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Chemical Structure| 332382-54-4 Chemical Structure| 332382-54-4

Structure of ML-SA1
CAS No.: 332382-54-4

Chemical Structure| 332382-54-4

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ML-SA1 is an activator of TRPML1-3. It induces TRPML-mediated Ca2+ release from lysosomes.

Synonyms: Mucolipin synthetic agonist 1

4.5 *For Research Use Only !

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Product Details of ML-SA1

CAS No. :332382-54-4
Formula : C22H22N2O3
M.W : 362.42
SMILES Code : O=C1N(CC(N2C(C)(C)CC(C)C3=C2C=CC=C3)=O)C(C4=C1C=CC=C4)=O
Synonyms :
Mucolipin synthetic agonist 1
MDL No. :MFCD01956583
InChI Key :KDDHBJICVBONAX-UHFFFAOYSA-N
Pubchem ID :2880983

Safety of ML-SA1

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H301-H410
Precautionary Statements:P273-P301+P310-P501
Class:6.1
UN#:2811
Packing Group:

Isoform Comparison

Biological Activity

In Vitro:

Cell Line
Concentration Treated Time Description References
HEK293T cells 10 μM ML-SA1 induced significant [Ca2+]cyt increases Nat Commun. 2012 Mar 13;3:731
human fibroblasts 25 μM ML-SA1 activated whole-endolysosome currents Nat Commun. 2012 Mar 13;3:731
CHO cells 20 μM ML-SA1 induced rapid increases in GCaMP3 fluorescence Nat Commun. 2012 Mar 13;3:731
HEK293T cells 10 μM To validate the activation of TRPML1 channels by ML-SA1, results showed that ML-SA1 significantly increased current density. Nat Commun. 2018 Oct 10;9(1):4192
DT40 cells 25 μM In ITPR TKO DT40 cells, ML-SA1 response was significantly enhanced, indicating TMBIM6 regulates lysosomal calcium release independently of ITPR Autophagy. 2021 Mar;17(3):761-778
HT1080 cells 25 μM Measure ML-SA1-induced lysosomal calcium release, showing increased calcium release in TMBIM6-overexpressing cells Autophagy. 2021 Mar;17(3):761-778
neurons 100 μM 22 minutes To investigate the selective modulation of retrograde transport of LEs/amphisomes by TRPML1-mediated Ca2+ efflux. Results showed that ML-SA1 treatment significantly decreased the percentage of retrograde LT+ LAMP1 vesicles, increased the proportion of nonmotile vesicles, and increased pause time and frequency. Sci Adv. 2022 Apr 29;8(17):eabj5716
FIG4 knockout fibroblasts 40 µM 36 hours ML-SA1 dramatically reduced the proportion of cells with enlarged LAMP1 positive organelles in FIG4 knockout fibroblasts. Acta Neuropathol Commun. 2020 Oct 15;8(1):165
LITAF knockout fibroblasts 40 µM 36 hours ML-SA1 reduced the proportion of cells with enlarged LAMP1 compartments in LITAF knockout fibroblasts. Acta Neuropathol Commun. 2020 Oct 15;8(1):165
Fibroblasts from CMT1C patients (L125P and T115N mutations) 40 µM 36 hours ML-SA1 was able to rescue the vacuolation phenotype of LITAF knockout, FIG4 knockout and CMT1C patient fibroblasts. Acta Neuropathol Commun. 2020 Oct 15;8(1):165
mouse podocytes 20 μM ML-SA1 significantly reduced exosome concentration in the culture medium of podocytes and enhanced lysosome-multivesicular body (MVB) interaction. Redox Biol. 2021 Jul;43:102013
Primary rat oligodendrocyte precursor cells 20 μM 72 hours ML-SA1, as a TRPML1 channel agonist, partially rescues darunavir- and saquinavir-induced inhibition of oligodendrocyte differentiation J Neuroimmune Pharmacol. 2021 Mar;16(1):169-180

In Vivo:

Species
Animal Model
Administration Dosage Frequency Description References
Male BALB/c mice Single or multiple uranium exposure models Intraperitoneal injection 400 or 800 μg/kg Single administration, evaluated after 24 hours To evaluate the therapeutic effect of ML-SA1 on uranium-induced nephrotoxicity, results showed that ML-SA1 significantly reduced uranium accumulation in the kidney, mitigated renal proximal tubular injury, and increased apical exocytosis of lysosomes. Nat Commun. 2023 Jul 6;14(1):3997

Protocol

Bio Calculators
Preparing Stock Solutions 1mg 5mg 10mg

1 mM

5 mM

10 mM

2.76mL

0.55mL

0.28mL

13.80mL

2.76mL

1.38mL

27.59mL

5.52mL

2.76mL

References

 

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