ChemicalBook > Product Catalog >API >Mertansine

Mertansine

Mertansine Structure
CAS No.
139504-50-0
Chemical Name:
Mertansine
Synonyms
Maytansinoid dM 1;Mertansine (Maytansinoid DM 1);MERTANSINE; DM 1; MAYTANSINOID DM 1; 139504-50-0; UNII-DDZ29HGH0E; DM1 COMPOUND;;Mertansine;DM1 Compound;Maytansine DM1;DM1 Mertansine;Mertansine DMI;UNII-DDZ29HGH0E;The element DM1
CBNumber:
CB72684641
Molecular Formula:
C35H48ClN3O10S
Molecular Weight:
738.29
MOL File:
139504-50-0.mol
Modify Date:
2024/7/2 8:55:16

Mertansine Properties

Melting point 190-192℃ (decomposition)
Boiling point 937.1±65.0 °C(Predicted)
Density 1.33±0.1 g/cm3(Predicted)
storage temp. 2-8°C
solubility DMSO:60.0(Max Conc. mg/mL);81.26(Max Conc. mM)
form A crystalline solid
pka 9.82±0.70(Predicted)
color White to light yellow

Mertansine Chemical Properties,Uses,Production

Description

Maytansine, a natural alkaloid, was first isolated from Maydens ovale in 1972 and exists in the genus Maydens of the family Weedaceae and its relatives. The mechanism of action of maytansine, acting on microtubules and tubulin, blocks the formation of spindles in the process of cell mitosis by inhibiting the depolymerization of cell microtubules, and has a strong ability to inhibit tumor cell proliferation.

Chemical Properties

Mertansine is a white powder. It is soluble in organic solvents such as ethanol, DMSO, and dimethyl formamide (DMF), which should be purged with an inert gas. The solubility of mertansine in these solvents is approximately 0.25, 20, and 33 mg/ml, respectively.

Uses

Mertansine (DM1) is a microtubulin inhibitor which binds at the tips of microtubules and suppresses the dynamicity of microtubules.. Mertansine is an antibody-conjugatable maytansinoid that was developed to overcome systemic toxicity associated with maytansine and to enhance tumor-specific delivery. It can be attached to a monoclonal antibody with a linker to create an antibody-drug conjugate (ADC).

Definition

ChEBI: Mertansine is an organic heterotetracyclic compound and 19-membered macrocyclic lactam that is maytansine in which one of the hydrogens of the terminal N-acetyl group is replaced by a sulfanylmethyl group. It has a role as an antineoplastic agent and a tubulin modulator. It is an alpha-amino acid ester, a carbamate ester, an epoxide, an organic heterotetracyclic compound, an organochlorine compound, a thiol and a maytansinoid. It derives from a maytansine.

Biological Activity

Mertansine is a thiol-containing derivative of maytansine that is cytotoxic to human epidermoid carcinoma KB and human breast cancer SK-BR-3 cells (IC50 = 1.10 nM for both). Formulations containing mertansine have been studied for the treatment of multiple myeloma and squamous cell carcinoma.

Side effects

Dose-limiting toxicity was observed at 2 mg/m2, and was manifested as profound weakness, diarrhea, nausea, and vomiting.

Synthesis

Mertansine synthesis steps: A solution of N 2'-deacetyl-N 2'- (3-methyldithio-1-oxopropyl)- maytansine (2b) (1.95 g, 2.5 mmol) in a mixture of ethyl acetate (140 mL) and methanol (210 mL) was stirred at room temperature under an argon atmosphere and treated with a solution of dithiothreitol (0.95 g, 6.2 mmol) in 0.05 M potassium phosphate buffer (140 mL) at pH 7.5 containing 2 mM ethylenediaminetetraacetic acid (EDTA). The progress of the reaction was monitored by HPLC and was complete in three hours. The reaction mixture was treated with a solution of 0.2 M potassium phosphate buffer (250 mL) at pH 6.0 containing 2 mM EDTA and then extracted with ethyl acetate (3 x 600 mL). The organic layers were combined, washed with brine (100 mL), and then dried over sodium sulfate. Evaporation of the solvent gave a residue of crude thiol-containing maytansinoid 25a. The crude residue was purified by HPLC using a preparative Diazem cyano HPLC column (250 mm x 50 mm, 10 micron particle size) that was equilibrated in a mixture of hexanes/2-propanol/ethyl acetate (78.0:5.5:16.5, v/v/v) and run at a flow rate of 150 mL/min. The desired product 25a eluted as a peak centered at 16 min. The fractions containing the product were evaporated to give mertansine as a white solid (76% yield).
synthesis of Mertansine
Fig The synthetic method 1 of Mertansine.

Solubility in organics

Mertansine is soluble in organic solvents such as ethanol, DMSO, and dimethyl formamide (DMF). The solubility of mertansine in these solvents is approximately 0.25, 20, and 33 mg/ml, respectively. Mertansine is sparingly soluble in aqueous buffers. For maximum solubility in aqueous buffers, Mertansine should first be dissolved in DMF and then diluted with the aqueous buffer of choice. Mertansine has a solubility of approximately 0.03 mg/ml in a 1:30 solution of DMF: PBS(pH 7.2)using this method.

Mode of action

Mertansine is a 19-member ansa macrolide structure attached to a chlorinated benzene ring. It was originally isolated from the shrub Maytenus ovatus. The antimitotic effect of maytansine has been attributed to its ability to inhibit microtubule assembly by binding to tubulin with a KD of ~1 μmol/L, at or near the vinblastine-binding site. Mertansine is effective in vivo against Lewis lung carcinoma and B16 murine melanocarcinoma solid tumors and has antileukemic activity against P388 murine lymphocytic leukemia.

Mertansine Preparation Products And Raw materials

Global( 227)Suppliers
Supplier Tel Country ProdList Advantage Inquiry
CLEARSYNTH LABS LTD. +91-22-45045900 Hyderabad, India 6351 58 Inquiry
Pharmaffiliates Analytics and Synthetics P. Ltd +91-172-5066494 Haryana, India 6773 58 Inquiry
SynZeal Research Pvt Ltd +1 226-802-2078 Gujarat, India 6522 58 Inquiry
Pharma Affiliates 172-5066494 Haryana, India 6761 58 Inquiry
ATK CHEMICAL COMPANY LIMITED +undefined-21-51877795 China 32836 60 Inquiry
Fuxin Pharmaceutical +86-021-021-50872116 +8613122107989 China 10297 58 Inquiry
Xilinglab Co., Ltd. +8618381337976 China 86 58 Inquiry
Shanghai Daken Advanced Materials Co.,Ltd +86-371-66670886 China 18646 58 Inquiry
Henan Tianfu Chemical Co.,Ltd. +86-0371-55170693 +86-19937530512 China 21667 55 Inquiry
Hangzhou FandaChem Co.,Ltd. 008657128800458; +8615858145714 China 9337 55 Inquiry

Related articles

N2'-deacetyl-N2'-(3-Mercapto-1-oxopropyl)-Maytansine DM1 Mertansine Maytansine DM1 Maytansine, N2'-deacetyl-N2'-(3-mercapto-1-oxopropyl)- DM1 Compound UNII-DDZ29HGH0E (1S,2R,3S,5S,6S,16E,18E,20R,21S)-11-chloro-21-hydroxy-12,20-dimethoxy-2,5,9,16-tetramethyl-8,23-dioxo-4,24-dioxa-9,22-diazatetracyclo[19.3.1.110,14.03,5]hexacosa-10,12,14(26),16,18-pentaen-6-yl] (2S)-2-[methyl(3-sulfanylpropanoyl)amino]propanoate DM1 top3 N2'-deacetyl-N2'-(3-Mercapto-1-oxopropyl)-Maytansine USP/EP/BP MTBMertansine (DM1) Maytansinoid dM 1 MERTANSINE; DM 1; MAYTANSINOID DM 1; 139504-50-0; UNII-DDZ29HGH0E; DM1 COMPOUND; Mertansine (Maytansinoid DM 1) The element DM1 Propanedioicacid,2-(2-propyn-3-yl)-,diethylester Mertansine (14S,16S,32S,33S,2R,4S,10E,12E,14R)-86-Chloro-14-hydroxy-85,14-dimethoxy-33,2,7,10-tetramethyl-12,6-dioxo-7-aza-1(6,4)-oxazinana-3(2,3)-oxirana-8(1,3)-benzenacyclotetradecaphane-10,12-dien-4-yl N-(3-mercaptopropanoyl)-N-methyl-L-alaninate 13C,2H3]-Mertansine Maytansinoid DM-1,Maytansinoid DM 1,melanoma,Mertansine,Inhibitor,B16F10,ADC Payload,DM-1,ADC Cytotoxin,DM 1,tubulin,Microtubule/Tubulin,antiproliferative,inhibit,mitosis,antitumor,ADC Maytansinoid DM 1/ Mertansine Mertansine (DM1 Compound) Mertansine DMI N2'-deacetyl-N2'-(3-Mercapto-1-oxopropyl)-Maytansine 139504-50-0 C35H48ClN3O10S Antibody Drug Conjugates Inhibitors