webinar
Oct. 27-28, 2025, Boston, MA, USA - Booth 114.
Read More

DM4-SMCC

  CAS No.: 1228105-52-9   Cat No.: BADC-00017   Purity: ≥98% 4.5  

DM4 with a reactive linker SMCC, which can react with antibody to make antibody drug conjugate. DM4 can bind to tubulin at or near the vinblastine-binding site.

DM4-SMCC

Structure of 1228105-52-9

Quality
Assurance

Worldwide
Delivery

24/7 Customer
Support
Category
ADC Cytotoxin
Molecular Formula
C54H72ClN5O16S
Molecular Weight
1114.69
Shipping
Room temperature
Shipping
-18°C for long term storage, avoid light.

* For research and manufacturing use only. We do not sell to patients.

Size Price Stock Quantity
-- $-- In stock

Looking for different specifications? Click to request a custom quote!

Capabilities & Facilities

Popular Publications Citing BOC Sciences Products
Synonyms
Maytansinoid DM4- succinimidyl 4-(N-maleimidomethyl)cyclohexane-1-carboxylate
IUPAC Name
(2,5-dioxopyrrolidin-1-yl) 4-[[3-[5-[[(2S)-1-[[(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]oxy]-1-oxopropan-2-yl]-methylamino]-2-methyl-5-oxopentan-2-yl]sulfanyl-2,5-dioxopyrrolidin-1-yl]methyl]cyclohexane-1-carboxylate
Canonical SMILES
CC1C2CC(C(C=CC=C(CC3=CC(=C(C(=C3)OC)Cl)N(C(=O)CC(C4(C1O4)C)OC(=O)C(C)N(C)C(=O)CCC(C)(C)SC5CC(=O)N(C5=O)CC6CCC(CC6)C(=O)ON7C(=O)CCC7=O)C)C)OC)(NC(=O)O2)O
InChI
InChI=1S/C54H72ClN5O16S/c1-29-12-11-13-39(72-10)54(70)27-37(73-51(69)56-54)30(2)47-53(6,75-47)40(26-44(64)58(8)35-23-33(22-29)24-36(71-9)46(35)55)74-49(67)31(3)57(7)41(61)20-21-52(4,5)77-38-25-45(65)59(48(38)66)28-32-14-16-34(17-15-32)50(68)76-60-42(62)18-19-43(60)63/h11-13,23-24,30-32,34,37-40,47,70H,14-22,25-28H2,1-10H3,(H,56,69)/b13-11+,29-12+/t30-,31+,32?,34?,37+,38?,39-,40+,47+,53+,54+/m1/s1
Solubility
10 mm in DMSO
Appearance
Soild powder
Shelf Life
Powder: -20°C 3 years; In solvent: -80°C 6 months
Shipping
Room temperature
Storage
-18°C for long term storage, avoid light.

DM4-SMCC is a potent cytotoxic agent used in the development of antibody-drug conjugates (ADCs). Here are some key applications of DM4-SMCC:

Cancer Therapy: DM4-SMCC is utilized in the creation of ADCs that specifically target cancer cells, delivering the cytotoxic drug directly to the tumor site. By linking DM4-SMCC to monoclonal antibodies that recognize cancer-specific markers, targeted killing of cancer cells is achieved while sparing healthy cells, thus reducing side effects. This targeted approach increases the therapeutic index and efficacy of cancer treatments.

Target Validation: In preclinical studies, DM4-SMCC can be used to validate potential therapeutic targets. By conjugating DM4-SMCC to antibodies against new tumor markers, researchers can evaluate the effectiveness of targeting those markers in cell and animal models. This helps in identifying promising targets for the development of new cancer therapies.

Drug Resistance Research: DM4-SMCC is instrumental in studying mechanisms of drug resistance in cancer cells. By using ADCs containing DM4-SMCC, researchers can investigate how cancer cells develop resistance to targeted cytotoxic agents. This knowledge contributes to the design of next-generation ADCs with improved resistance profiles.

Pharmacokinetics and Toxicology Studies: DM4-SMCC is employed in pharmacokinetic and toxicology studies to assess the distribution, metabolism, and potential toxic effects of ADCs. By studying the behavior of DM4-SMCC conjugates in biological systems, researchers can optimize dosing regimens and enhance the safety profile of ADC-based therapies. This is essential for the successful translation of ADCs from bench to bedside.

The molarity calculator equation

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

The dilution calculator equation

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

Related Products

Contact our experts today for pricing and comprehensive details on our ADC offerings.

You May Also Be Interested In

From cytotoxin synthesis to linker design, discover our specialized services that complement your ADC projects.

ADC Payload Development Biological Payload Chemical Payload Protein Toxin Nanocarrier Microtubule Inhibitors DNA Damaging Agents RNA Polymerase Inhibitors Protein Degraders

Unlock Deeper ADC Insights

Learn more about payload design, linker strategies, and integrated CDMO support through our curated ADC content.

Maytansine and Its Analogues Cytotoxic Agents Used in Antibody–Drug Conjugates Exatecan Mesylate in ADCs: A New Topo I Inhibitor What is Calicheamicin? What is Monomethyl Auristatin E (MMAE)? What is Monomethyl Auristatin F (MMAF)? What is Pyrrolobenzodiazepine (PBD)? Antiviral Potential of Thapsigargin in COVID-19 Research ADC Payloads Explained: Current Types and Cutting-Edge Research Progress Tubulin Inhibitors - Highly Potential ADC Payloads

Explore More ADC Products

Find exactly what your project needs from our expanded range of ADCs, offering flexible options to fit your timelines and goals.

ADC Cytotoxin

Powerful Targeted Cancer Solutions

ADC  Cytotoxin with Linker

Enhanced Stability And Efficacy

ADC Linker

Precise Conjugation For Success

Antibody-Drug  Conjugates (ADCs)

Maximized Therapeutic Performance

Auristatins

Next-Level Tubulin Inhibition

Calicheamicins

High-Impact DNA Targeting

Camptothecins

Advanced Topoisomerase Inhibition

Daunorubicins / Doxorubicins

Trusted Anthracycline Payloads

Duocarmycins

Potent DNA Alkylation Agents

Maytansinoids

Superior Microtubule Disruption

Pyrrolobenzodiazepines

Ultra-Potent DNA Crosslinkers

Traditional Cytotoxic Agents

Proven Chemotherapy Solutions

Cleavable Linker

Precise Intracellular Drug Release

Non-Cleavable Linker

Exceptional Long-Term Stability

Historical Records: Imperatoxin-Inhibitor | AZ1508 | Me-triacetyl-β-D-glucopyranuronate-Ph-CH2OH-Fmoc | DM4-SMCC
Send Inquiry
Verification code
Inquiry Basket