-covalent binding with G-C-rich duplex DNA in the presence of magnesium and zinc ions. Mithramycin also induces differentiation of leukemic cells accompanied by an early decrease in c-myc expression, and selectively inhibits collagen-1 gene expression in human fibroblasts.

Indications

Plicamycin (mithramycin, Mithracin) is one of the chromomycin group of antibiotics produced by Streptomyces tanashiensis. Plicamycin binds to DNA and inhibits transcription. It also inhibits resorption of bone by osteoblasts, thus lowering serum calcium levels.Very little is known about its distribution, metabolism, and excretion. Because of its severe toxicity, plicamycin has limited clinical utility.The major indication for plicamycin therapy is in the treatment of life-threatening hypercalcemia associated with malignancy. Plicamycin also can be used in the palliative therapy of metastatic testicular carcinoma when all other known active drugs have failed.

Application

Mithramycin, recently renamed plicamycin, was found in the culture broth of Streptomyces argillaceus and S. tanashiensis by Abbott Laboratories in 1952. It is structurally related to chromomycin A3. Mithramycin shows strong inhibitory activity against malignant cells of human origin. It acts by inhibition of the DNA-directed RNA synthesis through binding with DNA. Mithramycin is used intravenously to treat cancers of the embryonal cells, seminoma, choriocarcinoma, etc.

General Description

Chemical structure: aureolic acid

Biological Activity

Anticancer antibiotic that selectively binds to G-C-rich DNA in the presence of Mg 2+ or Zn 2+ , inhibiting RNA and DNA polymerase action. Inhibits c-myc expression and induces myeloid differentiation of HL-60 promyelocytic leukemia cells.

Purification Methods

Purify mithramycin A by crystallisation from CHCl3. It is soluble in MeOH, EtOH, Me2CO, EtOAc, Me2SO and H2O, and moderately soluble in CHCl3, but is slightly soluble in *C6H6 and Et2O. It is a fluorescent antitumour agent used in flow cytometry. [Thiem & Meyer Tetrahedron 37 551 1981, NMR: Yu et al. Nature 218 193 1968, Beilstein 17/1 V 672.]

MITHRAMYCIN A Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 175)Suppliers
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AFINE CHEMICALS LIMITED +86-0571-85134551 China 15395 58 Inquiry
AUREOLIC ACID METHRAMYCIN A MITHRAMYCIN A, FOR FLUORESCENCE MITHRAMYCIN A FROM STREPTOMYCES*PLICATUS APPROX. 96 MITHRAMYCIN COMPLEX FROM STREPTOMYCES*PL ICATUS MITHRAMYCIN FROM STREPTOMYCES PLICATUS MITHRACIN MITHRAMYCIN A MITHRAMYCIN A, STREPTOMYCES PLICATUS (2s-alpha,3beta(1r*,3r*4s*)))-droxy-7-methyl 1(2h)-anthracenone,6-((2,6-dideoxy-3-o-(2,6-dideoxy-beta-d-arabino-hexopyranos 6-dideoxy-alpha-d-lyxo-hexpyranosyl-(1-3)-2,6-dideoxy-beta-d-arabino-4)-o-2 a-2371 antibioticla7017 aurelicacid aurlelicacid hexpyranosyl)oxy)-3-(3,4-dihydroxy-1-methoxy-2-oxopentyl)-3,4-dihydro-8,9-dihy nsc24559 yl)-beta-d-arabino-h)-2-((o-2,6-dideoxy-3-c-methyl-beta-d-ribohexopyranosyl-( D-threo-2-Pentulose, 5-deoxy-1-C-(2S,3S)-7-2,6-dideoxy-3-O-(2,6-dideoxy-.beta.-D-arabino-hexopyranosyl)-.beta.-D-arabino-hexopyranosyloxy-3-(O-2,6-dideoxy-3-C-methyl-.beta.-D-ribo-hexopyranosyl-(1?3)-O-2,6-dideoxy-.beta.-D-lyxo-hexopyranosyl-(1?3)-2,6-did mithramycin a from streptomyces plicatus Mithramycin, Aureolic acid, Plicamycin Mithramycin A from Streptomyces argillaceus Aureolic acid, Plicamycin (2S-(2alpha,3beta(1R*,3R*,4S*)))-6-((2,6-Dideoxy-3-O-(2,6-dideoxy-beta-D-arabino-hexopyranosyl)-beta-D-arabino-hexopyranosyl)oxy)-2-((O-2,6-dideoxy-3-C-methyl-beta-D-ribo-hexopyranosyl-(1->4)-O-2,6-dideoxy-alpha-D-lyxo-hexopyranosyl-(1->3)-2,6-dideoxy-bet Mithramycin,90% Plicamycin(Mithramycin) (1S)-5-Deoxy-1-C-[(2S,3S)-7-[[2,6-dideoxy-3-O-(2,6-dideoxy-β-D-arabino-hexopyranosyl)-β-D-arabino-hexopyranosyl]oxy]-3-[(O-2,6-dideoxy-3-C-methyl-β-D-ribo-hexopyranosyl-(1.fwdarw.3)-O-2,6-dideoxy-β-D-lyxo-hexopyranosyl-(1.fwdarw.3)-2,6-dideoxy-β-D-arabino-hexopyranosyl)oxy]-1,2,3,4-tetrahydro-5,10-dihydroxy-6-methyl-4-oxo-2-anthracenyl]-1-O-methyl-D-threo-2-pentulose Plicamycin (50 mg) (1S)-5-Deoxy-1-C-[(2S,3S)-7-[[2,6-dideoxy-3-O-(2,6-dideoxy-β-D-arabino-hexopyranosyl)-β-D-arabino-hexopyranosyl]oxy]-3-[(O-2,6-dideoxy-3-C-Methyl-β-D-ribo-hexopyranosyl-(1.fwdarw.3)-O-2,6-dideoxy-β-D-lyxo-hexopyranosyl-(1.fwdarw.3)-2,6-dideo [1S(2S,3S)]-5-Deoxy-1-C-[7-[[2,6-dideoxy-3-O-(2,6-dideoxy-β-D-arabino-hexopyranosyl)-β-D-arabino-hexopyranosyl]oxy]-3-[(O-2,6-dideoxy-3-C-Methyl-β-D-ribo-hexopyranosyl-(1→3)-O-2,6-dideoxy-β-D-arabino-hexopyranosyl-(1→3)-2,6-dideoxy-β-D-lyxo-hexopyranosyl)oxy]-1,2,3,4-tetrahydro-5,10-dihydroxy-6-Methyl-4-oxo-2-anthracenyl]-1-O-Methyl-D-threo-2-pentulose PlicatoMycin Aureolic acid, Mithracin, PlicaMycin, MitraMycin, A 2371, LA 7017, NSC 23559, PA 144 MTM, Mithramycin A Plicamycin, BC D-threo-2-Pentulose, 5-deoxy-1-C-[(2S,3S)-7-[[2,6-dideoxy-3-O-(2,6-dideoxy-β-D-arabino-hexopyranosyl)-β-D-arabino-hexopyranosyl]oxy]-3-[(O-2,6-dideoxy-3-C-methyl-β-D-ribo-hexopyranosyl-(1→3)-O-2,6-dideoxy-β-D-lyxo-hexopyranosyl-(1→3)-2,6-dideoxy-β-D-arabino-hexopyranosyl)oxy]-1,2,3,4-tetrahydro-5,10... MITHRAMYCIN A USP/EP/BP MITHRAMYCIN PLICAMYCIN mitramycin pa144 2371 Mithramycin (Plicamycin) luteomycin 18378-89-7 C52H76O24 BioChemical Antibiotics Antibiotics G-M Antibiotics A to Z antibiotic Antibiotics Antitumour