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

Fmoc-Gly-Gly-D-Phe-OH

  CAS No.:   Cat No.: BADC-01261   Purity: 98.0% 4.5  

Fmoc-Gly-Gly-D-Phe-OH is a D-amino acid peptide ADC linker intermediate facilitating protease-sensitive, site-specific antibody conjugation for enhanced stability and targeted payload delivery in antibody-drug conjugates.

Fmoc-Gly-Gly-D-Phe-OH

Structure of

Quality
Assurance

Worldwide
Delivery

24/7 Customer
Support
Category
ADC Linker
Molecular Formula
C28H27N3O6
Molecular Weight
501.53
Shipping
Room temperature
Shipping
Store at -20 °C, keep in dry and avoid sunlight.

* 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
Solubility
10 mm in DMSO
Shelf Life
0-4°C for short term (days to weeks), or -20°C for long term (months).
Shipping
Room temperature
Storage
Store at -20 °C, keep in dry and avoid sunlight.

Fmoc-Gly-Gly-D-Phe-OH, a versatile peptide synthesis reagent utilized in the fields of biochemistry and molecular biology, boasts diverse applications. Here are four key applications:

Peptide Synthesis: Serving as a fundamental component in solid-phase peptide synthesis (SPPS), Fmoc-Gly-Gly-D-Phe-OH acts as a crucial building block. Its Fmoc protective group ensures stability throughout the chain elongation process, enabling the precise construction of intricate peptide sequences. This method facilitates the generation of highly purified peptides tailored for both research purposes and therapeutic applications.

Drug Development: In the realm of drug discovery, Fmoc-Gly-Gly-D-Phe-OH plays a pivotal role in synthesizing peptide-based drug candidates. These peptides can mimic crucial protein-protein interactions or regulate biological pathways, offering innovative therapeutic avenues for combating diseases like cancer, diabetes, and infectious ailments. Custom peptides synthesized using Fmoc-Gly-Gly-D-Phe-OH can be fine-tuned for enhanced potency, selectivity, and stability, propelling pharmaceutical advancements.

Structural Biology: Researchers harness the power of Fmoc-Gly-Gly-D-Phe-OH to fabricate peptide probes and models essential for investigating protein structure and function. These synthetic peptides find utility in techniques such as X-ray crystallography and NMR spectroscopy, aiding in the comprehensive exploration of protein folding and intermolecular interactions. Understanding these intricate structural nuances is imperative for informed drug design strategies and innovative protein engineering endeavors.

Bioconjugation: Functioning as a versatile linker or spacer, Fmoc-Gly-Gly-D-Phe-OH contributes to the creation of bioconjugates where peptides are conjugated to diverse molecules like drugs, fluorophores, or antibodies. This bioconjugation process is indispensable for crafting advanced diagnostic tools and targeted therapies. The presence of D-Phe enhances the stability and bioavailability of the conjugated peptides in clinical and research settings.

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: Azido-C6-OH | Amino-PEG2-t-butyl ester | Mal-PEG4-VC-PAB-DMEA-Seco-Duocarmycin SA | NHPI-PEG2-C2-PFP ester | 1,6-Bis(mesyloxy)hexane | Cys-mcMMAD | Lys-SMCC-DM1 | MC-Val-Cit-PAB-clindamycin | DC1 | Boc-D-trans-Hyp-Ome | Fmoc-Gly-Gly-D-Phe-OH
Send Inquiry
Verification code
Inquiry Basket