MethylCBI-azaindole-benzamide-MOM-Boc-ethylenediamine-D - CAS 2222445-87-4

MethylCBI-azaindole-benzamide-MOM-Boc-ethylenediamine-D - CAS 2222445-87-4 Catalog number: BADC-01660

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MethylCBI-azaindole-benzamide-MOM-Boc-ethylenediamine-D is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs).

Category
ADCs Linker
Product Name
MethylCBI-azaindole-benzamide-MOM-Boc-ethylenediamine-D
CAS
2222445-87-4
Catalog Number
BADC-01660
Molecular Formula
C44H51ClN6O10
Molecular Weight
859.36

Ordering Information

Catalog Number Size Price Quantity
BADC-01660 -- $-- Inquiry
Description
MethylCBI-azaindole-benzamide-MOM-Boc-ethylenediamine-D is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs).
IUPAC Name
tert-butyl N-[2-[[(1S)-1-(chloromethyl)-3-[6-[[4-(methoxymethoxy)benzoyl]amino]imidazo[1,2-a]pyridine-2-carbonyl]-9-methyl-1,2-dihydrobenzo[e]indol-5-yl]oxycarbonyl-[2-(2-hydroxyethoxy)ethyl]amino]ethyl]-N-methylcarbamate
Canonical SMILES
CC1=C2C(=CC=C1)C(=CC3=C2C(CN3C(=O)C4=CN5C=C(C=CC5=N4)NC(=O)C6=CC=C(C=C6)OCOC)CCl)OC(=O)N(CCN(C)C(=O)OC(C)(C)C)CCOCCO
InChI
InChI=1S/C44H51ClN6O10/c1-28-8-7-9-33-36(60-43(56)49(18-20-58-21-19-52)17-16-48(5)42(55)61-44(2,3)4)22-35-39(38(28)33)30(23-45)24-51(35)41(54)34-26-50-25-31(12-15-37(50)47-34)46-40(53)29-10-13-32(14-11-29)59-27-57-6/h7-15,22,25-26,30,52H,16-21,23-24,27H2,1-6H3,(H,46,53)/t30-/m1/s1
InChIKey
VQQZUHVNVDPTLO-SSEXGKCCSA-N
Appearance
White to light yellow Solid

MethylCBI-azaindole-benzamide-MOM-Boc-ethylenediamine-D, a complex organic compound with promising applications in medicinal chemistry and drug discovery, holds great potential.

Drug Development: Serving as a foundational component in the synthesis of novel pharmaceuticals, MethylCBI-azaindole-benzamide-MOM-Boc-ethylenediamine-D offers a platform for creating derivatives with potentially heightened pharmacological properties. Researchers can manipulate its intricate molecular structure to explore diverse therapeutic avenues, aiming to enhance efficacy while mitigating adverse effects.

Cancer Research: Positioned at the forefront of cancer investigations, this compound is harnessed for its likely interactions with specific biological pathways crucial for tumor progression and proliferation. By scrutinizing its impacts on malignant cells, scientists can unveil underlying mechanisms and formulate targeted therapies.

Molecular Biology: Embraced in the realm of molecular biology, MethylCBI-azaindole-benzamide-MOM-Boc-ethylenediamine-D emerges as a valuable tool for delving into protein interactions and cellular processes. Its chemical attributes render it apt for assays exploring intra-cellular protein dynamics, unraveling essential insights into cellular functions and disease pathways essential for advancing our understanding of biological systems.

Synthetic Chemistry: As a versatile intermediary entity, this compound assumes a pivotal role in synthetic chemistry applications. It serves as a catalyst for exploring novel organic reactions and pathways, fostering the evolution of innovative synthesis methodologies. Chemists can harness its reactive nature to generate a diverse spectrum of chemical derivatives, expanding the repertoire of tools available for chemical synthesis and industrial applications.

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

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