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96640

Sigma-Aldrich

Z-Ile-ONp

≥98.0% (TLC)

Synonym(s):

Z-L-isoleucine 4-nitrophenyl ester

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About This Item

Empirical Formula (Hill Notation):
C20H22N2O6
CAS Number:
Molecular Weight:
386.40
Beilstein/REAXYS Number:
3176084
MDL number:
UNSPSC Code:
12352202
PubChem Substance ID:
NACRES:
NA.22
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assay

≥98.0% (TLC)

form

powder

reaction suitability

reaction type: solution phase peptide synthesis

application(s)

peptide synthesis

storage temp.

2-8°C

SMILES string

CC[C@H](C)[C@H](NC(=O)OCc1ccccc1)C(=O)Oc2ccc(cc2)[N+]([O-])=O

InChI

1S/C20H22N2O6/c1-3-14(2)18(21-20(24)27-13-15-7-5-4-6-8-15)19(23)28-17-11-9-16(10-12-17)22(25)26/h4-12,14,18H,3,13H2,1-2H3,(H,21,24)/t14-,18-/m0/s1

InChI key

NJDZCCJYUBNBMK-KSSFIOAISA-N

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable


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Rafael W Hartmann et al.
ChemMedChem, 15(24), 2500-2512 (2020-10-17)
Auristatins are a class of ultrapotent microtubule inhibitors, whose growing clinical popularity in oncology is based upon their use as payloads in antibody-drug conjugates (ADCs). The most widely utilized auristatin, MMAE, has however been shown to cause apoptosis in non-pathological

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