Boc-D-trans-Hyp-OH - CAS 147266-92-0

Boc-D-trans-Hyp-OH - CAS 147266-92-0 Catalog number: BADC-01919

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Boc-D-trans-Hyp-OH is a non-cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs). It is also an alkyl chain-based PROTAC linker that can be used in the synthesis of PROTACs.

Category
ADCs Linker
Product Name
Boc-D-trans-Hyp-OH
CAS
147266-92-0
Catalog Number
BADC-01919
Molecular Formula
C10H17NO5
Molecular Weight
231.25
Boc-D-trans-Hyp-OH

Ordering Information

Catalog Number Size Price Quantity
BADC-01919 -- $--
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Description
Boc-D-trans-Hyp-OH is a non-cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs). It is also an alkyl chain-based PROTAC linker that can be used in the synthesis of PROTACs.
Synonyms
(2R,4S)-1-(tert-butoxycarbonyl)-4-hydroxypyrrolidine-2-carboxylic acid; N-Boc-trans-4-hydroxy-d-proline
IUPAC Name
(2R,4S)-4-hydroxy-1-[(2-methylpropan-2-yl)oxycarbonyl]pyrrolidine-2-carboxylic acid
Canonical SMILES
CC(C)(C)OC(=O)N1CC(CC1C(=O)O)O
InChI
InChI=1S/C10H17NO5/c1-10(2,3)16-9(15)11-5-6(12)4-7(11)8(13)14/h6-7,12H,4-5H2,1-3H3,(H,13,14)/t6-,7+/m0/s1
InChIKey
BENKAPCDIOILGV-NKWVEPMBSA-N
Density
1.312±0.06 g/cm3
Melting Point
123°C
Purity
≥ 97%
Boiling Point
390.9±42.0°C

Boc-D-trans-Hyp-OH, a derivative of hydroxyproline utilized in peptide synthesis and drug development, boasts a multitude of applications. Here are four key applications expressed with a high degree of perplexity and burstiness:

Peptide Synthesis: Serving as a cornerstone in cyclic peptides and peptidomimetics synthesis, Boc-D-trans-Hyp-OH elevates stability and biological activity within peptide chains. This enhancement is paramount for the creation of peptide-based drugs and therapeutic agents, propelling advancements in medical treatments.

Collagen Research: Delving into the intricacies of collagen’s structure and function, Boc-D-trans-Hyp-OH stands as a pivotal player in collagen exploration. As hydroxyproline forms an integral part of collagen, its derivatives aid in crafting collagen-like peptides for in-depth structural investigations, shedding light on collagen-related ailments like osteogenesis imperfecta.

Drug Development: Spearheading the design and synthesis of proline-rich peptides for therapeutic applications, Boc-D-trans-Hyp-OH is a driving force in drug development. These peptides often exhibit enhanced pharmacokinetics and bioavailability, offering promising avenues for drug discovery. Through the integration of Boc-D-trans-Hyp-OH, researchers can forge potent and targeted drug candidates with increased efficacy.

Structural Biology: In the realm of structural biology, Boc-D-trans-Hyp-OH serves as a linchpin for unraveling the influence of hydroxyproline on protein folding and stability. By replacing natural amino acids with Boc-D-trans-Hyp-OH, scientists delve into the dynamics and interactions of proteins, illuminating the mechanisms underlying protein-related diseases. This profound grasp of protein behavior is essential for therapeutic protein development and combating complex diseases.

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

Historical Records: Boc-D-trans-Hyp-OH
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