What is the catalog number for Teverelix?

The catalog number for Teverelix is HY-105173.

What sizes are available for Teverelix?

Teverelix is available in the following size(s): 1 Each.

Is Teverelix in stock?

Teverelix is currently made to order / not held in immediate stock. Contact us for lead time.

Who manufactures Teverelix?

Teverelix is manufactured by QuantiMol.

What is the estimated delivery time for Teverelix?

Estimated delivery time for Teverelix is approximately 15 business day(s), depending on your location.

Where can I find the safety data sheet (SDS/MSDS) for Teverelix?

The safety data sheet for Teverelix is available here: http://file.medchemexpress.com/batch_PDF/HY-105173/.

Teverelix

Teverelix (EP 24332) is a GnRH antagonist. Teverelix binds competitively and reversibly to GnRH receptors, thereby suppressing the release of LH and FSH. Teverelix can be used in the research of prostatic hyperplasia, endometriosis, and prostate cancer[1][2].

Product Specifications

CAS Number

151272-78-5

Product Name Alternative

EP 24332

UNSPSC

12352209

Target

GnRH Receptor; Histamine Receptor

Type

Peptides

Related Pathways

GPCR/G Protein; Immunology/Inflammation; Neuronal Signaling

Applications

Metabolism-protein/nucleotide metabolism

Field of Research

Cancer; Endocrinology

Assay Protocol

https://www.medchemexpress.com/teverelix.html

Solubility

10 mM in DMSO

Smiles

OC(C=C1)=CC=C1C[C@H](NC([C@H](CO)NC([C@@H](CC2=CN=CC=C2)NC([C@H](NC([C@H](NC(C)=O)CC3=CC4=CC=CC=C4C=C3)=O)CC5=CC=C(Cl)C=C5)=O)=O)=O)C(N[C@H](CCCCNC(N)=O)C(N[C@@H](CC(C)C)C(N[C@@H](CCCCNC(C)C)C(N6[C@@H](CCC6)C(N[C@H](C)C(N)=O)=O)=O)=O)=O)=O

Molecular Formula

C74H100ClN15O14

Molecular Weight

1459.13

References & Citations

[1]MacLean CM, et al. Pharmacokinetic, Safety, and Pharmacodynamic Properties of Teverelix Trifluoroacetate, a Novel Gonadotropin-Releasing Hormone Antagonist, in Healthy Adult Subjects. Clin Pharmacol Drug Dev. 2022 Feb;11 (2) :257-269. |[2]Sperduti S, et al. GnRH Antagonists Produce Differential Modulation of the Signaling Pathways Mediated by GnRH Receptors. Int J Mol Sci. 2019 Nov 7;20 (22) :5548.|[3]Deghenghi R, et al. Antarelix (EP 24332) a novel water soluble LHRH antagonist. Biomed Pharmacother. 1993;47 (2-3) :107-10. |[4]Fraser HM, et al. Initiation of high dose gonadotrophin-releasing hormone antagonist treatment during the late follicular phase in the macaque abolishes luteal function irrespective of effects upon the luteinizing hormone surge. Hum Reprod. 1997 Mar;12 (3) :430-5.