STUDresearch · Non-peptide

GW0742

Also known as

GW-0742 · GW 0742 · GW610742 · GW-610742 · Fitorine · Lipoline (forum trade nicknames) · Super Cardarine (community nickname) · Advanced Cardio (vendor branding)

Community talk. May contain inaccuracies. Not medical advice. Not a protocol. Not for human or animal use.

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Non-peptide Niche talk Systemic Oral Metabolic research compounds

Systemic — a whole-body selective PPARδ/β agonist discussed as shifting muscle fuel use toward fatty-acid oxidation, not a local or injection-site agent.

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Timing context & sources

Half-life in the body

No numerical human plasma parent-compound half-life was established in the checked GW0742 source.

A controlled 15 mg oral administration study detected urinary metabolites for up to 20 days and parent compound briefly at low concentration, but its accessible abstract did not report plasma elimination half-life.

Abstract-only review; participant count and full sampling table were unavailable there. Urinary metabolite detection is not parent half-life, biological activity or a dosing interval.

Felt duration people report

Felt duration is disputed: one user later described effects for two to three days on an intermittent schedule, while other users reported no endurance effect at all.

The same detailed author first stopped 10 mg/day on day 3 because of adverse symptoms, later used 4 mg twice weekly and then added MK-677; separate commenters reported null experiences.

Anonymous reports, unverified products, changing schedules, home measurements and multi-compound confounding prevent a reliable duration range.

  • Reddit r/cardarine — GW0742 in-depth review (opens in a new tab)Original post and same-author updates: adverse stop on day 3 at 10 mg/day, later 4 mg Monday/Thursday with two-to-three-day subjective effects, then an MK-677-confounded update.One evolving uncontrolled account, unverified product, schedule changes, subjective measures, home scale estimates and later polypharmacy.
  • Reddit r/sarmssourcetalk — GW0742, your experiences (opens in a new tab)Comments include weight loss without endurance, no difference from Cardarine, and no endurance response despite claimed exposure up to 20 mg/day.Sparse anonymous accounts; unknown product authenticity, no objective training protocol or outcome assessment, and possible selection bias.
  • Reddit r/sarmssourcetalk — SR9011 and GW0742 (opens in a new tab)Original post described injected GW0742 plus SR9011 for about eight weeks and reported little cardiovascular advantage compared with Cardarine.Two-drug combination, unusual unverified route and products, retrospective comparison and no objective or blinded measures.

What people say 12

  • Endurance talk: Same primary search intent as Cardarine — longer sessions, easier steady-state cardio, less “gas tank empty” feel; public log volume is much smaller. forum
  • Vs Cardarine reports conflict: One detailed user reported only modest benefit at a later lower intermittent schedule and severe early adverse effects at 10 mg/day; other commenters reported no endurance advantage, including one claiming exposure up to 20 mg/day. Product identity remained uncertain. forum
  • Fat-loss adjacency: Forums market adipose breakdown / recomp help while preserving lean mass on a cut; diet, cardio volume, and co-drugs usually confound single-agent credit. forum
  • Non-androgenic appeal: No classic AAS androgen sides (acne/voice/hair from androgen receptor agonism) — draws cutters stacking SARMs who want cardio without more androgen load. forum
  • Bloodwork anecdotes: Scattered logs claim improved lipids, triglycerides, and fasting glucose on panels during use; sample size tiny and stacks/diet confounded. anecdote
  • “200× stronger” marketing: Some vendor/forum posts claim up to ~200× potency vs GW501516; published EC50s for both sit near ~1 nM on PPARδ, so structural similarity and near-identical potency argue against that slogan as a literal assay fact. forum
  • Lipids / cholesterol (mice): ~10 mg/kg GW0742 associated with reverse cholesterol transport and increased fecal excretion of HDL-derived cholesterol in mouse work; not a human lipid-drug claim. animal
  • Insulin resistance (rats): Intravenous GW0742 lowered plasma glucose/insulin and attenuated elevated HOMA-IR in fructose-rich-diet diabetic rats in a dose-related fashion; blocked by the PPARδ antagonist GSK0660. animal
  • Anti-inflammatory (rodents): Models report lower leukocyte recruitment and cytokines (e.g., IL-6, IL-1β, TNF-α) at research doses such as ~30 mg/kg in LPS pulmonary inflammation; also gut I/R and pancreatitis models. animal
  • Pulmonary / right-heart research: GW0742 studied for vessel relaxation and limiting right-heart hypertrophy in hypoxia/PAB-type models (often ~10–30 mg/kg ranges in papers) — research endpoints, not fitness protocols. animal
  • Neuro / microglial research: Seven-day GW0742 (fitorine) ~5 mg/kg/day i.p. used in rat temporal-lobe epilepsy / neuroinflammation gene-expression work. animal
  • Human athletic outcomes: Gray-market dosing charts rest on little controlled human performance data; most “results” are self-reports. trial

Doses people talk about 14

  • Core forum band: Most written protocols copy Cardarine culture at roughly 10–25 mg/day oral, once daily. forum
  • 10 mg/day report: One detailed user stopped after three days because of cardiovascular and systemic symptoms. This is an adverse self-report, not a conservative or safe-dose designation. forum
  • Lower “typical protocol” talk: Some depth posts/reviews float ~4–10 mg/day as a typical research/user band when marketing claims higher potency. forum
  • Advanced / high end of charts: ~20–25 mg/day appears as upper community discussion; some logs/coaches claim ~25 mg/day for max endurance push — still anecdote-driven. forum
  • “Do not exceed” vendor/forum lines: Multiple secondary write-ups say not to go past ~25 mg/day — rule-of-thumb marketing, not a trial MTD. forum
  • Sex-split vendor charts (unvalidated): Research-chemical sellers sometimes list ~10 mg/day (male subjects) and ~5 mg/day (female subjects) — not from large human trials. forum
  • Once-daily vs split: Claimed ~24 h half-life drives once-daily dosing for most; a minority split higher totals AM/PM or dose nearer pre-workout for perceived acute coverage. forum
  • Caps/tabs: 10 mg tablet products appear under various brand names; still research-chemical supply, not pharma. forum
  • With food: Some vendor blurbs say food may aid absorption; not a settled PK claim. forum
  • Allometric warning: Do not treat 10 mg/kg rodent doses as 10 mg/kg human doses; community “cancer HED” debates for the sibling compound already show how messy conversion arguments get. forum
  • Uncertainty / identity risk: Labeled milligrams may not be real GW0742 (underdose, different GW, solvent residue); third-party testing is rare compared with demand. forum
  • Framing: Community charts, vendor labels, and animal mg/kg only — not medical advice, not validated human protocols, not proof of identity/purity. forum
  • Route gap in papers: Fitness forums = oral liquids/caps; published work often uses oral gavage, IV (e.g., HOMA-IR rat work to reduce PK noise), or IP in DMSO vehicles. animal
  • Animal scale (not human recipes): Rodent/work ranges in the literature include sub-mg/kg boluses (e.g., 0.03–0.3 mg/kg in some acute injury models), ~0.3 mg/kg i.p. daily in bleomycin fibrosis work, ~5 mg/kg/day i.p. for multi-day CNS models, ~10 mg/kg for reverse cholesterol transport, and ~10–30 mg/kg oral/systemic in pulmonary-vascular and inflammation papers. animal

How it may feel 8

  • First days can diverge sharply: One 10 mg/day self-report stopped on day 3 after headache, nausea, thirst, fatigue, irritability, tachycardia and irregular beats; other users reported no endurance effect. forum
  • Later reports remain mixed: The same user later described two positive weeks on 4 mg twice weekly and then better runs after adding MK-677, while other users reported weight loss without endurance, no difference from Cardarine or no effect. forum
  • Weeks 3–4: Common keep/stop/switch checkpoint; some compare back-to-back with GW501516 or abandon for better-logged options. forum
  • Weeks 6–8: Typical end of Cardarine-borrowed blocks; endurance ease may be clearer if product is real and training is cardio-heavy. forum
  • Weeks 8–12: Vendor/forum upper cycle talk; still not GW0742-specific trial timelines. forum
  • Potency anecdotes at equal mg: Reports of needing extra carbs in hard sessions to avoid “going hypo” on ~10 mg/day exist alongside “felt nothing” logs — both are anecdotal. anecdote
  • No change by ~3–4 weeks: Threads question authenticity, under-dosing relative to chart, solvent degradation, or unrealistic expectations rather than endless escalation. forum
  • Day 0 framing: Not a caffeine-style stim; most expect quiet nuclear-receptor onset over days, not an instant buzz. forum

Cycles people discuss 10

  • Default culture block: ~8 weeks oral, borrowed wholesale from Cardarine forums. forum
  • Extended chart range: 8–12 weeks appears on secondary dosage pages and some vendor “research cycle” blurbs. forum
  • Conservative / probe lengths: 2–4 weeks to compare feel vs GW501516 or to test a new bottle; 4–6 weeks for lower-risk preference. forum
  • 8–10 week self-limits: Some experienced users cap phases around 8–10 weeks at ~10 mg explicitly because of class carcinogenicity debate. forum
  • Time off: Often match “on” length in risk threads (e.g., 8 on / 8 off); not standardized and not evidence-based for this molecule specifically. forum
  • No classic AAS PCT: PPARδ agonists are not framed as suppressing HPTA the way androgens do; PCT only enters when stacked with SARMs/AAS. forum
  • Blast/cruising adjacency: Anecdotes include running GW in final oral weeks of a blast and first 4–6 weeks post-blast as a “cleanup / cardio / lipids” adjunct — multi-agent context. anecdote
  • Continuous months: A minority report multi-month continuous Cardarine/“Super Cardarine” use; cancer-risk and heart-growth discussions make that controversial even among enthusiasts. forum
  • Re-runs: Fewer public multi-cycle GW0742 logs than Cardarine; many people try once and return to better-stocked GW501516. forum
  • Women’s talk: Same class goals at lower chart doses (~5 mg/day vendor talk); almost no dedicated long logs. forum

Timing 9

  • Why once daily: Long assumed coverage + Cardarine schedule copy; some still prefer pre-workout timing for “feel” even if receptor effects are genomic. forum
  • Downstream nature: Nuclear-receptor / gene-expression fuel shift — not a short-acting stimulant buzz; training effects are discussed over days–weeks. forum
  • Carnitine depletion talk (class/forum): Some stack discussions claim GW use depletes carnitine and pair L-carnitine — mechanistic folklore around fat oxidation, not a settled GW0742-specific trial endpoint. forum
  • Human half-life not established here: A controlled 15 mg oral excretion study found urinary metabolites for up to 20 days but did not report a plasma parent-compound half-life. Urine detectability cannot justify a once-daily schedule. trial
  • Anti-doping excretion study (human oral 15 mg single dose): Sobolevsky et al. (Drug Test Anal.): parent drug only briefly at low ng/mL; sulfone (bisoxygenated) metabolites are the practical urine targets. trial
  • Detection windows (same 15 mg oral comparison): GW1516-sulfone reported detectable up to ~40 days; GW0742-sulfone up to ~20 days; urinary abundance of GW0742 and metabolites ~10× lower than GW1516 at equal dose. trial
  • Sulfoxide:sulfone ratio: Reported to vary irregularly (~1:3 to 1:15) with time after dose — lab method detail, not a user timing tip. trial
  • Washout of “feel” vs detectability: Subjective endurance ease fading is not the same as metabolite clearance; athletes subject to testing face multi-week risk after a single oral exposure in the cited method. trial
  • Animal PK caveat: IV vs oral/IP differences matter when reading glucose/IR or inflammation papers — route changes exposure dramatically. animal

More on what it is 9

  • Why people search it: Same endurance + fat-oxidation goals as Cardarine, with marketing that it is “stronger/cleaner per mg”; still far quieter public logs than GW501516. forum
  • Mechanism talk: PPARδ activation upregulates fatty-acid oxidation / oxidative metabolism genes in muscle (CPT1, UCP3, PDK4, PGC-1α family talk) and can favor fat-as-fuel over pure glucose reliance during long work. forum
  • Caveat: Supply is thinner and mislabeling risk higher than Cardarine; many “dose charts” are pure GW501516 culture copy. forum
  • What it is: Small-molecule selective PPARδ/β agonist from GlaxoSmithKline; CAS 317318-84-6; also catalogued as GW610742 / fitorine; forum nicknames include Lipoline and “Super Cardarine.” trial
  • Chemistry snapshot: Thiazole-based PPAR ligand (C21H17F4NO3S2, ~471.5 g/mol) structurally close to Cardarine (GW501516) — often described as a patent/sibling tool compound rather than a wholly new class. trial
  • Potency on paper: Published cell assays commonly cite ~1 nM EC50 at human PPARδ with ~1000-fold selectivity over PPARα (~1.1 μM) and PPARγ (~2 μM) — same ballpark as GW501516, not a 200× EC50 gap. lab
  • Off-target notes: Literature also reports dose-dependent mixed PPARβ agonist/antagonist behavior, weak multi-nuclear-receptor activity including AR and VDR antagonism, and in-silico thyroid-receptor interaction talk — not pure single-target lore. lab
  • Evidence honesty: Mostly animal and cell work plus sparse gray-market anecdotes; no large human athletic RCTs establishing dose, efficacy, or long-term safety. animal
  • Not: Not a SARM, not a steroid/androgen, not FDA-approved for fat loss or endurance, and not a proven “safer Cardarine” just because it is less famous. trial

Stacks 12

  • Vs / sequential with Cardarine (GW501516): Most common comparison pair; some alternate trials, few rationalize stacking both PPARδ agonists together (redundant receptor class). forum
  • + SR9009 (Stenabolic): Classic endurance/fat-ox research-chem pairing; oral SR9009 bioavailability is itself heavily debated (injectable SR talk in some advanced threads). forum
  • + Ostarine (MK-2866): Cut/recomp SARM base + GW for cardio — multi-agent logs. forum
  • Vendor “Super Lean Stack” example: Marketed fixed blend of MK-2866 20 mg + SR9009 20 mg + GW0742 20 mg per capsule — illustrates ratio culture, not a studied protocol; pre-mixes prevent independent titration. forum
  • + Andarine (S4) / S23: Documented log example aiming fat loss while holding weight: S4 ~50 mg/day + S23 ~20 mg/day + GW0742 ~10 mg/day (± test base in that log). anecdote
  • + RAD-140: Endurance-coach style stacks in some forums pair GW family compounds with RAD and (sometimes injectable) SR9009 — highly confounded. forum
  • + Creatine (HCL or mono): Non-PED pairing frequently praised for training output alongside Cardarine/“Super Cardarine.” forum
  • + L-carnitine: Mentioned when carnitine-depletion lore is accepted; evidence quality low. forum
  • Contest prep / hard cut: High cardio + deficit + often multiple agents — rarely clean single-agent attribution. forum
  • Testosterone / AAS base: Used as a non-androgenic cardio/fat adjunct under a blast rather than as solo mass gear. forum
  • Not stacked for PCT: Does not replace SERM/AI logic when androgens are in the stack. forum
  • Basics still dominate outcomes: Sleep, calories, and conditioning volume get credit whenever results look good. forum

Storage notes 2

  • No mix instructions here: STUDresearch does not list reconstitution, diluent volumes, or syringe unit charts. People reconstitute many different ways and vial labels differ — that content creates more confusion than clarity. forum
  • Storage (general talk only): Unopened research products are usually kept cool, dry, and away from light per the seller label. Anything after first use is product-specific — follow the label, not a universal forum SOP. forum

Watch for 17

  • Not a free pass for 0742: Lack of an equally famous GW0742 cancer bioassay in public discussion is not proof of safety — shared mechanism is the point of the caution. forum
  • Sparse community acute sides: Occasional headache, GI upset, fatigue, oily-skin/acne talk borrowed from Cardarine threads — causality often unclear with polypharmacy. forum
  • Hypoglycemia-ish training anecdotes: Rare reports of needing extra carbs mid-session on potent-feeling ~10 mg days — still anecdote, not a labeled indication. anecdote
  • Anecdotal mass / imaging scares: Isolated Reddit-style reports of unexpected findings during/after GW use (e.g., renal masses later called benign) circulate as harm-reduction stories; not established causal epidemiology. anecdote
  • Source / identity risk: Mislabeling (including vs GW501516), wrong strength, solvent contamination, and underdosing are first-line practical risks. forum
  • Pregnancy / unknown populations: No responsible community protocol for pregnancy, adolescence, or uncontrolled illness — data vacuum. forum
  • Polypharmacy stacks: Adding S4/S23/RAD/test/orals multiplies sides and confounds attribution; GW does not cancel androgen toxicity. forum
  • Class cancer caution (sibling compound): GW501516 multi-organ tumors in long-term high-dose rodent bioassays (GSK abstracts; ~3 mg/kg/day class often cited; ~104-week designs) drove abandonment of clinical development and class-wide wariness for other strong PPARδ agonists including GW0742. animal
  • Human long-term gap: No robust multi-year gray-market safety database; short forum use cannot rule out rare or delayed harms. trial
  • Cardiac growth / calcineurin: Wagner et al. and related work link PPARβ/δ stimulation (including GW0742) to rapid cardiac growth and angiogenesis via calcineurin pathways in animal/cell systems — forums translate this into “cardiomegaly” fear language. animal
  • Context-dependent heart effects: Other models report GW0742 limiting pathological right-heart hypertrophy or improving contractility endpoints — direction depends on model, dose, and disease state; not a green light for unsupervised use. animal
  • Hepatic / muscle alterations: Faiola et al. found PPARα (more than PPARδ) mediated some hepatic and skeletal-muscle changes after GW0742 — reminder that “selective” is relative at high exposure. animal
  • Dose-dependent inflammation patterns: Animal literature shows anti-inflammatory benefits in some designs but bidirectional cytokine / response patterns by context and dose. animal
  • High in-vitro exposure toxicity: Cerebellar neuron and other cell models show neuroprotection at brief exposures but toxicity (e.g., LDH release, c-Jun) after prolonged high concentrations (~100 μM range in classic papers). lab
  • WADA / sport: PPARδ agonists sit in metabolic-modulator prohibited territory; validated methods detect GW0742 metabolites — sanction risk for tested athletes even after short oral exposure. trial
  • Not approved / research-only: Not an approved medicine for performance, fat loss, or metabolic disease in standard consumer channels; animal metabolic benefits do not equal human benefit–risk. trial
  • Australia / scheduling context for sibling: GW501516 has been treated as a high-risk prohibited substance in multiple jurisdictions — social/legal spillover affects how the whole GW family is discussed. trial

Updated: 2026-08-12

Evidence mix Mostly community / anecdote tags Full: every bullet (trial + community). Use Scan for a faster bro-science read.

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