Structure Info
- Chemspace ID
- CSSS00161189048 (In-Stock Screening Compounds)
- CAS
- 2230821-27-7
- MFCD
- MFCD32062811
- IUPAC Name
- (2S,4R)-1-[(2S)-2-[3-(2-{[5-({4-[(3-chloro-4-fluorophenyl)amino]-7-methoxyquinazolin-6-yl}oxy)pentyl]oxy}ethoxy)propanamido]-3,3-dimethylbutanoyl]-4-hydroxy-N-{[4-(4-methyl-1,3-thiazol-5-yl)phenyl]methyl}pyrrolidine-2-carboxamide
- Mol formula
- C47H57ClFN7O8S
- Mol weight
- 935 Da
- Catalog Number(s)
- 28597, 198574, A346407, AA01JK4G, ACS-2952, AG01JK78, AR01JKW8, AZ92060, BD00774997, BH92060, BISN0057, BP-28379, CS-0087480, CSC161189048, D80333, F986380, FPD82127, G223000, HY-123921, LAN-B67889, T5437, Y1012751
- Zoom the structure
- CSSS00161189048
Items Overall 16 items from 3 suppliers
Supplier | Lead time | Ships from | Purity | Pack | Price, € | Qty |
---|---|---|---|---|---|---|
MedChemExpress | 10 days | United States To: | 99 | 5 mg | 129 | |
MedChemExpress | 10 days | United States To: | 99 | 100 mg | 750 | |
Description: Names: Gefitinib-based PROTAC 3; Product Description: Gefitinib-based PROTAC 3, conjugating an EGFR binding element to a von Hippel-Lindau ligand via a linker, induces EGFR degradation with DC 50 s of 11.7 nM and 22.3 nM in HCC827(exon 19 del) and H3255 (L858R mutantion) cells, respectively .; Target: EGFR;PROTACs; CAS: 2230821-27-7 | ||||||
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MedChemExpress EU | 10 days | Sweden To: | 99 | 5 mg | 136 | |
MedChemExpress EU | 10 days | Sweden To: | 99 | 100 mg | 790 | |
Description: Names: Gefitinib-based PROTAC 3; Product Description: Gefitinib-based PROTAC 3, conjugating an EGFR binding element to a von Hippel-Lindau ligand via a linker, induces EGFR degradation with DC50s of 11.7 nM and 22.3 nM in HCC827(exon 19 del) and H3255 (L858R mutantion) cells, respectively; Target: EGFR;PROTACs; CAS: 2230821-27-7 | ||||||
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Targetmol Chemicals Inc | 30 days | United States To: | 97 | 2 mg | 38 | |
Targetmol Chemicals Inc | 30 days | United States To: | 97 | 100 mg | 393 | |
Description: Gefitinib-based PROTAC 3, which connects an EGFR binding element to a VHL ligand via a linker, induces EGFR degradation with DC50s of 11.7 nM and 22.3 nM in HCC827 (exon 19 del) and H3255 (L858R mutation) cells, respectively[1].; CAS: 2230821-27-7 | ||||||
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