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R658947-100mg
(R)-BAY-899 (C09-1167-993)
Price: $1,278.12List Price: $1,420.14(R)-BAY-899 is the R-enantiomer of BAY-899. BAY-899 is an orally active and selective luteinizing hormone receptor (LH-R) antagonist with IC50s of 185 nM and 46nM for hLH (human LH) and rLH (rat LH), respectively.Appearance:SolidBiological -
R658947-10mg
(R)-BAY-899 (C09-1167-994)
Price: $306.46List Price: $340.51(R)-BAY-899 is the R-enantiomer of BAY-899. BAY-899 is an orally active and selective luteinizing hormone receptor (LH-R) antagonist with IC50s of 185 nM and 46nM for hLH (human LH) and rLH (rat LH), respectively.Appearance:SolidBiological -
R658947-25mg
(R)-BAY-899 (C09-1167-995)
Price: $518.18List Price: $575.75(R)-BAY-899 is the R-enantiomer of BAY-899. BAY-899 is an orally active and selective luteinizing hormone receptor (LH-R) antagonist with IC50s of 185 nM and 46nM for hLH (human LH) and rLH (rat LH), respectively.Appearance:SolidBiological -
R658947-50mg
(R)-BAY-899 (C09-1167-996)
Price: $779.47List Price: $866.08(R)-BAY-899 is the R-enantiomer of BAY-899. BAY-899 is an orally active and selective luteinizing hormone receptor (LH-R) antagonist with IC50s of 185 nM and 46nM for hLH (human LH) and rLH (rat LH), respectively.Appearance:SolidBiological -
R658947-5mg
(R)-BAY-899 (C09-1167-997)
Price: $191.94List Price: $213.27(R)-BAY-899 is the R-enantiomer of BAY-899. BAY-899 is an orally active and selective luteinizing hormone receptor (LH-R) antagonist with IC50s of 185 nM and 46nM for hLH (human LH) and rLH (rat LH), respectively.Appearance:SolidBiological -
R658774-10mg
(rel)-PROTAC ERRα Degrader-1 (C09-1167-985)
Price: $1,825.42List Price: $2,028.24(rel)-PROTAC ERRα Degrader-1 is a relative configuration of PROTAC ERRα Degrader-1. PROTAC ERRα Degrader-1 comprises a MDM2 ligand binding group, a linker and an estrogen-related receptor alpha ( ERRa ) binding group. PROTAC ERRα Degrader-1 is an -
R658774-1mg
(rel)-PROTAC ERRα Degrader-1 (C09-1167-986)
Price: $670.01List Price: $744.46(rel)-PROTAC ERRα Degrader-1 is a relative configuration of PROTAC ERRα Degrader-1. PROTAC ERRα Degrader-1 comprises a MDM2 ligand binding group, a linker and an estrogen-related receptor alpha ( ERRa ) binding group. PROTAC ERRα Degrader-1 is an -
R658774-5mg
(rel)-PROTAC ERRα Degrader-1 (C09-1167-987)
Price: $1,192.99List Price: $1,325.54(rel)-PROTAC ERRα Degrader-1 is a relative configuration of PROTAC ERRα Degrader-1. PROTAC ERRα Degrader-1 comprises a MDM2 ligand binding group, a linker and an estrogen-related receptor alpha ( ERRa ) binding group. PROTAC ERRα Degrader-1 is an -
18119-1
(S)-PFI-2 (hydrochloride)-1 mg
Price: $105.41List Price: $117.12The inactive enantiomer of the SET7/9 inhibitor (R)-PFI-2 that may serve as a negative control. -
18119-10
(S)-PFI-2 (hydrochloride)-10 mg
Price: $415.73List Price: $461.92The inactive enantiomer of the SET7/9 inhibitor (R)-PFI-2 that may serve as a negative control. -
18119-5
(S)-PFI-2 (hydrochloride)-5 mg
Price: $269.99List Price: $299.98The inactive enantiomer of the SET7/9 inhibitor (R)-PFI-2 that may serve as a negative control. -
H7904-25MG
(Z)-4-HYDROXYTAMOXIFEN (C15-1257-602)
Price: $1,276.09List Price: $1,417.88Application (Z)-4-Hydroxytamoxifen has been used: as a media supplement to study the cell viability by WST-1 Assay for inducing deletion of transforming growth factor-β (TGF-β gene in mice to induce Cre recombinase activity in vitro .