Pomalidomide-C6-NH2?hydrochloride
Pomalidomide-C6-NH2?hydrochloride Basic information
- Product Name:
- Pomalidomide-C6-NH2?hydrochloride
- Synonyms:
-
- Pomalidomide-C6-NH2?hydrochloride
- 4-((6-aminohexyl)amino)-2-(2,6-dioxopiperidin-3-yl)isoindoline-1,3-dione
- Thalidomide-NH-C6-NH2 HCl
- Thalidomide-NH-C6-NH2 hydrochloride
- E3 Ligase Ligand-Linker Conjugates,inhibit,Thalidomide-NH-C-6-NH2 hydrochloride,ThalidomideNHC6NH2 hydrochloride,Thalidomide NH C6 NH2 hydrochloride,Inhibitor
- 4-((6-Aminohexyl)amino)-2-(2,6-dioxopiperidin-3-yl)isoindoline-1,3-dione hydrochloride, Crosslinker?E3 ligase ligand conjugate, Pomalidomide conjugate, Protein degrader building block for PROTAC? research, Template for synthesis of targeted protein degrader
- Poma-C6-NH2·HCl
- Pomalidomide 4'-alkylC6-amine
- CAS:
- 2375194-37-7
- MF:
- C19H25ClN4O4
- MW:
- 408.88
- Mol File:
- 2375194-37-7.mol
Pomalidomide-C6-NH2?hydrochloride Chemical Properties
- storage temp.
- 2-8°C
- solubility
- DMSO: Soluble
Methanol: Soluble - form
- Solid
- color
- Light yellow to yellow
- InChI
- 1S/C19H24N4O4.ClH/c20-10-3-1-2-4-11-21-13-7-5-6-12-16(13)19(27)23(18(12)26)14-8-9-15(24)22-17(14)25;/h5-7,14,21H,1-4,8-11,20H2,(H,22,24,25);1H
- InChIKey
- PBGMRXNTLPSDNR-UHFFFAOYSA-N
- SMILES
- O=C(C(CC1)N(C2=O)C(C3=C2C=CC=C3NCCCCCCN)=O)NC1=O.Cl
Pomalidomide-C6-NH2?hydrochloride Usage And Synthesis
Uses
Thalidomide-NH-C6-NH2 hydrochloride is a synthesized E3 ligase ligand-linker conjugate that incorporates the Thalidomide based cereblon ligand and a linker used in PROTAC technology[1].
reaction suitability
reactivity: carboxyl reactive
reagent type: ligand-linker conjugate
IC 50
Cereblon
References
[1] Sato T, et al. Cereblon-Based Small-Molecule Compounds to Control Neural Stem Cell Proliferation in Regenerative Medicine.?Front Cell Dev Biol. 2021;9:629326. Published 2021 Mar 11. DOI:10.3389/fcell.2021.629326
[2] Nalawansha DA, et al. PROTACs: An Emerging Therapeutic Modality in Precision Medicine. Cell Chem Biol. 2020;27(8):998-985. DOI:10.7554/eLife.57277
[3] ZHIQIANG SUN . Discovery of pomalidomide-based PROTACs for selective degradation of histone deacetylase 8[J]. European Journal of Medicinal Chemistry, 2022, 239: Article 114544. DOI: 10.1016/j.ejmech.2022.114544
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Pomalidomide-C6-NH2?hydrochloride(2375194-37-7)Related Product Information
- E3 ligase Ligand-Linker Conjugates 49
- Pomalidomide-C6-PEG1-C3-PEG1-butyl iodide
- Pomalidomide-C6-PEG3-butyl iodide
- E3 ligase Ligand-Linker Conjugates 55
- 1H-Isoindole-1,3(2H)-dione, 4-[(2-aminoethyl)amino]-2-(2,6-dioxo-3-piperidinyl)-, hydrochloride (1:1)
- Pomalidomide-6-2-2-6-N3
- Pomalidomide-amido-C1-Br
- Nonanoic acid, 9-[[2-(2,6-dioxo-3-piperidinyl)-2,3-dihydro-1,3-dioxo-1H-isoindol-4-yl]amino]-
- Octanoic acid, 8-[[2-(2,6-dioxo-3-piperidinyl)-2,3-dihydro-1,3-dioxo-1H-isoindol-4-yl]amino]-
- 4-[(8-Aminooctyl)amino]-2-(2,6-dioxopiperidin-3-yl)isoindoline-1,3-dione HCl
- POMALIDOMIDE-C9-CO2H
- Butanoic acid, 4-[[2-(2,6-dioxo-3-piperidinyl)-2,3-dihydro-1,3-dioxo-1H-isoindol-4-yl]amino]-
- 4-[(2-Aminoethyl)amino]-2-(2,6-dioxopiperidin-3-yl)isoindoline-1,3-dione HCl
- Pomalidomide-C3-NH2
- Heptanoic acid, 7-[[2-(2,6-dioxo-3-piperidinyl)-2,3-dihydro-1,3-dioxo-1H-isoindol-4-yl]amino]-
- Pomalidomide 4'-alkylC5-acid
- 4-[(4-Aminobutyl)amino]-2-(2,6-dioxopiperidin-3-yl)isoindoline-1,3-dione HCl
- β-Alanine, N-[2-(2,6-dioxo-3-piperidinyl)-2,3-dihydro-1,3-dioxo-1H-isoindol-4-yl]-