917184
BocA1V1PF2-OC10-NH2 hydrochloride
Manufacturer: Sigma Aldrich
Synonym(S): 10-Aminodecyl (S)-2-((S)-1-((S)-2-((S)-2-((tert-butoxycarbonyl)amino)propanamido)-3,3-dimethylbutanoyl)pyrrolidine-2-carboxamido)-3-(4-fluorophenyl)propanoate hydrochloride, AVP conjugate for IAP-mediated protein degrader development, SNIPER building block
Select a Size
| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| 50 MG | 917184-50-MG | In Stock | ₹ 36,837.48 |
917184 - 50 MG
In Stock
Quantity
1
Base Price: ₹ 36,837.48
GST (18%): ₹ 6,630.746
Total Price: ₹ 43,468.226
ligand
BocA1V1PF2
Quality Level
100
form
powder
reaction suitability
reactivity: carboxyl reactivereagent 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(OCCCCCCCCCCN)=O)CC2=CC=C(C=C2)F)=O)=O)C(C)(C)C)=O.Cl
Related Products
Description
- Application: Protein degrader building block BocA1V1PF2-OC10-NH2 hydrochloride 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 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:917478 BocA1V1PF2916927 BocA1V1PF2-OC6-NH2 hydrochloride917184 BocA1V1PF2-OC10-NH2 hydrochloride917435 BocA1V1PF2-OPEG1-NH2 hydrochloride917680 BocA1V1PF2-OPEG3-NH2 hydrochloride
- Other Notes: In Vivo Knockdown of Pathogenic Proteins via Specific and Nongenetic Inhibitor of Apoptosis Protein (IAP)-dependent Protein Erasers (SNIPERs)SNIPERs−Hijacking IAP activity to induce protein degradationE3 Ligase Ligands for PROTACs: How They Were Found and How to Discover New Ones
- Legal Information: PROTAC is a registered trademark of Arvinas Operations, Inc., and is used under license
SAFETY INFORMATION
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
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ligand: BocA1V1PF2
Quality Level: 100
form: powder
reaction suitability: reactivity: carboxyl reactivereagent 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(OCCCCCCCCCCN)=O)CC2=CC=C(C=C2)F)=O)=O)C(C)(C)C)=O.Cl
ligand:
BocA1V1PF2
Quality Level:
100
form:
powder
reaction suitability:
reactivity: carboxyl reactivereagent 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(OCCCCCCCCCCN)=O)CC2=CC=C(C=C2)F)=O)=O)C(C)(C)C)=O.Cl
ligand: __
Quality Level: 100
form: liquid
reaction suitability: reagent type: derivatization reagentreaction type: Acylationsreagent type: derivatization reagentreaction type: Esterifications
functional group: __
storage temp.: __
SMILES string: __
ligand:
__
Quality Level:
100
form:
liquid
reaction suitability:
reagent type: derivatization reagentreaction type: Acylationsreagent type: derivatization reagentreaction type: Esterifications
functional group:
__
storage temp.:
__
SMILES string:
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ligand: A1V2PF2
Quality Level: 100
form: crystals
reaction suitability: reactivity: carboxyl reactivereagent type: ligand-linker conjugate
functional group: amine
storage temp.: 2-8°C
SMILES string: C[C@H](NCCOCCOCCOCCN)C(N[C@H](C(N1CCC[C@H]1C(N[C@H](C(NCC)=O)CC2=CC=C(C=C2)F)=O)=O)C3CCCCC3)=O
ligand:
A1V2PF2
Quality Level:
100
form:
crystals
reaction suitability:
reactivity: carboxyl reactivereagent type: ligand-linker conjugate
functional group:
amine
storage temp.:
2-8°C
SMILES string:
C[C@H](NCCOCCOCCOCCN)C(N[C@H](C(N1CCC[C@H]1C(N[C@H](C(NCC)=O)CC2=CC=C(C=C2)F)=O)=O)C3CCCCC3)=O
ligand: __
Quality Level: __
form: __
reaction suitability: __
functional group: __
storage temp.: __
SMILES string: __
ligand:
__
Quality Level:
__
form:
__
reaction suitability:
__
functional group:
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storage temp.:
__
SMILES string:
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