Fmoc-Val-Cit-PAB - CAS 159858-22-7

Fmoc-Val-Cit-PAB - CAS 159858-22-7 Catalog number: BADC-00364

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Fmoc-Val-Cit-PAB is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs).

Category
ADCs Linker
Product Name
Fmoc-Val-Cit-PAB
CAS
159858-22-7
Catalog Number
BADC-00364
Molecular Formula
C33H39N5O6
Molecular Weight
601.70
Fmoc-Val-Cit-PAB

Ordering Information

Catalog Number Size Price Quantity
BADC-00364 100 mg $279 Inquiry
BADC-00364 10 g $299 Inquiry
BADC-00364 50 g $1299 Inquiry
Description
Fmoc-Val-Cit-PAB is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs).
Synonyms
Fmoc-Val-Cit-PAB-OH; L-Ornithinamide, N-[(9H-fluoren-9-ylmethoxy)carbonyl]-L-valyl-N5-(aminocarbonyl)-N-[4-(hydroxymethyl)phenyl]-
IUPAC Name
9H-fluoren-9-ylmethyl N-[(2S)-1-[[(2S)-5-(carbamoylamino)-1-[4-(hydroxymethyl)anilino]-1-oxopentan-2-yl]amino]-3-methyl-1-oxobutan-2-yl]carbamate
Canonical SMILES
CC(C)C(C(=O)NC(CCCNC(=O)N)C(=O)NC1=CC=C(C=C1)CO)NC(=O)OCC2C3=CC=CC=C3C4=CC=CC=C24
InChI
InChI=1S/C33H39N5O6/c1-20(2)29(38-33(43)44-19-27-25-10-5-3-8-23(25)24-9-4-6-11-26(24)27)31(41)37-28(12-7-17-35-32(34)42)30(40)36-22-15-13-21(18-39)14-16-22/h3-6,8-11,13-16,20,27-29,39H,7,12,17-19H2,1-2H3,(H,36,40)(H,37,41)(H,38,43)(H3,34,35,42)/t28-,29-/m0/s1
InChIKey
DALMAZHDNFCDRP-VMPREFPWSA-N
Density
1.276±0.06 g/cm3
Solubility
Soluble to 3200 mg/ml (5318 mm) in DMSO, not soluble in water
Melting Point
204 °C(dec.)
LogP
5.56000
PSA
171.88000
Appearance
White to Off-white Solid
Shelf Life
2 years
Shipping
Room temperature, or blue ice upon request.
Boiling Point
914.2±65.0 °C (Predicted)

Fmoc-Val-Cit-PAB, a chemical linker at the forefront of drug delivery and targeted therapy, boasts diverse applications. Here are four key uses:

Antibody-Drug Conjugates (ADCs): A vital element in ADC synthesis, Fmoc-Val-Cit-PAB plays a crucial role in delivering cytotoxic drugs specifically to cancer cells. This linker guarantees drug inactivity in circulation, only activating within target cells. Such precision minimizes off-target effects and enhances the therapeutic index of anticancer medications.

Targeted Prodrug Activation: Leveraging Fmoc-Val-Cit-PAB facilitates the creation of prodrugs with selective activation in specific tissues or cells. Through linker attachment to a prodrug, researchers ensure active drug release triggered by specific enzymatic activity in diseased tissues. This innovative strategy elevates drug efficacy while reducing systemic toxicity.

Peptide Drug Conjugation: In the realm of peptide-based drug design, Fmoc-Val-Cit-PAB acts as a stable linker for coupling therapeutic peptides to drug molecules or delivery systems. This linker provides chemical stability, enabling controlled peptide release in targeted environments. Such applications are pivotal in advancing peptide therapeutics and drug delivery systems.

Bioconjugation Studies: Employed in bioconjugation investigations, Fmoc-Val-Cit-PAB facilitates linking diverse biomolecules like peptides, proteins, and antibodies to other functional entities. Its use guarantees a stable and controlled connection between biomolecules and conjugated substances, fostering the creation of multifunctional bioconjugates for diagnostics, therapeutics, and research pursuits.

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: Fmoc-Val-Cit-PAB
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