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

H-L-Ser(Propargyl)-OH hydrochloride

  CAS No.: 1379006-45-7   Cat No.: BADC-01718 4.5  

H-L-Ser(Propargyl)-OH hydrochloride is a serine-based ADC linker building block featuring a propargyl group for site-selective click conjugation. It improves antibody-drug conjugate stability and targeted payload delivery efficiency. Keywords: ADC linker, propargyl linker, serine derivative, click chemistry, bioconjugation.

H-L-Ser(Propargyl)-OH hydrochloride

Structure of 1379006-45-7

Quality
Assurance

Worldwide
Delivery

24/7 Customer
Support
Category
ADC Linker
Molecular Formula
C6H10ClNO3
Molecular Weight
179.60

* 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
H-L-Ser(Propargyl)-OH (hydrochloride)
IUPAC Name
(2S)-2-amino-3-prop-2-ynoxypropanoic acid;hydrochloride
Canonical SMILES
C#CCOCC(C(=O)O)N.Cl
InChI
InChI=1S/C6H9NO3.ClH/c1-2-3-10-4-5(7)6(8)9;/h1,5H,3-4,7H2,(H,8,9);1H/t5-;/m0./s1
InChIKey
MWOGTBHNDWZTLL-JEDNCBNOSA-N

H-L-Ser(Propargyl)-OH hydrochloride, a versatile chemical compound utilized in peptidomimetics and drug design, boasts a diverse range of applications in bioscience. Here are four key applications:

Peptide Synthesis: H-L-Ser(Propargyl)-OH hydrochloride contributes to the synthesis of peptides adorned with terminal alkyne groups, facilitating click chemistry reactions. This innovative approach empowers researchers to construct intricate peptide structures with unparalleled efficiency. These tailored peptides find utility in investigations pertaining to protein interactions and functionality, offering a window into the intricate web of molecular biology.

Drug Development: H-L-Ser(Propargyl)-OH hydrochloride acts as a fundamental building block in the creation of novel compounds with promising therapeutic potentials. Its integration into peptidomimetics elevates the stability and binding affinity of lead compounds, paving the way for the development of next-generation drugs with enhanced pharmacokinetic attributes.

Chemical Biology: A linchpin in the domain of chemical biology, H-L-Ser(Propargyl)-OH hydrochloride finds application in studying post-translational modifications of proteins. By introducing alkyne handles, researchers can selectively label and monitor specific proteins within live cellular environments. This technique offers a unique insight into the dynamic nature and functional intricacies of proteins within their biological milieu.

Bioorthogonal Chemistry: The alkyne moiety within H-L-Ser(Propargyl)-OH hydrochloride stands as a critical tool in the toolbox of bioorthogonal chemistry, empowering researchers to modify biomolecules covalently without disrupting native cellular processes. This strategic capability opens avenues for precise imaging and probing of biological systems in a highly selective and efficient manner.

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 Linker Development Enzyme Cleavable Linker Cathepsin B Cleavable Linker/Peptide Linker Phosphatase Cleavable Linker β-Glucuronide Linker β-Galactosidase Cleavable Linker Sulfatase Cleavable Linker Chemically Cleavable Linker Non-Cleavable Linker Services Acid Cleavable Linker/Hydrazone Linker

Unlock Deeper ADC Insights

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

Linkers - A Crucial Factor in Antibody–Drug Conjugates In-Depth Review of ADC Linkers: Types, Mechanisms, and Research Progress New Structural Insights Solve Instability Issues of Maleimide Linkers in ADCs PEG Linkers in Antibody-Drug Conjugates Peptide Linkers in Antibody-Drug Conjugates Disulfide Linkers in Antibody-Drug Conjugates Biotinylation Reagents in Antibody-Drug Conjugates Maleimide Linkers in Antibody-Drug Conjugates Current ADC Linker Chemistry SPDB Linkers in Antibody-Drug Conjugates

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: Mal-PEG4-PFP | Azide-C2-SS-C2-biotin | 4-Maleimidobutyric acid | MC-Gly-Gly-{D-Phe}-Gly-NH-CH2-O-CH2COOH | Boc-L-Tyr(2-azidoethyl)-OH | Dov-Val-Dil-OH TFA | Dov-Val-Dil-OH | H-L-Lys(N3-Gly)-OH | H-D-Tyr(Propargyl)-OH | Boc-C2-Urea-bis(Boc)-C4-Urea-4-phenylacetic acid | H-L-Ser(Propargyl)-OH hydrochloride
Send Inquiry
Verification code
Inquiry Basket