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917478

Sigma-Aldrich

BocA1V1PF2

≥95%

Synonym(s):

(S)-2-((S)-1-((S)-2-((S)-2-((tert-Butoxycarbonyl)amino)propanamido)-3,3-dimethylbutanoyl)pyrrolidine-2-carboxamido)-3-(4-fluorophenyl)propanoic acid, AVP ligand, IAP E3 ligase lead for protein degrader research, SNIPER building block

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100 MG
$539.00

About This Item

Empirical Formula (Hill Notation):
C28H41FN4O7
Molecular Weight:
564.65
MDL number:
UNSPSC Code:
41116105
NACRES:
NA.22

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$539.00


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ligand

BocA1V1PF2

Quality Level

assay

≥95%

form

powder

reaction suitability

reagent type: ligand

functional group

carboxylic acid

storage temp.

2-8°C

SMILES string

C[C@H](NC(OC(C)(C)C)=O)C(N[C@H](C(N1CCC[C@H]1C(N[C@H](C(O)=O)CC2=CC=C(C=C2)F)=O)=O)C(C)(C)C)=O

InChI

1S/C28H41FN4O7/c1-16(30-26(39)40-28(5,6)7)22(34)32-21(27(2,3)4)24(36)33-14-8-9-20(33)23(35)31-19(25(37)38)15-17-10-12-18(29)13-11-17/h10-13,16,19-21H,8-9,14-15H2,1-7H3,(H,30,39)(H,31,35)(H,32,34)(H,37,38)/t16-,19-,20-,21+/m0/s1

InChI key

JVBWBZOMRINKPT-LRGNLBRXSA-N

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This Item
916978917974917710
assay

≥95%

assay

≥95%

assay

-

assay

≥95%

functional group

carboxylic acid

functional group

carboxylic acid

functional group

carboxylic acid

functional group

amine

reaction suitability

reagent type: ligand

reaction suitability

reagent type: ligand

reaction suitability

reagent type: ligand

reaction suitability

reagent type: ligand

Quality Level

100

Quality Level

100

Quality Level

100

Quality Level

100

storage temp.

2-8°C

storage temp.

2-8°C

storage temp.

2-8°C

storage temp.

2-8°C

form

powder

form

powder

form

powder

form

powder

Application

BocA1V1PF2 is an in silico-derived inhibitor of apoptosis protein (IAP)-recruiting ligand for targeted protein degradation and SNIPER (specific and non-genetic IAP-dependent protein erasers) development, launched in partnership with ComInnex. Learn more about the novel IAP ligands generated through virtual screening of AVP mimetics in our Technology Spotlight. A C-terminal variant of BocA1V1PF2 is also available as A1V1PF2-OEt (917710).

BocA1V1PF2 conjugates are also available for degrader synthesis. Browse our full synthesis offering here for streamlining SNIPER and PROTAC® degrader libraries: Degrader Building Blocks
916927 BocA1V1PF2-OC6-NH2 hydrochloride
917184 BocA1V1PF2-OC10-NH2 hydrochloride
917435 BocA1V1PF2-OPEG1-NH2 hydrochloride
917680 BocA1V1PF2-OPEG3-NH2 hydrochloride

Technology Spotlight: Degrader Building Blocks with Inhibitor of Apoptosis Protein (IAP) In Silico-Derived Ligands

Legal Information

PROTAC is a registered trademark of Arvinas Operations, Inc., and is used under license

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable


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