Substance P
From PeptidePlaza, the free peptide reference · Entry #1038 · Nootropic · Sources fetched 2026-09-10 · Editorial standards
Substance P (also known as Neurokinin P, Neuropeptide sp-1, Sh-oligopeptide-73, Substance p (1-11)) is a nootropic research peptide. Substance P, also known as Neurokinin P, is an endogenous human peptide and a member of the tachykinin family.
Substance P is an endogenous human peptide belonging to the tachykinin family. It functions by exciting neurons, evoking behavioral responses, acting as a potent vasodilator and secretagogue, and contracting various smooth muscles. With over 24,000 papers, it is a well-studied compound, with research exploring its role as a "Friend or Foe" in clinical medicine and its broader pharmacological implications. It is currently in an investigational regulatory status.
1 Mechanism of action
Tachykinins are active peptides which excite neurons, evoke behavioral responses, are potent vasodilators and secretagogues, and contract (directly or indirectly) many smooth muscles
2 Chemical and physical properties
| CAS number | 33507-63-0 |
|---|---|
| Molar mass | 1347.6 g/mol |
| Purity (typical) | Not independently verified |
| Storage | −20 °C, lyophilised powder, desiccated |
| Solubility | Sterile water / bacteriostatic water |
2.1 Amino acid sequence
RPKPQQFFGLM
3 Research studies (8)
- Substance P-Friend or Foe
Journal of clinical medicine (2022) - Substance P
Pharmacological reviews (1983) · Review - Substance P
Lancet (London, England) (1976) - Substance P
European journal of pain (London, England) (2000) · Review - Substance P
British medical bulletin (1982) · Review - Substance P
Vitamins and hormones (1977) · Review - Substance P
Life sciences (1974) · Review - The Regenerative Potential of Substance P
International journal of molecular sciences (2022) · Review
4 Safety and risk profile
4.1 Regulatory status
Substance P is currently classified as Investigational. It has no approved human indication in the United States; availability elsewhere does not imply demonstrated safety or efficacy.
5 Frequently asked questions
- What is Substance P?
- Substance P, also known as Neurokinin P, is an endogenous human peptide. It is classified as a tachykinin, a family of active peptides that play various roles in the body.
- How does Substance P work?
- Substance P functions by exciting neurons and evoking behavioral responses. It is also a potent vasodilator, meaning it widens blood vessels, and a secretagogue, which stimulates secretion. Additionally, it can contract many smooth muscles, either directly or indirectly.
- What is the regulatory status of Substance P?
- Substance P is currently in an investigational regulatory status. This means it is still undergoing research and development and has not yet received approval for widespread clinical use.
- What is Substance P studied for?
- Substance P is extensively studied, with research exploring its multifaceted roles in the body, including its potential as both beneficial and detrimental in clinical medicine. Its pharmacological properties, such as its effects on neurons, blood vessels, and smooth muscles, are also key areas of investigation.
6 References
- Substance P — compound summary PubChem. View source
- Substance P — molecule record ChEMBL. View source
- Substance P — protein entry UniProt. View source
- Substance P — published literature (24,333 records) PubMed. View source
Related compounds
Entries that share a target, a mechanism, or a research area with Substance P.
Also nootropic
A low-molecular-weight peptide fraction from porcine brain tissue, used across Europe and Asia for stroke and dementia for decades. Decades of trials, and the Cochrane verdict is still not favourable.
Also nootropic
Vasoactive Intestinal Peptide (VIP) is a neuropeptide that activates VIP receptor 1 (VPR1) and VIP receptor 2 (VPR2), which are G protein-coupled receptors.
Also nootropic
A nine-amino-acid neuropeptide hormone best known for childbirth and lactation, now studied extensively for social bonding, stress regulation, wound healing, and metabolic effects via intranasal delivery.
Also nootropic
A cyclic heptapeptide melanocortin receptor agonist and active metabolite of Melanotan II. Unlike peripheral vasodilators, PT-141 acts centrally via the CNS to modulate arousal and food intake pathways.
Also nootropic
A potent cyclic analog of α-MSH that activates melanocortin receptors broadly. Studied for UV-independent melanogenesis, appetite suppression, and as the parent compound of PT-141 (Bremelanotide).
Also nootropic
Eptifibatide is an integrin alpha-IIb/beta-3 inhibitor used to decrease the rate of death or myocardial infarction in patients with acute coronary syndrome and those undergoing percutaneous coronary intervention.