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Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T9997 | GLL 398 | Estrogen Receptor/ERR | |
GLL 398 is an orally active and selective degrader of estrogen receptor with an IC50 of 1.14 nM. GLL 398 blocks tumor growth in xenograft breast cancer models. | |||
T5118 | Brilanestrant | GDC0810,GDC 0810,GDC-0810,ARN-810,RG 6046 | Estrogen Receptor/ERR , Estrogen/progestogen Receptor |
Brilanestrant (GDC-0810) is a selective estrogen receptor degrader (IC50: 0.7 nM). | |||
T39727 | ERα degrader-2 | ERK | |
ERα degrader-2 is a selective and potent estrogen receptor (SERD) degrader with anticancer activity, inhibits ERα, and has an EC50 value for estrogen receptor degradation of 0.3 nM.ERα degrader-2 can be used for the prev... | |||
T15788 | LSZ-102 | LSZ102 | Estrogen Receptor/ERR |
LSZ-102 is an effective and selective degrader of estrogen receptor (IC50 = 0.2 nM) and can be used in studies about ERα positive breast cancer. | |||
T13674 | Elacestrant | RAD1901 | Estrogen Receptor/ERR , Estrogen/progestogen Receptor |
Elacestrant (RAD1901) with IC50s of 48 and 870 nM for ERα and ERβ, respectively.Elacestrant is an orally available selective estrogen receptor degrader . | |||
T13675 | Elacestrant dihydrochloride | RAD1901 dihydrochloride | Estrogen/progestogen Receptor |
Elacestrant dihydrochloride (DA-DKRAD1901 dihydrochloride) is an orally available selective estrogen receptor degrader with IC50s of 48 for ERα and 870 nM for ERβ, respectively. | |||
T12832 | Amcenestrant | SAR439859 | Estrogen Receptor/ERR , Estrogen/progestogen Receptor |
Amcenestrant (SAR439859) is an orally active, nonsteroidal and selective degrader of estrogen receptor (SERD). SAR439859 is a potent antagonist of ER (with an EC50 of 0.2 nM for ERα degradation). | |||
T39499 | Rintodestrant | G1T48 | |
Rintodestrant (G1T48) is an orally active, non-steroidal, selective estrogen receptor degrader (SERD) that also functions as a CDK4/6 inhibitor. | |||
T39118 | AZD9496 maleate | ||
AZD9496 maleate is a highly potent and selective antagonist of the estrogen receptor alpha (ERα), exhibiting an IC50 value of 0.28 nM. This compound, AZD9496 maleate, is an orally bioavailable selective estrogen receptor... | |||
T39368 | GNE-149 | ||
GNE-149 is an orally bioavailable compound that acts as a full antagonist of estrogen receptor α (ERα) with an IC50 of 0.053 nM. It is also classified as a selective estrogen receptor degrader (SERD). GNE-149 holds poten... | |||
T70179 | THIQ-40 | ||
THIQ-40 is a novel potent erα antagonist and selective estrogen receptor degrader (serd), exhibiting good oral bioavailability, antitumor efficacy, and serd activity in vivo | |||
T63922 | ERα degrader 5 | ||
ERα degrader 5 is an orally active, selective estrogen receptor (ER) reducer that acts on ERα (EC50: 1.1 nM). ERα degrader 5 shows anti-tumour effects in vivo. | |||
T74856 | ER degrader 4 | ||
ER degrader 4, a selective and orally active compound, effectively degrades estrogen receptors and exhibits anti-tumor activity [1]. | |||
T11173 | Elacestrant S enantiomer | RAD1901 S enantiomer | Others |
Elacestrant S enantiomer is a selective and orally available estrogen receptor (ERR) degrader with IC50 values of 48 and 870 nM for ERα and ERβ, respectively. | |||
T79382 | ER degrader 6 | Estrogen Receptor/ERR | |
ER degrader 6 (compound 35s) is a potent selective estrogen receptor modulator (SERM) with the capacity to degrade Estrogen Receptor (ER)α. It disrupts the microtubule network, inhibiting tubulin polymerization, and effe... | |||
T63674 | Imlunestrant | ||
Imlunestrant is a selective, orally active estrogen receptor degrader (SERD) that can be used in ER+ and HER2 breast cancer studies. | |||
T74593 | Taragarestrant meglumine | ||
Taragarestrant (D-0502) meglumine is a potent, orally active, and selective estrogen receptor degrader (SERD) demonstrating significant efficacy in ER+ breast cancer cell lines and xenograft models [1] [2]. | |||
T11173L | Elacestrant S enantiomer dihydrochloride | RAD1901 S enantiomer dihydrochloride,RAD-1901 S enantiomer dihydrochloride,RAD 1901 S enantiomer dihydrochloride | Others |
Elacestrant (RAD1901) dihydrochloride is a selective and orally available estrogen receptor (ERR) degrader with IC50 values of 48 and 870 nM for ERα and ERβ, respectively. Elacestrant S enantiomer dihydrochloride is an l... | |||
T74415 | Imlunestrant tosylate | ||
Imlunestrant tosylate (LY-3484356) is a potent, orally active selective estrogen receptor degrader (SERD) exhibiting purely antagonistic properties. It effectively maintains inhibition of estrogen receptor (ER)-dependent... | |||
T63165 | LX-039 | ||
LX-039 is a potent, selective, orally active estrogen receptor degrader (EC50: 2.99 nM) with antitumor effects.LX-039 has indole C-3 chloride atoms.LX-039 has good pharmacokinetic properties in mice, low clearance, high ... |