SYS · ONLINEPASS · 63.0%
Open Assay
Independent Testing / Est. 2026
BATCH04·26·B
PASS63.0%
N27
PeptidesOtherKisspeptin-10

Kisspeptin-10

/ 10-amino-acid C-terminal fragment of kisspeptin; KISS1R (GPR54) receptor agonist
TIER 2 · TranslationalN = 0 · TESTING PENDINGLAST REVIEW 2026·04·20

ALIAS · KP-10 · Metastin 45-54

Pass rate
0
Samples
0
Suppliers
Research use onlyAny dose figures below describe what specific cited studies used, reported factually. Nothing on this page is guidance for human use.READ FIRST →

Terms in this page you can click for a plain-English popup: , , , , , , , .

§ A · Identity
Primary sequence— sequence not captured —
MW · CLASS · 10-amino-acid C-terminal fragment of kisspeptin; KISS1R (GPR54) receptor agonistCATEGORY · Other

Substantial academic research interest in reproductive endocrinology — kisspeptin triggers GnRH release. Several Phase 1/2 academic trials exist (e.g., UK Imperial College group). Not an FDA-approved therapeutic.

§ B · Mechanism of action

Kisspeptin-10 is the C-terminal 10 amino acids of the 54-amino-acid kisspeptin peptide encoded by KISS1. It is a potent agonist at KISS1R (formerly GPR54) and triggers GnRH release from hypothalamic GnRH neurons. Central to the hypothalamic control of the reproductive axis.

§ C · Human clinical evidence

Several Phase 1/2 academic trials have evaluated kisspeptin infusion for conditions including hypothalamic amenorrhea, infertility-adjacent indications, and diagnostic applications (triggering oocyte maturation in IVF). Imperial College London group is a major research center. Not FDA-approved for any therapeutic use.

§ F · Safety signal

Academic trials at research doses have reported generally favorable tolerability with mild flushing and short-lived infusion-related effects. Long-term safety data from chronic administration is not available.

§ H · Regulatory status

Regulatory status

FDA status:
Not FDA-approved
§ I · Notable gaps and controversies

Kisspeptin is a well-characterized research peptide with legitimate academic clinical investigation, but popular-press marketing claims (libido, body composition, etc.) outrun the specific reproductive-endocrinology indications under study.