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Cat. No. Product Name Information
PC-60267

PHTPP

ERβ inhibitor

PHTPP is a potent, selective antagonist of estrogen ERβ receptor, exhibits 36-fold selective for ERβ.
PC-60063

Enclomiphene citrate

Enclomiphene citrate((E)-Clomifene, cis-Clomifene, RMI-16289, ICI-46476) is a nonsteroidal selective estrogen receptor modulator (SERM) that is under development for the treatment of male hypogonadism.
PC-45734

Elacestrant dihydrochloride

SERD

Elacestrant (RAD1901) dihydrochloride is a novel, orally bioavailable small-molecule selective estrogen receptor degrader (SERD).
PC-45733

Elacestrant

SERD

Elacestrant (RAD-1901) is a novel, orally bioavailable small-molecule selective estrogen receptor degrader (SERD).
PC-43271

AZD9496 maleate

A potent, selective estrogen receptor downregulator (SERD) with ER downregulation pIC50 of 9.68.
PC-43270

AZD9496

Estrogen receptor inhibitor

AZD9496 is a potent, selective estrogen receptor downregulator (SERD) with ER downregulation pIC50 of 9.68.
PC-42580

XCT790

ERRα inverse agonist

XCT790 (XCT-790) is a potent and selective ERRα inverse agonist with IC50 of 300-500 nM in transient transfection assays.
PC-46618

Clomiphene citrate

A non-steroidal, a widely used fertility agent that inhibits estrogen receptor in the hypothalamus.
PC-45541

Endoxifen hydrochloride

A metabolite of tamoxifen, orally active non-steroidal selective estrogen receptor modulator (SERM) for the treatment of estrogen receptor-positive breast cancer..
PC-45540

Endoxifen

SERM

Endoxifen is a metabolite of tamoxifen, orally active non-steroidal selective estrogen receptor modulator (SERM) for the treatment of estrogen receptor-positive breast cancer.
PC-45096

(Z)-4-Hydroxytamoxifen

A major metabolite of tamoxifen, a well-known Estrogen receptor antagonist in breast but partial estrogen receptor agonist in endometrium.
PC-45768

SNG-1153

ERα36 inhibitor

SNG-1153 (SNG1153) is a derivate of icaritin that inhibits the growth of lung CSCs, targets abnormal ERα36 activity, inhibits cell growth and induces apoptosis of BCR-ABL+ leukemic cells.

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