CINDURA

Wild harvested

20 Times More Muscle Strength

A synergistic and patent protected combination of two natural ingredient

  • Natural Ingredients
  • Improves Muscle strength &
  • endurance
  • Proven Safety
  • Clinically Proven
  • Dose : 800 mg daily
  • Free flowing powder
  • Formulation friendly

Turns On mTOR Signaling To Stimulate Muscle Protein Synthesis In Skeletal Muscle Cells

Activates Endothelial Nitric Oxide Synthase (Enos) To Improve Blood Flow & Reduce Fatigue

Improves Serum Testosterone

Activates AMPK in Skeletal Muscle Cells

May Reduce Muscle Wasting Via Inhibition Of Ubiquitin

Tablets

Capsules

Ready to Drink Powders

Nutritional Bars

Cindura offers un parallel advantage as it can be formulated in Capsules, Tablets, Powder, Shots and many exciting forms of food and beverages.

Clinical Study

A double blinded placebo controlled clinical study in healthy trained subjects demonstrated efficacy and tolerability of CinDura®

Key Benefits

  • Significantly improves muscle strength and
    endurance
  • Improves cardio-pulmonary endurance
  • Promotes muscle growth
  • Improves lean body mass
  • Improves serum testosterone
  • May reduce muscle wasting as indicated
    through suppressed Ubiquitin Proteasome
    activity in vitro

Subject Disposition

Day-0 Screening; Day-7 Baseline; Day-21 (follow up after 2 weeks);

Day-35 (follow up after 4 weeks) and Day-49 (follow up after 6 weeks)

Improves Muscular Strength

Bar diagram represents mean change in muscle strength by 1-RM bench press in Placebo and CinDura® groups from baseline to Day 49. Each bar represents mean ± SD, *p<0.05 (ANCOVA) indicates change in muscular strength in treatment group was significant over placebo

Improves Muscular Strength

Bar diagram represents mean change in muscle strength by 1-RM leg press in Placebo and CinDura® groups
from baseline to Day 49. Each bar represents mean ± SD, *p<0.05 (ANCOVA) indicates change in muscular
strength in treatment group was significant over placebo

Improves Muscular Endurance

Bar diagram represents mean change in time to exhaust in Placebo and CinDura® groups from baseline to
Day 49. Exhaust time was measured as time of continuous treadmill exercise with increase in inclination every
5 minutes. The change in treadmill exhaust time of treatment group in comparison with the Placebo was
tested using ANCOVA;*p<0.05

Improves Time to Exhaust

Bar diagrams represent free testosterone level in circulation of resistance trained participants. Bars represent
mean±SD of free testosterone concentrations in the placebo and CinDura groups at baseline and at day 49. *
indicates significance (P<0.05 ) over baseline in un-paired t-test.

Improves Serum Testosterone

Bar diagrams represent mean change (cm) in left arm and right arm circumference respectively in Placebo
and CinDura® groups from baseline to Day 49. Each bar represents mean ± SD, *p<0.05 (ANCOVA) indicates
change in arm girth in treatment group was significant over placebo.

Improves Body Composition

Bar diagrams represent mean change (kg) in Lean body mass and fat mass respectively in Placebo and
CinDura® groups from baseline to Day 49. The bars represent mean changes (± SD) from baseline Lean Body
Mass and Total Body Fat at day 49. Comparison between the groups were analyzed using ANCOVA; *P<0.05

Safety Studies

CinDura® is safe for human consumption

CinDura® tested using a battery of toxicity studies as per OECD test guidelines

Toxicity Studies

  • Acute oral toxicity : LD50 > 2000 mg/kg B. Wt.
  • Acute dermal toxicity : LD50 > 2000 mg/kg B. Wt.
  • Acute dermal irritation study : Non-irritant to skin
  • Acute eye irritation study : Non-irritant to eye
  • 28 D Repeated Oral Tox study: NOAEL > 1000
    mg/Kg
  • 90 D Repeated Oral Tox study: NOAEL > 1500
    mg/Kg

Genotoxicity Studies

CinDura® is safe for human consumption

AMES test

Non mutagenic at highest concentration tested (5000 µg/mL)

In vivo Micronucleus assay

Non mutagenic at 2000 mg/kg

In vitro Chromosomal aberration test

Non mutagenic at 125 µg/mL

In vivo Studies

Efficacy Study in Albino Mice

Healthy Swiss albino mice were randomly divided into three groups
(n=5). Mice were treated with:

  • Vehicle (Group-1) or
  • CinDura® 150mg/kg (Group-2) or
  • Caffeine 10mg/kg (Group-3) for 21 days.
  • One hour after the treatment on day 21, all the mice were tested for
    the energy endurance using forced swimming test.
  • This test was monitored by using SMART video tracking system
    (Panlab S.L.U).
  • The total path length of swimming (distance travelled) and average
    velocity were measured

Efficacy Study 1 in Swiss Albino Mice

Supplementation of CinDura® increases Mean velocity
Distance travelled

The bar diagrams A and B represent Average Swimming Velocity and Total distance travelled respectively.
The bars 1 to 3 represents vehicle control, CinDura® (150 mg/kg ) and Caffeine (10 mg/kg) treated groups
respectively. Each bar represents Mean ± SEM, n=5.

Efficacy Study 2 in Swiss Albino Mice

Supplementation of CinDura® increases energy and
endurance

Supplementation of CinDura® improves muscle
strength

In vitro studies &
Mechanism of Action

Improves Nitric Oxide Production

Activates mTOR signaling

CinDura® activates cellular protein
synthesis machinery through
activation of mTOR signaling, helping
increased protein synthesis in skeletal
muscle cells

Upregulate Myogenic Factors

CinDura® improves skeletal muscle
development through
up-regulation of transcription factors
involved in myogenesis

Induce Myotube Formation

Phase contrast micrographs showing Myotube formation in C2C12 mouse myoblasts; Vehicle, 10 and 100 ng/ml Cindura® (A, B & C respectively) Immunofluorescence images showing Myosin Heavy Chain protein expression in Vehicle, 10 and 100 ng/ml Cindura® treated C2C12 cells (D, E & F respectively) Arrow heads indicate multinucleated myotubes

CinDura® induces myotube formation in myoblasts indicating support for
building skeletal muscle fibers

Improves Nitric Oxide Production

CinDura® might reduce muscle wasting via inhibiting the Ubiquitin
Proteasome Pathway as shown in L6 rat skeletal myoblasts

Protection from Oxidative stress
induced mitochondrial dysfunction

CinDura® helps recovering from H2O2 induced depolarized mitochondrial
membrane in L6 rat skeletal myoblasts, thus maintaining healthy mitochondrial
function under oxidative stress, e.g. during prolonged workout

Activates AMPK Signaling

CinDura® activates AMPK in skeletal
muscle cells, indicating increase in
glucose uptake, fatty acid oxidation,
and mitochondrial biogenesis

Reduces Proteasome Activity

CinDura® increases Testosterone production in MA10 mouse leydig cells

Increases Testosterone production

CinDura® might reduce muscle wasting via inhibiting the Ubiquitin
Proteasome Pathway

Free Radical Scavenging Activity

CinDura® exhibited dose dependent free radical scavenging activity by
increase in concentration