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DM1 (Mertansine) Microtubule Associated inhibitor

Cat.No.S6773

DM1 (Mertansine), an antibody-conjugatable maytansinoid, is a selective microtubule inhibitor developed to overcome systemic toxicity associated with maytansine and to enhance tumour-specific delivery. It can be attached to a monoclonal antibody with a linker to create an antibody-drug conjugate (ADC).Solutions are unstable and should be fresh-prepared.
DM1 (Mertansine) Microtubule Associated inhibitor Chemical Structure

Chemical Structure

Molecular Weight: 738.29

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Quality Control

Batch: S677301 DMSO]50 mg/mL]false]Ethanol]2 mg/mL]false]Water]Insoluble]false Purity: 99.84%
99.84

Chemical Information, Storage & Stability

Molecular Weight 738.29 Formula

C35H48ClN3O10S

Storage (From the date of receipt) 3 years-20°C powder
CAS No. 139504-50-0 -- Storage of Stock Solutions Solutions are unstable. Prepare fresh or purchase small, pre-packaged sizes. Repackage upon receipt.
Synonyms Maytansinoid DM1 Smiles COC1\C=C\C=C(C)\CC2=CC(=C(Cl)C(=C2)OC)N(C)C(=O)CC(OC(=O)C(C)N(C)C(=O)CCS)C3(C)OC3C(C)C4CC1(O)NC(=O)O4

Solubility

In vitro
Batch:

DMSO : 50 mg/mL (67.72 mM)
(Moisture-contaminated DMSO may reduce solubility. Use fresh, anhydrous DMSO.)

Ethanol : 2 mg/mL

Water : Insoluble

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Mass Concentration Volume Molecular Weight
Dilution Calculator Molecular Weight Calculator

In vivo
Batch:

In vivo Formulation Calculator (Clear solution)

Step 1: Enter information below (Recommended: An additional animal making an allowance for loss during the experiment)

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Step 2: Enter the in vivo formulation (This is only the calculator, not formulation. Please contact us first if there is no in vivo formulation at the solubility Section.)

% DMSO % % Tween 80 % ddH2O
%DMSO %

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Working concentration: mg/ml;

Method for preparing DMSO master liquid: mg drug pre-dissolved in μL DMSO ( Master liquid concentration mg/mL, Please contact us first if the concentration exceeds the DMSO solubility of the batch of drug. )

Method for preparing in vivo formulation: Take μL DMSO master liquid, next addμL PEG300, mix and clarify, next addμL Tween 80, mix and clarify, next add μL ddH2O, mix and clarify.

Method for preparing in vivo formulation: Take μL DMSO master liquid, next add μL Corn oil, mix and clarify.

Note: 1. Please make sure the liquid is clear before adding the next solvent.
2. Be sure to add the solvent(s) in order. You must ensure that the solution obtained, in the previous addition, is a clear solution before proceeding to add the next solvent. Physical methods such as vortex, ultrasound or hot water bath can be used to aid dissolving.

Mechanism of Action

Targets/IC50/Ki
Microtubule
References

Clinical Trial Information

(data from https://clinicaltrials.gov, updated on 2024-05-22)

NCT Number Recruitment Conditions Sponsor/Collaborators Start Date Phases
NCT06138743 Recruiting
Myotonic Dystrophy 1
Arrowhead Pharmaceuticals
March 4 2024 Phase 1
NCT05532813 Not yet recruiting
Steinert''s Disease|Myotonic Dystrophy 1|Metformin
Assistance Publique - Hôpitaux de Paris
March 2024 Phase 3
NCT06204809 Recruiting
Myotonic Dystrophy 1
PepGen Inc
December 12 2023 Phase 1
NCT06270186 Withdrawn
Myotonic Dystrophy 1
Centre Hospitalier Universitaire de Nice
November 2023 Not Applicable
NCT05945927 Recruiting
Breast Cancer
Hoffmann-La Roche
September 13 2023 --

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