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Merck
CN

936421

Fmoc-Val-Ala-OH

≥95%

Synonym(s):

N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-L-valyl-L-alanine, L-Alanine, N-[(9H-fluoren-9-ylmethoxy)carbonyl]-L-valyl-, L-Alanine, N-[N-[(9H-fluoren-9-ylmethoxy)carbonyl]-L-valyl]-

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About This Item

Empirical Formula (Hill Notation):
C23H26N2O5
Molecular Weight:
410.46
UNSPSC Code:
12352106
NACRES:
NA.22
MDL number:
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InChI key

KQZMZNLKVKGMJS-XOBRGWDASA-N

SMILES string

C(OC(N[C@H](C(N[C@H](C(O)=O)C)=O)C(C)C)=O)C1C=2C(C=3C1=CC=CC3)=CC=CC2

InChI

1S/C26H32N4O6/c1-15(2)22(23(31)29-21(24(32)33)12-7-13-28-25(27)34)30-26(35)36-14-20-18-10-5-3-8-16(18)17-9-4-6-11-19(17)20/h3-6,8-11,15,20-22H,7,12-14H2,1-2H3,(H,29,31)(H,30,35)(H,32,33)(H3,27,28,34)/t21-,22-/m0/s1

assay

≥95%

form

powder or crystals

color

white to off-white

storage temp.

2-8°C

Quality Level

Application

Fmoc-Val-Ala-OH is a lysosomally cleavable linker used in construction of antibody-drug conjugates (ADC & Bioconjugation).

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

Regulatory Information

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Alain Beck et al.
Nature reviews. Drug discovery, 16(5), 315-337 (2017-03-18)
Antibody-drug conjugates (ADCs) are one of the fastest growing classes of oncology therapeutics. After half a century of research, the approvals of brentuximab vedotin (in 2011) and trastuzumab emtansine (in 2013) have paved the way for ongoing clinical trials that

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