Peptide
SS-20
Also known as
SBT-20 · SBT-020 · SBT20 · SBT 20 · Phe-D-Arg-Phe-Lys-NH2 · H-Phe-D-Arg-Phe-Lys-NH2 · Szeto-Schiller peptide SS-20 · Szeto-Schiller peptide 20 · SS20 · SS 20
Community talk. May contain inaccuracies. Not medical advice. Not a protocol. Not for human or animal use.
What it is
| Identity | SS-20, or SBT-20/SBT-020, is a synthetic four-amino-acid peptide studied for mitochondrial function. It is related to SS-31 but has different chemistry; MOTS-c and humanin are another group. |
|---|---|
| What mitochondrial function means here | Mitochondria produce energy inside cells. Steadier energy, recovery and longevity are reasons people discuss SS-20, but the record does not establish a dependable healthy-user response pattern. |
Notes
SS-20 is a synthetic peptide, also called SBT-20 or SBT-020, studied for mitochondrial function. People discuss energy, longevity and SS-31 comparisons, but direct SS-20 experience remains sparse.
A synthetic mitochondrial peptide. Its four-amino-acid sequence is Phe-D-Arg-Phe-Lys-NH2. Mitochondria produce energy inside cells. van Diemen et al. — Safety, pharmacokinetics and pharmacodynamics of SBT-020 in early Huntington’s disease (Official context · Accessed 2026-09-30)
Related to SS-31, with different chemistry. SS-20 lacks SS-31’s dimethyltyrosine, an amino acid responsible for direct radical scavenging. Animal work nevertheless finds cardiolipin binding: interaction with a membrane fat that helps organize energy production. That distinction explains why it can help some stressed mitochondria without behaving like SS-31 in every experiment. Birk et al. — Disruption of cytochrome c heme coordination during ischemia (Animal context · Accessed 2026-09-30)
Different from mitochondrial-derived peptides. MOTS-c and humanin belong to another peptide group. Their shared mitochondrial topic does not make them forms of SS-20.
Energy and longevity are the hoped-for benefits. Community descriptions connect healthier mitochondria with steadier energy, recovery and aging. The original discussion record treats SS-20 as a lesser-known sibling, not a stimulant or a compound with a dependable healthy-user response pattern. Those goals are reasons for interest, not established outcomes.
Forum enthusiasm is mainly about the SS family. Science for ME members share mitochondrial literature; the SS-20 passages describe an analog without direct scavenging, not a fatigue recovery diary. LongeCity members ask how SS peptides compare with MitoQ while quoting experiments where SS-20 failed to protect an isolated heart. Those are laboratory comparisons, not users reporting treatment success or failure. Science for ME — Treatment of mitochondria with antioxidants SS-19 and SS-31 (Community discussion · Accessed 2026-09-30) · LongeCity — Mitochondria-targeted peptide SS-31 (Community discussion · Accessed 2026-09-30)
Source context — van Diemen et al. — Safety, pharmacokinetics and pharmacodynamics of SBT-020 in early Huntington’s disease: Small, short, monitored disease-population trial, not wellness experience. Healthy-volunteer dose list is background, not separately inspected trial data. Discussion labels an additional multi-dose PK range Part 2 Day 7 although Part 2 sampling is described as trough-only; no correction or combined range inferred. The dose rationale also gives 0.76 mg/kg and 4.5 mg for 60 kg, which do not reconcile arithmetically; the intended correction is unknown. Main PMC browser URL was CAPTCHA-blocked, alternate public Europe PMC XML succeeded.
Source context — Birk et al. — Disruption of cytochrome c heme coordination during ischemia: Animal/isolated mitochondria and membrane assays; no personal energy, consumer dose, tissue half-life or duration inferred. Authors/Cornell disclose financial interests in licensed SS peptides.
Source context — Science for ME — Treatment of mitochondria with antioxidants SS-19 and SS-31: Patient-community literature discussion, not firsthand administration. Quoted review results stay laboratory-origin claims. Embedded tweet was not inspected on X and is not used as an SS-20 report.
Source context — LongeCity — Mitochondria-targeted peptide SS-31: SS-31-focused thread with research quotations and opinions. No SS-20 dose diary or measured personal response. Cell-safety speculation is not accepted as human safety. First open timed out; a second open returned the actual body.
What people notice
| Interest rather than a clear felt pattern | Steadier energy, recovery and longevity are hoped-for benefits. The records contain mainly SS-family literature discussion, without a dependable firsthand SS-20 response pattern. |
|---|---|
| Human-study context | A published SBT-020 study found no overall benefit on mitochondrial, motor or cognitive measures. Its exploratory subgroup findings are not healthy-user energy reports. |
Notes
Energy and longevity are the hoped-for benefits. Community descriptions connect healthier mitochondria with steadier energy, recovery and aging. The original discussion record treats SS-20 as a lesser-known sibling, not a stimulant or a compound with a dependable healthy-user response pattern. Those goals are reasons for interest, not established outcomes.
Forum enthusiasm is mainly about the SS family. Science for ME members share mitochondrial literature; the SS-20 passages describe an analog without direct scavenging, not a fatigue recovery diary. LongeCity members ask how SS peptides compare with MitoQ while quoting experiments where SS-20 failed to protect an isolated heart. Those are laboratory comparisons, not users reporting treatment success or failure. Science for ME — Treatment of mitochondria with antioxidants SS-19 and SS-31 (Community discussion · Accessed 2026-09-30) · LongeCity — Mitochondria-targeted peptide SS-31 (Community discussion · Accessed 2026-09-30)
No overall benefit on the study’s function measures. Mitochondrial, motor and cognitive outcomes showed no overall benefit versus placebo. Subgroup signals remained exploratory. van Diemen et al. — Safety, pharmacokinetics and pharmacodynamics of SBT-020 in early Huntington’s disease (Official context · Accessed 2026-09-30)
Investigational amounts, separately from community claims. Active early-Huntington’s study arms used 5, 15 or 25 mg SubQ daily for seven days; after ≥1 month’s washout, 25 mg daily for 28 days. Earlier healthy-volunteer assessments used 5, 10, 20 and 30 mg. van Diemen et al. — Safety, pharmacokinetics and pharmacodynamics of SBT-020 in early Huntington’s disease (Official context · Accessed 2026-09-30)
Source context — Science for ME — Treatment of mitochondria with antioxidants SS-19 and SS-31: Patient-community literature discussion, not firsthand administration. Quoted review results stay laboratory-origin claims. Embedded tweet was not inspected on X and is not used as an SS-20 report.
Source context — LongeCity — Mitochondria-targeted peptide SS-31: SS-31-focused thread with research quotations and opinions. No SS-20 dose diary or measured personal response. Cell-safety speculation is not accepted as human safety. First open timed out; a second open returned the actual body.
Source context — van Diemen et al. — Safety, pharmacokinetics and pharmacodynamics of SBT-020 in early Huntington’s disease: Small, short, monitored disease-population trial, not wellness experience. Healthy-volunteer dose list is background, not separately inspected trial data. Discussion labels an additional multi-dose PK range Part 2 Day 7 although Part 2 sampling is described as trough-only; no correction or combined range inferred. The dose rationale also gives 0.76 mg/kg and 4.5 mg for 60 kg, which do not reconcile arithmetically; the intended correction is unknown. Main PMC browser URL was CAPTCHA-blocked, alternate public Europe PMC XML succeeded.
Doses people talk about
| Online chart claim | One reference lists 1–5 mg subcutaneously daily without a matching dosing study or personal log. It is not an established SS-20 community band. |
|---|---|
| Borrowed amounts | Older 2–5, 5–10 and 10–20+ mg injectable bands were borrowed without a dependable SS-20 course. A separate promotional 5–10 mg daily row actually names SS-31. |
| Human research amounts | Early-Huntington's study arms used 5, 15 or 25 mg subcutaneously daily for seven days, then 25 mg daily for twenty-eight days after at least a month washout. These are investigational exposures, separate from community claims. |
Notes
1–5 mg per administration is a chart claim. PeptideWiki lists daily subcutaneous use, meaning under the skin. It supplies no matching dosing study or personal log. This is an online reference claim, not an established SS-20 community band. PeptideWiki — SS-20 calculator and reference (Community guide · Accessed 2026-09-30)
SS-31 amounts do not transfer to SS-20. The original record preserves borrowed injectable bands of 2–5 mg, 5–10 mg and 10–20+ mg, without a dependable SS-20 course behind them. A promotional Reddit chart actually labels its 5–10 mg daily SubQ row SS-31. Neither provides SS-20-specific dosing evidence. JustBacWater — The Only Peptide Cheat Sheet You'll Need (Community guide · Accessed 2026-09-30)
Investigational amounts, separately from community claims. Active early-Huntington’s study arms used 5, 15 or 25 mg SubQ daily for seven days; after ≥1 month’s washout, 25 mg daily for 28 days. Earlier healthy-volunteer assessments used 5, 10, 20 and 30 mg. van Diemen et al. — Safety, pharmacokinetics and pharmacodynamics of SBT-020 in early Huntington’s disease (Official context · Accessed 2026-09-30)
Source context — PeptideWiki — SS-20 calculator and reference: Creator/reference chart, not personal experience. No named study supports 1–5 mg per administration or two-hour half-life. The page incorrectly excludes published human SBT-020 research. Arithmetic modeling and calculator recipes are not retained.
Source context — JustBacWater — The Only Peptide Cheat Sheet You'll Need: Commercial influence is explicit through vendor links and discount code. This row is SS-31, not SS-20; included solely to identify borrowed numbers, not to supply an SS-20 protocol. Publicly available post/replies, not all collapsed replies.
Source context — van Diemen et al. — Safety, pharmacokinetics and pharmacodynamics of SBT-020 in early Huntington’s disease: Small, short, monitored disease-population trial, not wellness experience. Healthy-volunteer dose list is background, not separately inspected trial data. Discussion labels an additional multi-dose PK range Part 2 Day 7 although Part 2 sampling is described as trough-only; no correction or combined range inferred. The dose rationale also gives 0.76 mg/kg and 4.5 mg for 60 kg, which do not reconcile arithmetically; the intended correction is unknown. Main PMC browser URL was CAPTCHA-blocked, alternate public Europe PMC XML succeeded.
Half-life, onset & duration
| Felt onset | No reproducible SS-20 benefit onset in these records. Expectations of energy changes in weeks two to four were borrowed from SS-31 discussion, not SS-20 diaries. |
|---|---|
| Felt duration | No identifiable account follows an SS-20 systemic benefit through a dose, a day and a break. Daily schedules do not establish how long a benefit feels noticeable. |
| Half-life | Day-seven human study values were 3.13, 3.94 and 4.14 hours in the 5, 15 and 25 mg arms. The online two-hour estimate is an assumption, not that measurement or a felt-effect window. |
| Blood peak | The human study reports plasma peaks at 0.5–1 hour. That is separate from benefit onset, which these accounts do not establish. |
Notes
No reproducible SS-20 benefit onset was found. The original notes describe SS-31 expectations of steadier energy in weeks two to four being borrowed for SS-20. They are not SS-20 diaries. The opened forums also discuss literature rather than a firsthand course, so there is no sound hours-to-days promise here. Science for ME — Treatment of mitochondria with antioxidants SS-19 and SS-31 (Community discussion · Accessed 2026-09-30) · LongeCity — Mitochondria-targeted peptide SS-31 (Community discussion · Accessed 2026-09-30)
Felt duration and benefit after stopping are unknown. There is no identifiable SS-20 account here that follows a systemic benefit through a dose, a day and a break. Older notes also flag scarce months-long experience. Neither a daily schedule nor a mitochondrial mechanism establishes how long someone would feel better.
Investigational amounts, separately from community claims. Active early-Huntington’s study arms used 5, 15 or 25 mg SubQ daily for seven days; after ≥1 month’s washout, 25 mg daily for 28 days. Earlier healthy-volunteer assessments used 5, 10, 20 and 30 mg. van Diemen et al. — Safety, pharmacokinetics and pharmacodynamics of SBT-020 in early Huntington’s disease (Official context · Accessed 2026-09-30)
Measured plasma timing, not a felt-effect clock. Day-seven half-lives were 3.13, 3.94 and 4.14 hours, respectively. Other reported summaries: 3.47–3.74 hours single-dose; 3.51–5.26 hours multiple-dose, inconsistently phase-labeled. These are not averaged. Blood peaks: 0.5–1 hour. Weekly sampling found no accumulation across 28 days. van Diemen et al. — Safety, pharmacokinetics and pharmacodynamics of SBT-020 in early Huntington’s disease (Official context · Accessed 2026-09-30)
Two hours is an assumption in an online reference. PeptideWiki attributes its value to similarity with related peptides, not human SS-20 measurements. Plasma half-life describes falling blood concentration; it cannot time a benefit or justify repeat dosing. PeptideWiki — SS-20 calculator and reference (Community guide · Accessed 2026-09-30)
Source context — Science for ME — Treatment of mitochondria with antioxidants SS-19 and SS-31: Patient-community literature discussion, not firsthand administration. Quoted review results stay laboratory-origin claims. Embedded tweet was not inspected on X and is not used as an SS-20 report.
Source context — LongeCity — Mitochondria-targeted peptide SS-31: SS-31-focused thread with research quotations and opinions. No SS-20 dose diary or measured personal response. Cell-safety speculation is not accepted as human safety. First open timed out; a second open returned the actual body.
Source context — van Diemen et al. — Safety, pharmacokinetics and pharmacodynamics of SBT-020 in early Huntington’s disease: Small, short, monitored disease-population trial, not wellness experience. Healthy-volunteer dose list is background, not separately inspected trial data. Discussion labels an additional multi-dose PK range Part 2 Day 7 although Part 2 sampling is described as trough-only; no correction or combined range inferred. The dose rationale also gives 0.76 mg/kg and 4.5 mg for 60 kg, which do not reconcile arithmetically; the intended correction is unknown. Main PMC browser URL was CAPTCHA-blocked, alternate public Europe PMC XML succeeded.
Source context — PeptideWiki — SS-20 calculator and reference: Creator/reference chart, not personal experience. No named study supports 1–5 mg per administration or two-hour half-life. The page incorrectly excludes published human SBT-020 research. Arithmetic modeling and calculator recipes are not retained.
Cycles people discuss
| No SS-20 calendar established | Four-to-eight-week evaluations and three-months-on/one-off language were borrowed from SS-31. Cost, needles and local irritation explain pauses in the old discussion, without validating an SS-20 cycle. |
|---|
Notes
No SS-20 on/off consensus is established. The original record includes borrowed four-to-eight-week evaluation windows and three-months-on, one-month-off language, explicitly traced to SS-31 comparisons. The Reddit guide’s four-to-eight-week course and two-to-four-week break likewise belong to SS-31. Cost, daily needles and local irritation are preserved reasons people discuss pausing, not a validated SS-20 calendar. JustBacWater — The Only Peptide Cheat Sheet You'll Need (Community guide · Accessed 2026-09-30)
Source context — JustBacWater — The Only Peptide Cheat Sheet You'll Need: Commercial influence is explicit through vendor links and discount code. This row is SS-31, not SS-20; included solely to identify borrowed numbers, not to supply an SS-20 protocol. Publicly available post/replies, not all collapsed replies.
Stacks
| No specific combination established | The saved record mainly lists mitochondrial neighbors such as MOTS-c, humanin, NAD precursors, CoQ10 and PQQ. SS-31 comparisons or sequencing stories are not documented SS-20 combination outcomes. |
|---|
Notes
Stack talk is adjacency rather than demonstrated synergy. The preserved discussion places SS-20 alongside MOTS-c, humanin, NAD precursors, CoQ10, PQQ, urolithin A and methylene blue. The familiar SS-31-before-MOTS-c story is not evidence for SS-20 sequencing. Sleep and training changes complicate subjective comparisons; silence is not a reason to assume the dose was too low.
Vs SS-31 (primary comparison, not a stack): Discussed as the non-Dmt sibling / historical control peptide. Dual SS-20 + SS-31 stacks are low-volume and poorly documented; most serious talk is which analog, not both. [community]
Watch for
| Local reactions | The human study recorded mild redness, swelling, pain and itching, generally starting within minutes and resolving within an hour. This does not establish consumer-product safety. |
|---|---|
| Identity and safety gaps | SS-31 substitution, uncertain contents, long-term healthy-user safety, pregnancy and medicine interactions remain concerns. Theoretical cancer discussion is not a demonstrated SS-20 cancer effect. |
Notes
Local reactions occurred in the human study. Redness, swelling, pain and itching were mild, generally starting within minutes and resolving within an hour. Consumer-product safety remains unknown. van Diemen et al. — Safety, pharmacokinetics and pharmacodynamics of SBT-020 in early Huntington’s disease (Official context · Accessed 2026-09-30)
Identity and missing safety information matter. Community cautions include substitution with SS-31, uncertain contents and little long-term healthy-user information. Older mitochondrial discussions raise theoretical cancer concerns; these are not demonstrated SS-20 cancer effects. Pregnancy, medication interactions and complex mitochondrial illness cannot be resolved through generic peptide charts.
Source context — van Diemen et al. — Safety, pharmacokinetics and pharmacodynamics of SBT-020 in early Huntington’s disease: Small, short, monitored disease-population trial, not wellness experience. Healthy-volunteer dose list is background, not separately inspected trial data. Discussion labels an additional multi-dose PK range Part 2 Day 7 although Part 2 sampling is described as trough-only; no correction or combined range inferred. The dose rationale also gives 0.76 mg/kg and 4.5 mg for 60 kg, which do not reconcile arithmetically; the intended correction is unknown. Main PMC browser URL was CAPTCHA-blocked, alternate public Europe PMC XML succeeded.
Full notes
SS-20 is a synthetic peptide, also called SBT-20 or SBT-020, studied for mitochondrial function. People discuss energy, longevity and SS-31 comparisons, but direct SS-20 experience remains sparse.
What SS-20 actually is
- A synthetic mitochondrial peptide. Its four-amino-acid sequence is Phe-D-Arg-Phe-Lys-NH2. Mitochondria produce energy inside cells. Official context
- Related to SS-31, with different chemistry. SS-20 lacks SS-31’s dimethyltyrosine, an amino acid responsible for direct radical scavenging. Animal work nevertheless finds cardiolipin binding: interaction with a membrane fat that helps organize energy production. That distinction explains why it can help some stressed mitochondria without behaving like SS-31 in every experiment. Animal context
- Different from mitochondrial-derived peptides. MOTS-c and humanin belong to another peptide group. Their shared mitochondrial topic does not make them forms of SS-20. Community
Why people are interested
- Energy and longevity are the hoped-for benefits. Community descriptions connect healthier mitochondria with steadier energy, recovery and aging. The original discussion record treats SS-20 as a lesser-known sibling, not a stimulant or a compound with a dependable healthy-user response pattern. Those goals are reasons for interest, not established outcomes. Community
- Protection in injured organs remains preclinical context. Rat kidney experiments support mitochondrial protection during interrupted blood flow; separate mouse kidney and cell experiments report less oxidative stress and inflammation. Neither establishes improved everyday energy or treatment of kidney disease in people. Animal context Animal context
Doses people encounter online
- 1–5 mg per administration is a chart claim. PeptideWiki lists daily subcutaneous use, meaning under the skin. It supplies no matching dosing study or personal log. This is an online reference claim, not an established SS-20 community band. Community guide
- SS-31 amounts do not transfer to SS-20. The original record preserves borrowed injectable bands of 2–5 mg, 5–10 mg and 10–20+ mg, without a dependable SS-20 course behind them. A promotional Reddit chart actually labels its 5–10 mg daily SubQ row SS-31. Neither provides SS-20-specific dosing evidence. Community Community guide
Half-life claims
- Two hours is an assumption in an online reference. PeptideWiki attributes its value to similarity with related peptides, not human SS-20 measurements. Plasma half-life describes falling blood concentration; it cannot time a benefit or justify repeat dosing. Community guide
When it might be felt
- No reproducible SS-20 benefit onset was found. The original notes describe SS-31 expectations of steadier energy in weeks two to four being borrowed for SS-20. They are not SS-20 diaries. The opened forums also discuss literature rather than a firsthand course, so there is no sound hours-to-days promise here. Community Science for ME forum LongeCity · AgingResearch
How long an effect lasts
- Felt duration and benefit after stopping are unknown. There is no identifiable SS-20 account here that follows a systemic benefit through a dose, a day and a break. Older notes also flag scarce months-long experience. Neither a daily schedule nor a mitochondrial mechanism establishes how long someone would feel better. Community
Cycles and time off
- No SS-20 on/off consensus is established. The original record includes borrowed four-to-eight-week evaluation windows and three-months-on, one-month-off language, explicitly traced to SS-31 comparisons. The Reddit guide’s four-to-eight-week course and two-to-four-week break likewise belong to SS-31. Cost, daily needles and local irritation are preserved reasons people discuss pausing, not a validated SS-20 calendar. Community Community guide
What to watch for
- Local reactions occurred in the human study. Redness, swelling, pain and itching were mild, generally starting within minutes and resolving within an hour. Consumer-product safety remains unknown. Official context
- Identity and missing safety information matter. Community cautions include substitution with SS-31, uncertain contents and little long-term healthy-user information. Older mitochondrial discussions raise theoretical cancer concerns; these are not demonstrated SS-20 cancer effects. Pregnancy, medication interactions and complex mitochondrial illness cannot be resolved through generic peptide charts. Community
Community comparisons and expectations
- Forum enthusiasm is mainly about the SS family. Science for ME members share mitochondrial literature; the SS-20 passages describe an analog without direct scavenging, not a fatigue recovery diary. LongeCity members ask how SS peptides compare with MitoQ while quoting experiments where SS-20 failed to protect an isolated heart. Those are laboratory comparisons, not users reporting treatment success or failure. Science for ME forum LongeCity · AgingResearch
- A guide misses the human trial. Longevity Archive says no human research exists. SBT-020’s published study contradicts that claim; its results are described below. The Longevity Archive · coach-written guide Official context
- Stack talk is adjacency rather than demonstrated synergy. The preserved discussion places SS-20 alongside MOTS-c, humanin, NAD precursors, CoQ10, PQQ, urolithin A and methylene blue. The familiar SS-31-before-MOTS-c story is not evidence for SS-20 sequencing. Sleep and training changes complicate subjective comparisons; silence is not a reason to assume the dose was too low. Community Community
What the human study measured
- Investigational amounts, separately from community claims. Active early-Huntington’s study arms used 5, 15 or 25 mg SubQ daily for seven days; after ≥1 month’s washout, 25 mg daily for 28 days. Earlier healthy-volunteer assessments used 5, 10, 20 and 30 mg. Official context
- Measured plasma timing, not a felt-effect clock. Day-seven half-lives were 3.13, 3.94 and 4.14 hours, respectively. Other reported summaries: 3.47–3.74 hours single-dose; 3.51–5.26 hours multiple-dose, inconsistently phase-labeled. These are not averaged. Blood peaks: 0.5–1 hour. Weekly sampling found no accumulation across 28 days. Official context
- No overall benefit on the study’s function measures. Mitochondrial, motor and cognitive outcomes showed no overall benefit versus placebo. Subgroup signals remained exploratory. Official context
