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916706

BocA1V2PF1-NHC10-NH2

Synonyma:

tert-Butyl ((S)-1-(((S)-2-((S)-2-(((S)-1-((10-aminodecyl)amino)-1-oxo-3-phenylpropan-2-yl)carbamoyl)pyrrolidin-1-yl)-1-cyclohexyl-2-oxoethyl)amino)-1-oxopropan-2-yl)carbamate, AVP conjugate for IAP-mediated protein degrader development, SNIPER building block

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Vybrat velikost

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Vám/Skladová položkaDostupnostCena
50 mg
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11 700,00 Kč

O této položce

Empirický vzorec (Hillův zápis):
C40H66N6O6
Molekulová hmotnost:
726.99
MDL number:
UNSPSC Code:
41116105
NACRES:
NA.22

11 700,00 Kč


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ligand

BocA1V2PF1

Quality Segment

form

powder, crystals or chunks

reaction suitability

reactivity: carboxyl reactive, reagent type: ligand-linker conjugate

functional group

amine

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(NCCCCCCCCCCN)=O)CC2=CC=CC=C2)=O)=O)C3CCCCC3)=O

InChI

1S/C40H66N6O6/c1-29(43-39(51)52-40(2,3)4)35(47)45-34(31-22-15-12-16-23-31)38(50)46-27-19-24-33(46)37(49)44-32(28-30-20-13-11-14-21-30)36(48)42-26-18-10-8-6-5-7-9-17-25-41/h11,13-14,20-21,29,31-34H,5-10,12,15-19,22-28,41H2,1-4H3,(H,42,48)(H,43,51)(H,44,49)

InChI key

DWWHKOSRCMFTCZ-UYDQTSAYSA-N

Application

Protein degrader building block BocA1V2PF1-NHC10-NH2 enables the synthesis of molecules for targeted protein degradation and SNIPER (specific and non-genetic inhibitor of apoptosis protein (IAP)-dependent protein erasers) technology. Developed in partnership with ComInnex, this conjugate contains an in silico-derived IAP-recruiting ligand, an alkyl-chain crosslinker, and a pendant amine for reactivity with an acid on a target warhead. Because even slight alterations in ligands and crosslinkers can affect ternary complex formation between the target, E3 ligase, and protein degrader, many analogs are prepared to screen for optimal target degradation. When used with other protein degrader building blocks with a terminal amine, including CRBN and VHL targeted, parallel synthesis can be used to more quickly generate SNIPER and PROTAC® degrader libraries that feature variation in crosslinker length, composition, and E3 ligase ligand. Learn more about the novel IAP ligands generated through virtual screening of AVP mimetics in our Technology Spotlight.

Building blocks in this series:
916978 BocA1V2PF1
917966 BocA1V2PF1-NHC6-NH2
916706 BocA1V2PF1-NHC10-NH2
916951 BocA1V2PF1-NHPEG1-NH2
917214 BocA1V2PF1-NHPEG3-NH2

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

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Tato položka
917443916692917966
description

-

description

-

description

≥95%

description

-

reaction suitability

reactivity: carboxyl reactive, reagent type: ligand-linker conjugate

reaction suitability

reactivity: carboxyl reactive, reagent type: ligand-linker conjugate

reaction suitability

reactivity: carboxyl reactive, reagent type: ligand-linker conjugate

reaction suitability

reactivity: carboxyl reactive, reagent type: ligand-linker conjugate

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, crystals or chunks

form

powder

form

powder

form

powder

ligand

BocA1V2PF1

ligand

BocA1V2PF2

ligand

BocA1V2PF2

ligand

BocA1V2PF1

functional group

amine

functional group

amine

functional group

amine

functional group

amine


Skladovací třída

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable



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Lot/Batch Number

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