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Novera supplies sexual health and hormonal peptide compounds to qualified researchers, laboratories, and scientific institutions. All materials in this category are sourced from USA GMP-certified manufacturers, verified by Certificate of Analysis (COA) for identity and purity, and catalogued exclusively for use in controlled experimental settings. This page provides molecular profiles, research classification data, and procurement information for compounds studied in hypothalamic-pituitary-gonadal (HPG) axis signaling assays, melanocortin receptor binding models, gonadotropin secretion marker profiling, and steroidogenesis pathway research in reproductive and endocrine cell line systems.
Gonadorelin 5mg – Synthetic GnRH Decapeptide for Preclinical HPG Axis Pharmacology, GnRH Receptor Binding Kinetics, and Hypothalamic-Pituitary Signaling Pathway Research A structurally defined synthetic gonadotropin-releasing hormone decapeptide studied for GnRH...
Research-grade synthetic GnRH analog peptide formulated in 10mg quantity for gonadotropin-releasing hormone studies and decapeptide research in controlled laboratory environments.
HCG 5000iu – LH Receptor Agonist Glycoprotein for Preclinical Gonadotropin Receptor Interaction and Signal Transduction Research A pharmaceutical-grade glycoprotein LH analog studied for Leydig cell LH receptor binding kinetics, downstream...
High-purity research compound supplied for controlled laboratory studies. HCG 12000 IU is distinguished by its high-activity standardized unit format, allowing precise quantitative comparison across endocrine-focused laboratory models. The defined 12000...
Kisspeptin 5mg from Novera is a hypothalamic neuropeptide functioning as a primary upstream regulator of the reproductive hormone cascade in experimental models. By stimulating GnRH neuron activation, Kisspeptin enables mechanistic...
Research-grade decapeptide signaling molecule formulated for experimental peptide pathway research in controlled laboratory environments.
Research-grade peptide intended for controlled laboratory studies. Oxytocin (5mg) is produced using advanced peptide synthesis methods designed for high structural accuracy and batch consistency. Each vial is prepared with strict...
Research-grade synthetic nonapeptide hormone formulated in 10mg quantity for peptide hormone structure studies and nonapeptide characterization research in controlled laboratory environments.
Research-grade synthetic peptide engineered for precision receptor-binding studies and advanced peptide-receptor interaction research in controlled laboratory settings.
This category is organized into two subcategories addressing distinct research domains within reproductive endocrinology and hormonal signaling investigation:
PT-141 (Bremelanotide) — 10 mg
| Sequence | Cyclic heptapeptide melanocortin analog: cyclo(Nle-Asp-His-D-Phe-Arg-Trp-Lys) |
| Molecular Weight | 1,025.18 Da |
| Format | Lyophilized powder, 10 mg vial |
| Purity | ≥98% (HPLC verified, COA on file) |
| Research Classification | Cyclic melanocortin receptor agonist; studied in MC3R and MC4R binding assays, cAMP pathway activation profiling in hypothalamic neuronal cell models, dopamine-melanocortin signaling crosstalk research, and neuroendocrine pathway cascade investigation relevant to sexual behavior receptor systems |
Kisspeptin-10 — 1 mg
| Sequence | 10-residue RF-amide neuropeptide: Tyr-Asn-Trp-Asn-Ser-Phe-Gly-Leu-Arg-Tyr-NH2 |
| Molecular Weight | 1,302.46 Da |
| Format | Lyophilized powder, 1 mg vial |
| Purity | ≥98% (HPLC verified, COA on file) |
| Research Classification | Hypothalamic RF-amide neuropeptide; studied in KISS1R/GPR54 receptor binding assays, GnRH pulse regulation models, downstream LH and FSH secretion marker profiling, and HPG axis signaling cascade research in hypothalamic and pituitary cell line systems |
GnRH (Gonadorelin) — 2 mg
| Sequence | Decapeptide: pGlu-His-Trp-Ser-Tyr-Gly-Leu-Arg-Pro-Gly-NH2 |
| Molecular Weight | 1,182.31 Da |
| Format | Lyophilized powder, 2 mg vial |
| Purity | ≥98% (HPLC verified, COA on file) |
| Research Classification | Native gonadotropin-releasing hormone decapeptide; studied in GnRH receptor (GnRHR) binding assays, pituitary gonadotroph cell line LH/FSH secretion profiling, IP3-PKC and cAMP signaling cascade research, and HPG axis regulatory dynamics in endocrine cell systems |
hCG Beta Subunit Peptide — 1 mg
| Sequence | Synthetic fragment corresponding to hCG beta-subunit determinant loop region; sequence varies by lot — consult COA |
| Molecular Weight | ~1,800–2,200 Da (fragment-dependent) |
| Format | Lyophilized powder, 1 mg vial |
| Purity | ≥95% (HPLC verified, COA on file) |
| Research Classification | hCG beta-subunit derived peptide fragment; studied in LH receptor (LHCGR) binding competition assays, steroidogenesis activation marker research in Leydig and granulosa cell line models, and gonadotropin receptor interaction investigation in reproductive endocrinology research |
PT-141 (Bremelanotide) is the primary melanocortin receptor research tool in this category. As a cyclic melanocortin analog derived from the MT-II sequence, it has been studied in published research for its selective binding affinity at MC3R and MC4R receptor subtypes expressed in hypothalamic neuronal cell models. Published assays have characterized its cAMP accumulation response in HEK293 cells transiently transfected with MC3R or MC4R constructs, its interaction with the dopaminergic system through D1 receptor co-expression models, and its downstream effects on oxytocin pathway gene expression in paraventricular nucleus-derived cell systems. These studies are conducted in vitro and do not constitute claims regarding sexual arousal or performance outcomes in subjects.
The regulation of GnRH pulsatility through upstream kisspeptin signaling is a well-characterized research axis in reproductive neuroendocrinology. Kisspeptin-10 has been studied in published research for its KISS1R/GPR54 receptor binding dynamics, Gq-PLC-IP3 calcium signaling cascade activation, and downstream GnRH secretion marker profiling in GT1-7 hypothalamic neuron cell line models. GnRH itself serves as the downstream experimental ligand in pituitary gonadotroph cell assays using LβT2 and αT3-1 cell lines, with published studies characterizing GnRH receptor (GnRHR) internalization dynamics, ERK1/2 and c-Fos pathway activation, and LH beta-subunit mRNA expression profiling under defined pulse frequency and amplitude conditions.
LH receptor (LHCGR) interaction research using gonadotropin peptide fragments represents an established domain in reproductive endocrinology cell biology. Published studies using MA-10 Leydig cell and KGN granulosa cell line systems have characterized LH receptor binding competition dynamics, StAR protein expression as a steroidogenesis initiation marker, cAMP-PKA cascade activation profiling, and CYP11A1 and CYP17A1 enzyme activity assays as downstream steroidogenesis markers. hCG beta-subunit peptide fragments are used in competitive binding assays and receptor interaction models to characterize the determinant loop region contribution to LH receptor engagement under controlled in vitro conditions.
Pituitary gonadotroph cell line models — principally LβT2 and the alpha gonadotrope precursor line αT3-1 — represent the primary in vitro system for studying GnRH-stimulated LH and FSH secretion dynamics. Published assays in this domain use perifusion systems to study LH secretion pulse parameters under varying GnRH frequency and amplitude inputs, static incubation ELISA-based LH/FSH quantification, and transcriptomic profiling of LHb, FSHb, and CGA subunit gene expression in response to defined GnRH receptor activation patterns. These in vitro cell biology assays characterize gonadotropin secretion pathway dynamics at the molecular level without reference to fertility or reproductive outcomes in organisms.
Researchers designing studies in reproductive neuroendocrinology, gonadotropin signaling, or steroidogenesis pathway investigation typically evaluate compound selection based on receptor subtype specificity — particularly MC3R versus MC4R selectivity for melanocortin analogs and KISS1R versus GnRHR binding for HPG axis tools — the upstream versus downstream position of each compound within the HPG axis regulatory hierarchy, molecular stability in endocrine cell culture media including serum-containing formulations, and COA-verified purity with peptidase stability data where assay media contains serum-derived enzymes.
Novera provides complete product specifications for each compound including molecular weight, sequence, storage conditions, and available presentation formats. Researchers are encouraged to review compound data sheets and cross-reference with primary reproductive endocrinology literature before finalizing protocols. Novera does not provide experimental design guidance, dosing parameters, or outcome interpretation.
Institutional procurement offices and principal investigators with multi-compound or volume supply requirements are invited to contact Novera’s research supply team to confirm batch availability, lot consistency documentation, and GMP certification status for each referenced material.
All compounds in this category are procured from USA-based GMP-certified manufacturing facilities. Standard quality documentation and protocols include:
Novera does not supply compounds for human or veterinary administration. All purchase documentation classifies materials as research and laboratory use only. Institutional and bulk procurement arrangements are available subject to qualification review.
In reproductive endocrinology and neuroendocrine research literature, sexual health and hormonal peptides refer to amino acid sequences studied for their interactions with signaling pathways governing HPG axis regulation, gonadotropin secretion dynamics, steroidogenesis cascade activation, and melanocortin receptor-mediated neuroendocrine signaling. These compounds encompass synthetic receptor agonists and analogs such as PT-141, studied at MC3R/MC4R in hypothalamic models; RF-amide neuropeptides such as Kisspeptin-10, studied as KISS1R ligands and upstream GnRH pulse regulators; endogenous releasing hormones such as GnRH, studied in pituitary gonadotroph cell assays; and gonadotropin subunit fragments studied in LH receptor binding competition models.
Classification within this category is based on documented molecular interaction profiles in published reproductive biology and endocrinology literature. No compound is represented as a libido enhancer, sexual performance agent, hormone therapy, or fertility treatment of any kind. All materials are supplied as experimental research tools for mechanistic investigation in qualified laboratory settings by trained scientific personnel operating under appropriate institutional and ethical oversight frameworks.
HEK293 cells stably or transiently transfected with human MC3R or MC4R constructs are the most widely used systems in published PT-141 receptor binding and functional assay research. These heterologous expression systems allow selective characterization of individual receptor subtype responses in isolation from endogenous melanocortin receptor co-expression. cAMP accumulation assays using HTRF- or ELISA-based cAMP quantification kits provide the primary functional readout for receptor activation. Researchers requiring endogenous receptor context should consult published data on MC4R expression levels in hypothalamic neuronal lines (GT1-7) and select assay conditions accordingly. Binding competition assays using radiolabeled NDP-alpha-MSH as a reference ligand provide Ki determination under defined receptor density conditions.
Kisspeptin-10, comprising the C-terminal decapeptide of the full Kisspeptin-54 (metastin) sequence, retains the RF-amide C-terminal motif responsible for KISS1R binding affinity and receptor activation. Published receptor pharmacology studies have demonstrated equivalent EC50 values for Kisspeptin-10 and Kisspeptin-54 in KISS1R calcium mobilization assays, with Kisspeptin-10 preferred in many laboratory settings due to its shorter sequence, greater synthetic accessibility, and more predictable stability profile in peptidase-containing assay media. Researchers designing KISS1R desensitization or receptor internalization studies should consult published kinetics data for both forms before selecting the appropriate tool compound for their specific assay endpoint.
For GnRH receptor (GnRHR) activation assays in pituitary cell line systems, appropriate controls include: native GnRH (this compound) as the positive receptor activation control; a GnRHR antagonist such as Cetrorelix or Antide at defined concentrations to confirm receptor-mediated response attribution; a scrambled GnRH sequence as a sequence specificity control; and vehicle-matched (sterile water or PBS) negative controls at matched volume. For assays examining GnRH pulse frequency effects on LH/FSH secretion in perifusion systems, a continuous infusion condition is used as the baseline comparator against pulsatile delivery conditions. Full GnRH receptor pharmacology reference data is available in published studies using the LβT2 cell line model.
Cyclic peptides such as PT-141 typically exhibit greater conformational rigidity and hydrophobicity compared to linear analogs of equivalent length, which affects reconstitution behavior. PT-141 is generally soluble in sterile water or PBS at research-use concentrations; however, in cases of incomplete dissolution, addition of a small volume of glacial acetic acid (0.1% v/v final) or DMSO (up to 5% v/v, validated for cytotoxicity in target cell line) can improve solubility. Researchers should verify cyclization integrity from the mass spectrometry data on the COA before use, as linear impurities from incomplete cyclization would exhibit different receptor binding profiles. Storage as lyophilized powder at -20°C with reconstituted aliquots used promptly is standard practice.
This website contains information on research compounds intended for laboratory use only. You must be 21 years or older to enter and view this content. By entering, you also agree that all products are for research use only and are not intended for human consumption.