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Boc-C2-Urea-bis(Boc)-C4-Urea-4-phenylacetic acid

  CAS No.: 1610413-97-2   Cat No.: BADC-01712 4.5  

Boc-C2-Urea-bis(Boc)-C4-Urea-4-phenylacetic acid is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs).

Boc-C2-Urea-bis(Boc)-C4-Urea-4-phenylacetic acid

Structure of 1610413-97-2

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ADC Linker
Molecular Formula
C34H54N4O10
Molecular Weight
678.81

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Synonyms
2-(4-((9S,13S)-9,13-Bis(tert-butoxycarbonyl)-18,18-dimethyl-3,11,16-trioxo-17-oxa-2,4,10,12-tetraazanonadecyl)phenyl)acetic acid; L-Glutamic acid, N-[[[(1S)-5-[[[[[4-(carboxymethyl)phenyl]methyl]amino]carbonyl]amino]-1-[(1,1-dimethylethoxy)carbonyl]pentyl]amino]carbonyl]-, 1,5-bis(1,1-dimethylethyl) ester; PSMA-ligand-1
IUPAC Name
2-[4-[[[(5S)-5-[[(2S)-1,5-bis[(2-methylpropan-2-yl)oxy]-1,5-dioxopentan-2-yl]carbamoylamino]-6-[(2-methylpropan-2-yl)oxy]-6-oxohexyl]carbamoylamino]methyl]phenyl]acetic acid
Canonical SMILES
CC(C)(C)OC(=O)CCC(C(=O)OC(C)(C)C)NC(=O)NC(CCCCNC(=O)NCC1=CC=C(C=C1)CC(=O)O)C(=O)OC(C)(C)C
InChI
InChI=1S/C34H54N4O10/c1-32(2,3)46-27(41)18-17-25(29(43)48-34(7,8)9)38-31(45)37-24(28(42)47-33(4,5)6)12-10-11-19-35-30(44)36-21-23-15-13-22(14-16-23)20-26(39)40/h13-16,24-25H,10-12,17-21H2,1-9H3,(H,39,40)(H2,35,36,44)(H2,37,38,45)/t24-,25-/m0/s1
InChIKey
IMNLHBFYVLUOKM-DQEYMECFSA-N

Boc-C2-Urea-bis(Boc)-C4-Urea-4-phenylacetic acid, a specialized compound utilized in diverse chemical and bioscience research arenas, is ripe with applications. Here are four key applications presented with high perplexity and burstiness:

Peptide Synthesis: Acting as a protective agent, Boc-C2-Urea-bis(Boc)-C4-Urea-4-phenylacetic acid plays a vital role in complex peptide synthesis. By safeguarding the amine groups throughout the synthesis process, it ensures reactions proceed smoothly, devoid of unwanted side reactions. This mechanism enables the creation of peptides with intricate sequences, crucial for cutting-edge biomedical research and pharmaceutical development.

Catalysis Research: A cornerstone in catalytic exploration, this compound functions as a pivotal reagent in innovating and researching new catalytic pathways, particularly in organic synthesis. It acts as a stabilizing force for catalytic intermediates, allowing for the exploration of more efficient and selective catalytic reactions. This role is paramount in propelling forward chemical manufacturing techniques and unveiling novel synthetic methodologies.

Drug Discovery: In the realm of drug development, Boc-C2-Urea-bis(Boc)-C4-Urea-4-phenylacetic acid assumes a pivotal role in synthesizing pharmaceutical intermediates and active pharmaceutical ingredients (APIs). Its incorporation into drug molecules enhances their stability, bioavailability, and target specificity. Researchers harness the power of this compound to craft and optimize lead compounds within the drug discovery pipeline, pushing the boundaries of pharmaceutical innovation.

Polymer Chemistry: A cornerstone in crafting novel polymers with bespoke properties, this compound integrates seamlessly into polymer architectures, enabling the creation of materials with specific mechanical, thermal, and chemical resistance profiles. These advanced polymers find applications across diverse sectors, including biomedical devices, coatings, and cutting-edge materials, showcasing the boundless potential of this compound in driving scientific innovation.

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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