Fmoc-3VVD-OH - CAS 863971-44-2

Fmoc-3VVD-OH - CAS 863971-44-2 Catalog number: BADC-00695

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Fmoc-3VVD-OH is a cleavable ADC linker used to synthesize antibody-drug conjugations (ADCs).

Category
ADCs Linker
Product Name
Fmoc-3VVD-OH
CAS
863971-44-2
Catalog Number
BADC-00695
Molecular Formula
C36H51N3O7
Molecular Weight
637.81
Fmoc-3VVD-OH

Ordering Information

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BADC-00695 -- $--
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Description
Fmoc-3VVD-OH is a cleavable ADC linker used to synthesize antibody-drug conjugations (ADCs).
Synonyms
(5S,9S,11S,12R)-11-((S)-sec-butyl)-1-(9H-fluoren-9-yl)-5,9-diisopropyl-12-methoxy-4,10-dimethyl-3,6,8-trioxo-2-oxa-4,7,10-triazatetradecan-14-oic acid; N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-N-methyl-L-valyl-N-[(2R,3S,4S)-1-carboxy-2-methoxy-4-methyl-3-hexanyl]-N-methyl-L-valinamide; L-Valinamide, N-[(9H-fluoren-9-ylmethoxy)carbonyl]-N-methyl-L-valyl-N-[(1S,2S)-1-[(1R)-2-carboxy-1-methoxyethyl]-2-methylbutyl]-N-methyl-; FMOC-3AA-OH
IUPAC Name
(3R,4S,5S)-4-[[(2S)-2-[[(2S)-2-[9H-fluoren-9-ylmethoxycarbonyl(methyl)amino]-3-methylbutanoyl]amino]-3-methylbutanoyl]-methylamino]-3-methoxy-5-methylheptanoic acid
Canonical SMILES
CCC(C)C(C(CC(=O)O)OC)N(C)C(=O)C(C(C)C)NC(=O)C(C(C)C)N(C)C(=O)OCC1C2=CC=CC=C2C3=CC=CC=C13
InChI
InChI=1S/C36H51N3O7/c1-10-23(6)33(29(45-9)19-30(40)41)38(7)35(43)31(21(2)3)37-34(42)32(22(4)5)39(8)36(44)46-20-28-26-17-13-11-15-24(26)25-16-12-14-18-27(25)28/h11-18,21-23,28-29,31-33H,10,19-20H2,1-9H3,(H,37,42)(H,40,41)/t23-,29+,31-,32-,33-/m0/s1
InChIKey
SMVBIYSFDNRJJI-FCUBIXSHSA-N
Density
1.1±0.1 g/cm3
Solubility
Soluble in DMSO
Purity
≥95%
Shipping
Room temperature
Storage
Store at 2-8°C, stored under nitrogen
Boiling Point
793.0±60.0°C at 760 mmHg

Fmoc-3VVD-OH, a fluorenylmethyloxycarbonyl (Fmoc) protected amino acid derivative, plays a pivotal role in peptide synthesis and biochemical research. Here are four key applications of Fmoc-3VVD-OH:

Peptide Synthesis: Essential in solid-phase peptide synthesis (SPPS), Fmoc-3VVD-OH facilitates the precise assembly of intricate peptide chains. The Fmoc group shields the amino terminal, safeguarding against undesirable reactions during synthesis. This meticulous process ensures the synthesis of peptides with pristine purity and accuracy, critical for a myriad of biochemical and pharmaceutical investigations.

Drug Development: Leveraging Fmoc-3VVD-OH within peptide libraries is instrumental in the exploration of novel therapeutic peptides possessing drug-like attributes. Researchers can design and evaluate diverse peptide sequences to screen for biological activity, binding affinity, and stability. This methodology expedites the identification and refinement of peptide-based drugs aimed at combating various diseases,.

Protein Engineering: In the realm of protein engineering, Fmoc-3VVD-OH is deployed to craft modified peptides and proteins endowed with distinctive properties and functions. By integrating this specific amino acid derivative into protein sequences, researchers introduce a spectrum of structural and functional diversity. These tailored proteins serve as invaluable tools for probing protein interactions, stability, and functionality across diverse biological contexts, enriching our understanding of protein behavior.

Bioconjugation: Fmoc-3VVD-OH plays a pivotal role in the development of peptide conjugates that link peptides to other molecules like drugs, probes, or nanoparticles. This conjugation enhances the specificity, delivery, and efficacy of therapeutic agents and diagnostic tools. Bioconjugates formulated with Fmoc-3VVD-OH find application in targeted drug delivery, imaging techniques, and biosensor technologies.

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: PDB-Pfp | Fmoc-3VVD-OH
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