Miscellaneous & Research; Sleep, Mood & Stress
Galanin

Galanin is one of the body's own signalling peptides, and it is unusual in what it does: it mostly turns other signals down rather than up, everywhere from the brain to the gut to the pancreas. That inhibitory role is why it appears in work on feeding, pain, mood and stress resilience — including a recent finding, taken from inside a randomised placebo-controlled psilocybin trial in major depression, that psilocybin therapy lowered galanin in cerebrospinal fluid alongside noradrenaline. The human record here is that biomarker measurement plus a handful of small infusion studies. Galanin was first isolated in 1983, and there is no approved use for it anywhere.
Last updated
Mechanism
Acts at three G-protein-coupled receptors, GAL1 to GAL3, largely inhibiting neurotransmitter and hormone release.
Reported effects
What sources associate with this compound. Reported categories, not outcomes we have graded — each would need its own citation and rung.
- Feeding behaviour research
- Nociception research
- Neuroendocrine signalling context
Dosing on file unverified
IV bolus: 4 x 50 µg administered hourly; IV infusion: 80 pmol/kg/min for 60 min
Carried from a source that labels it unverified, and reproduced with that label attached. A record of what is reported, not a recommendation. No citation on this page establishes it.
Literature on file 6
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review or editorial
Galanin and Galanin Receptors (1999, cited 83x) graded on: indexed as "Review" - secondary literature, not a study — “Review”
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review or editorial
Expression of the Galanin system in the human pancreas, pancreatitis, and pancreatic cancer: Association with nodal involvement and perineural invasion. graded on: indexed as "Review" - secondary literature, not a study — “Review”
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review or editorial
Galanin receptor 2: A multifunctional modulator in neurological diseases - Structure, mechanisms, and therapeutic prospects. graded on: indexed as "Review" - secondary literature, not a study — “Review”
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review or editorial
Re-thinking neuropeptide therapeutics: What Neuropeptide Y and Galanin teach us about stress, resilience, and drug design. graded on: indexed as "Review" - secondary literature, not a study — “Review”
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human observational
CSF galanin and noradrenaline downregulation by psilocybin therapy in major depressive disorder. graded on: a secondary or post-hoc analysis — read from the indexed abstract — “secondary analysis”
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animal in vivo
Intracerebroventricular and intranasal application of alarin reduces body weight in male rats. graded on: an animal model — “rats”
Identity
Skeletal formulathe canonical depiction
Drawn by PubChem from CID 16133823, the identifier on this record.
- Molecular weight
- 3157.4
- Molecular formula
- C139H210N42O43
- CAS number
- 88813-36-9
- PubChem CID
- 16133823
- UniProt
- P22466 (precursor)
- InChI key
- CBSXZYWGVAQSHI-RUKUCZSXSA-N
- SMILES
- C[C@H]([C@@H](C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(=O)N)C(=O)N[C@@H](CO)C(=O)N[C@@H](C)C(=O)NCC(=O)N[C@@H](CC1=CC=C(C=C1)O)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(C)C)C(=O)NCC(=O)N2CCC[C@H]2C(=O)N[C@@H](CC3=CNC=N3)C(=O)N[C@@H](C)C(=O)N[C@@H](C(C)C)C(=O)NCC(=O)N[C@@H](CC(=O)N)C(=O)N[C@@H](CC4=CNC=N4)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@@H](CO)C(=O)N[C@@H](CC5=CC=CC=C5)C(=O)N[C@@H](CO)C(=O)N[C@@H](CC(=O)O)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CC(=O)N)C(=O)NCC(=O)N[C@@H](CC(C)C)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CO)C(=O)O)NC(=O)[C@H](CC6=CNC7=CC=CC=C76)NC(=O)CN)O
- InChI
- InChI=1S/C139H210N42O43/c1-65(2)38-84(165-121(206)86(40-67(5)6)166-123(208)88(43-75-31-33-79(188)34-32-75)161-106(193)55-151-114(199)70(11)157-131(216)97(59-182)175-127(212)95(49-104(144)191)170-122(207)87(41-68(7)8)173-136(221)112(72(13)186)180-130(215)90(159-105(192)51-141)44-76-52-150-81-27-19-18-26-80(76)81)116(201)154-58-109(196)181-37-23-30-101(181)134(219)172-91(45-77-53-147-63-155-77)120(205)158-71(12)115(200)178-111(69(9)10)135(220)153-57-108(195)162-94(48-103(143)190)126(211)168-92(46-78-54-148-64-156-78)125(210)164-83(29-22-36-149-139(145)146)119(204)174-98(60-183)132(217)167-89(42-74-24-16-15-17-25-74)124(209)176-99(61-184)133(218)171-96(50-110(197)198)128(213)163-82(28-20-21-35-140)118(203)169-93(47-102(142)189)117(202)152-56-107(194)160-85(39-66(3)4)129(214)179-113(73(14)187)137(222)177-100(62-185)138(223)224/h15-19,24-27,31-34,52-54,63-73,82-101,111-113,150,182-188H,20-23,28-30,35-51,55-62,140-141H2,1-14H3,(H2,142,189)(H2,143,190)(H2,144,191)(H,147,155)(H,148,156)(H,151,199)(H,152,202)(H,153,220)(H,154,201)(H,157,216)(H,158,205)(H,159,192)(H,160,194)(H,161,193)(H,162,195)(H,163,213)(H,164,210)(H,165,206)(H,166,208)(H,167,217)(H,168,211)(H,169,203)(H,170,207)(H,171,218)(H,172,219)(H,173,221)(H,174,204)(H,175,212)(H,176,209)(H,177,222)(H,178,200)(H,179,214)(H,180,215)(H,197,198)(H,223,224)(H4,145,146,149)/t70-,71-,72+,73+,82-,83-,84-,85-,86-,87-,88-,89-,90-,91-,92-,93-,94-,95-,96-,97-,98-,99-,100-,101-,111-,112-,113-/m0/s1
Also called
- Galanin (Research)
Notes unverified prose
Small human studies: Murck et al. 2004 (n≈12); Small human IV studies (Murck et al. 2004)
Not on file 2
1 of the 8 fields we track hold nothing on this record, and each says why. 1 further absence is named below. A blank field is a bug; a named absence is a finding.
- amino-acid sequencenothing we hold supplies it
- half-lifenothing we hold supplies it
Each field links to every other record missing the same thing. The full ledger holds 765 gaps across 163 records.
Listed prices 1
What 1 shop we track listed for Galanin, read from their own public catalogues on 2026-09-14. We take no commission on these and they are not ranked by any payment — how vendors are scored.
Compare prices1 listing from 1 shop
| Vendor | Size | Price | Per mg |
|---|---|---|---|
| VPeptide Canada | 10 mg | $100.00 CAD | $10.00/mg |
None of these shops lists your destination. Choose “Show all” to see every listing we hold.
Prices are the vendor's own listing, reproduced with the date we read it — never converted between currencies, and compared per milligram only where the vendor states the vial size.