This information is for research and educational purposes only. No medical recommendations. Products are not approved for human use. For health questions, consult a doctor.

Lexicon

Lipo-C 120mg

Lipotropic amino acid-vitamin blend supporting hepatic fat metabolism in research settings.

2 min read 11 sources

Lipo-C glass vial with red solution and the black TPD label on a white podium, next to blue 3D molecule models in a bright lab
No study of its own · not approved

Summary

At a glance

Sources checked on 26 Oct 2026

On the blend itself
0 trials

no trial of methionine, inositol and choline as a blend on ClinicalTrials.gov, as of 26 Oct 202610

Men with organ damage without choline
77 %

fatty liver or muscle damage on a low-choline diet, 26 men in the study1

Until liver fat came back
10 weeks

after choline was stopped in the infusion, 15 patients fed through a vein2

Homocysteine with vitamin B12
-7 %

on top of folic acid, analysis of 12 trials with 1,114 people7

Waist with inositol
-2.36 cm

meta-analysis of 18 trials, low to very low certainty of evidence6

  • Lipo-C combines methionine, inositol, choline and vitamin B12. All four are nutrients the body needs for fat and methyl metabolism in the liver.43
  • ClinicalTrials.gov lists no trial of this blend. The numbers here come from studies on single components.10
  • Choline has the best evidence: without choline in the diet 77 percent of men and 80 percent of postmenopausal women developed a fatty liver or muscle damage.1
  • In patients fed through a vein, choline in the infusion improved liver values. Ten weeks after it was stopped the fat came back.2
  • In trials vitamin B12 lowered homocysteine by a further 7 percent on top of folic acid, inositol slightly reduced waist size. No study shows fat loss from the blend.76
Profile

Updated June 2026

Class
Amino acid-vitamin blend
Use
Hepatic metabolism

methylation pool

Half-life
Component-dependent

B12: ~6 days

Status
Research substance
Sizes
120mg/ml

1 size in the shop

Contents 12 sections
  1. At a glance
  2. What is Lipo-C?
  3. How it works
  4. Application and dosing
  5. What the research shows
  6. Research status
  7. Side effects
  8. Storage
  9. Related compounds
  10. FAQ
  11. Glossary
  12. Sources

What is Lipo-C?

Lipo-C is a defined blend of lipotropic substances combining methionine, inositol, choline and cyanocobalamin (B12). The compound supports liver fat metabolism through multiple parallel mechanisms.

The components are established and well-characterized: methionine and choline are central methyl donors, inositol is important for phospholipid structures, while B12 acts as a cofactor in methylation reactions. Research suggests the combination supports hepatic lipid metabolism, VLDL secretion and phosphatidylcholine synthesis.

Unlike peptide compounds, Lipo-C is not defined through a single receptor pathway but through parallel provision of multiple metabolic substrates. This makes it a complementary tool for metabolism research.

This information is for research and educational purposes only. No medical advice.

Comparison

What is in which blend

Components according to the TPD lexicon. MIC stands for methionine, inositol and choline. Tap a card to open its entry.

Simplified: the amounts per component differ. More components do not automatically mean more effect.

How it works

Lipo-C supports hepatic fat metabolism through the methylation axis and phospholipid metabolism:

  • Methyl-donor system: Methionine and choline provide methyl groups for SAM synthesis (S-adenosyl-methionine), essential for phospholipid synthesis and fat mobilization.
  • Phospholipid structure: Inositol and choline are components of membrane phospholipids, central to lipoprotein secretion.
  • Cofactor supply: B12 supports methylation pool regeneration and the homocysteine pathway.
  • VLDL pathway: The components together regulate the synthesis and secretion of VLDL particles from the liver.

Where it acts

Where the components act

Tap a point or a card. Colour = component. All from studies on single components, not on the blend.

  1. Liver

    Without choline in the diet many developed a fatty liver, choline in the infusion reduced the fat1

    MIC
  2. Muscle

    Choline deficiency caused muscle damage in some people1

    MIC
  3. Blood

    Vitamin B12 lowered homocysteine in the blood by a further 7 percent7

    B12
  4. Waist

    Inositol slightly reduced waist size in a meta-analysis6

    MIC

Targets in the ChEMBL database11

Three recorded mechanisms, type of action on each card.

Methionine adenosyltransferase 1A
Gene
MAT1A
UniProt
Q00266
ChEMBL
CHEMBL5169142
Action
Enzyme, turns methionine into SAM, the main methyl group donor
Choline kinase alpha
Gene
CHKA
UniProt
P35790
ChEMBL
CHEMBL3117
Action
Enzyme, first step from choline to phosphatidylcholine
Methionine synthase
Gene
MTR
UniProt
Q99707
ChEMBL
CHEMBL2150844
Action
Enzyme, needs vitamin B12 and turns homocysteine back into methionine
Glass cell made of honeycomb chambers, blue molecule models stream in from the left, golden droplets flow out through a channel on the right
Choline and methionine help the liver release fat as VLDL. Symbolic image.

Application and dosing

Dosing

Dosing, titration and syringe

Loading the dosing information …

  • Getting started and stepping up, drawn as a staircase
  • Units on the U-100 syringe for every step
  • How long one vial lasts
Glass vial with red solution, a blue cap and a black TPD label for Lipo-C, a disposable syringe beside it
Ready-made solution, subcutaneous or intramuscular. Symbolic image.

What the research shows

Preclinical studies document the role of Lipo-C components in lipid metabolism:

  • Methylation axis: The methionine-choline axis centrally regulates phospholipid turnover and VLDL secretion. Deficiencies are associated with fatty liver.
  • Phospholipid synthesis: Inositol as a component of phosphatidylinositol supports membrane signaling and lipoprotein structure.
  • One-carbon metabolism: B12 and methionine together regulate the one-carbon pool, central to DNA synthesis and cell proliferation.
  • Practical evidence: The combination has proven effective in American diet clinic tradition for decades, though robust clinical RCTs are rare.

Study results

What the trials measured

Interactive: switch tabs, tap points, show or hide arms. Arms are named relative to each other, no dosing advice.

Organ damage without choline1

Share with fatty liver or muscle damage on a low-choline diet, in percent

Men1 26 people
Low-choline diet 77%
Postmenopausal women1 15 people
Low-choline diet 80%
Premenopausal women1 16 people
Low-choline diet 44%

Controlled diet for up to 42 days. Those who developed organ damage got choline back, after which the values returned to normal. The study shows the need for choline, not the effect of an injection.

Liver density on CT2

Rise in Hounsfield units (HU), higher means less fat in the liver

Liver after 4 weeks2 Infusion with or without choline
Infusion without choline +5.8 HU
Infusion with choline +13.3 HU
Liver to spleen difference2 Comparison value in the same scan
Infusion without choline +1.3 HU
Infusion with choline +10.6 HU

15 patients fed almost entirely through a vein, 24 weeks. Liver values in the blood fell with choline, 10 weeks after it ended the fat came back. Choline was given in the infusion here, not as an injection under the skin.

A glass liver and a cluster of yellow fat cells in a glass display case on a white base
Studies exist on single components, not on the blend. Symbolic image.

Research status

Where the research stands

There is no registered trial of the blend. Studies on single components are shown above under the results. As of 26 Oct 2026. 10

  1. Preclinical No study of the blend, components known from nutrition research
  2. Phase 1 no registered trial
  3. Phase 2 no registered trial
  4. Phase 3 no registered trial
  5. Approval not yet
Not approved and no registered trial of the blend. Methionine, inositol, choline and vitamin B12 are nutrients.10

So far there is no registered trial in humans. 10

Side effects

Lipo-C is considered predominantly mild per research reports, as the components are individually well-characterized metabolic substrates.

  • Injection site: Redness, pressure, mild burning or transient irritation are the most common observations.
  • B12 component: Occasionally a sensation of warmth or mild tingling is reported shortly after application, typical for B12-containing blends.
  • Digestion: With higher-dosed blends, occasionally mild gastrointestinal discomfort is described.
  • Data limitations: Direct comparative studies on Lipo-C as a specific formulation are lacking. Long-term data are limited.

Storage

Lipo-C is an oil-based injection concentrate and should be stored at room temperature, protected from light. A refrigerator is not necessary and may destabilize the formulation.

Storage:

  • Room temperature (18-25°C)
  • Protected from light (dark bottle)
  • Store dry
  • Use within 60 days after opening

Related

Related compounds

Same components or a different path: all in the TPD lexicon.

FAQ

Common questions about Lipo-C 120mg

Short answers, each backed by the sources below.

Are there studies on Lipo-C itself?

No. As of 26 October 2026 the registry ClinicalTrials.gov lists no trial of methionine, inositol and choline as a blend. Everything shown here comes from studies on single components.10

Why is choline so important for the liver?

Choline has officially been an essential nutrient since 1998. In a controlled study with 57 adults on a low-choline diet 77 percent of men and 80 percent of postmenopausal women developed a fatty liver or muscle damage, before menopause it was 44 percent. With choline the values returned to normal.91

What does the study with choline in the infusion show?

15 patients fed almost entirely through a vein got their infusion with or without choline for 24 weeks. With choline liver density on CT rose much more after 4 weeks. That points to less fat. Liver values in the blood also fell. 10 weeks after it ended the fat came back.2

What role do methionine and vitamin B12 play?

The body makes SAM, the main donor of methyl groups, from methionine. Vitamin B12 helps the enzyme methionine synthase turn homocysteine back into methionine. In an analysis of 12 trials B12 lowered homocysteine by a further 7 percent on top of folic acid. As early as the 1930s choline prevented fatty liver in dogs, a lack of methyl groups caused it in rats and mice.487

What is known about inositol?

Myo-inositol acts similarly to insulin and lowers blood sugar after meals. A meta-analysis of 18 trials with 898 people found a BMI 0.57 points lower and a waist 2.36 cm smaller, with low certainty of evidence. The trials studied inositol as a supplement.56

Does Lipo-C help with weight loss?

That is not proven. There is no study of the blend. The well-studied effects of the components show mainly in a deficiency, such as fatty liver without choline.101

Which side effects are known?

There are no study data on the tolerability of the blend. The entry mainly names redness or burning at the injection site, occasionally a feeling of warmth from B12 and mild stomach complaints.10

Glossary

Terms explained briefly

Dotted words in the text open these explanations directly.

Fatty liver
Too much fat in the liver cells. Choline deficiency is a known cause.
Homocysteine
An intermediate of the methionine cycle. With vitamin B12 and folate it is turned back into methionine.
Lipotropic
Substances that help the liver process and export fat. They include choline, methionine and inositol.
Meta-analysis
A combined analysis of several studies on the same question. It is only as good as the studies it includes.
Methyl group donor
A substance that passes small carbon units (methyl groups) to other molecules, for example when building cell membranes.
MIC
Short for methionine, inositol and choline, the three classic lipotropic components.
Parenteral nutrition
Nutrition through an infusion into a vein when the gut cannot absorb enough food.
Phosphatidylcholine
A building block of cell membranes and lipoproteins. The liver needs it to export fat in packaged form.
SAM
S-adenosylmethionine: made from methionine and the cell's main methyl group donor.
VLDL
Fat transport particles the liver uses to release fat into the blood. Without choline the fat builds up in the liver.

Evidence

Sources

Show all 11 sourcesHide sources 9 Studies1 Trial registry1 Database checked 26 Oct 2026

Studies

  1. Choline requirement by sex and menopausal status, controlled diet

    Fischer et al., American Journal of Clinical Nutrition, 2007

    Checked 26 Oct 2026 via doi.org, Crossref, PubMed
  2. Choline in the infusion during parenteral nutrition, placebo-controlled

    Buchman et al., Journal of Parenteral and Enteral Nutrition, 2001

    Checked 26 Oct 2026 via doi.org, Crossref, PubMed
  3. Choline metabolism and fatty liver (review)

    Corbin und Zeisel, Current Opinion in Gastroenterology, 2012

    Checked 26 Oct 2026 via doi.org, Crossref, PubMed
  4. Methionine metabolism and liver disease (review)

    Mato et al., Annual Review of Nutrition, 2008

    Checked 26 Oct 2026 via doi.org, Crossref, PubMed
  5. Myo-inositol in metabolic diseases (review)

    Croze und Soulage, Biochimie, 2013

    Checked 26 Oct 2026 via doi.org, Crossref, PubMed
  6. Inositol and metabolic markers, meta-analysis of 18 trials

    Delavar et al., Diabetology & Metabolic Syndrome, 2025

    Checked 26 Oct 2026 via doi.org, Crossref, PubMed
  7. Lowering homocysteine with folic acid and B vitamins, meta-analysis

    Homocysteine Lowering Trialists' Collaboration, BMJ, 1998

    Checked 26 Oct 2026 via doi.org, Crossref, PubMed (ohne DOI, über Titel, Journal und Jahr)
  8. Vitamin B12, folate and the methionine cycle (review)

    Froese et al., Journal of Inherited Metabolic Disease, 2019

    Checked 26 Oct 2026 via doi.org, Crossref, PubMed
  9. Choline as an essential nutrient (review)

    Zeisel und da Costa, Nutrition Reviews, 2009

    Checked 26 Oct 2026 via doi.org, Crossref, PubMed

Trial registry

  1. Search on ClinicalTrials.gov (no trial with the blend)

    ClinicalTrials.gov, U.S. National Library of Medicine

    Checked 26 Oct 2026 via ClinicalTrials.gov API v2

Database

  1. Enzymes MAT1A, CHKA and MTR in UniProt

    UniProt (Q00266, P35790, Q99707), Target-IDs aus ChEMBL

    Checked 26 Oct 2026 via UniProt REST, ChEMBL API

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