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AB144622

ML-SA1, TRPML agonist

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(3 Publications)

MW 362.4 Da, Purity >98%. Selective TRPML agonist. Induces TRPML1, 2 and 3-mediated Ca2+ release from lysosomes in vitro. Does not activate TRPM2, TRPV2, TRPA1, TRPV3, TRPC6 channels. Cell-permeable.

View Alternative Names

CCE1, CRF 2, CRF 2R, CRF BP, CRF RB, CRF binding protein, CRF2 receptor beta isoform, CRFR2_HUMAN, CRH 2R, Corticotropin releasing factor binding protein, Corticotropin releasing hormone binding protein, Corticotropin-releasing factor receptor 2, Corticotropin-releasing hormone receptor 2, HM CRF, MGC119570, MGC119571, MGC119572, MGC119573, RP11-10M8.1, STRPC4, Short transient receptor potential channel 4, TRP 4, TRPC 4, TRPC4 protein, TRPC4_HUMAN, Transient receptor potential 4, Transient receptor potential cation channel subfamily C member 4, Trp-related protein 4, corticotropin releasing factor receptor, hTrp-4, transient receptor potential cation channel subfamily C, transient receptor potential channel 4

1 Images
Chemical Structure - ML-SA1, TRPML agonist (AB144622)
  • Chemical Structure

Lab

Chemical Structure - ML-SA1, TRPML agonist (AB144622)

2D chemical structure image of ab144622, ML-SA1, TRPML agonist

Key facts

CAS number

332382-54-4

Purity

>98%

Form

Solid

form

Molecular weight

362.4 Da

Molecular formula

C<sub>2</sub><sub>2</sub>H<sub>2</sub><sub>2</sub>N<sub>2</sub>O<sub>3</sub>

PubChem

2880983

Nature

Synthetic

Solubility

Soluble in ethanol to 10 mM

Soluble in DMSO to 50 mM

Biochemical name

2-[2-oxo-2-(2,2,4-trimethyl-3,4-dihydroquinolin-1(2H)-yl)ethyl]-1H-isoindole-1,3(2H)-dione

Biological description

Selective TRPML agonist. Induces TRPML1, 2 and 3-mediated Ca2+ release from lysosomes in vitro. Does not activate TRPM2, TRPV2, TRPA1, TRPV3, TRPC6 channels. Cell-permeable.

Canonical smiles

CC1CC(N(C2=CC=CC=C12)C(=O)CN3C(=O)C4=CC=CC=C4C3=O)(C)C

InChi

InChI=1S/C22H22N2O3/c1-14-12-22(2,3)24(18-11-7-6-8-15(14)18)19(25)13-23-20(26)16-9-4-5-10-17(16)21(23)27/h4-11,14H,12-13H2,1-3H3

InChiKey

KDDHBJICVBONAX-UHFFFAOYSA-N

IUPAC Name

2-[2-oxo-2-(2,2,4-trimethyl-3,4-dihydroquinolin-1-yl)ethyl]isoindole-1,3-dione

Properties and storage information

Shipped at conditions
Ambient - Can Ship with Ice
Appropriate short-term storage conditions
+4°C
Appropriate long-term storage conditions
+4°C
Storage information
The product can be stored for up to 12 months

Supplementary information

This supplementary information is collated from multiple sources and compiled automatically.

TRPC4 also known as Transient Receptor Potential Cation Channel Subfamily C Member 4 plays an important mechanical role as a non-selective cation channel that conducts calcium and sodium ions into cells. This protein has a molecular weight of approximately 100 kDa. TRPC4 is highly expressed in various tissues including the brain heart lung and kidney. Its presence in these tissues suggests an important role in multiple physiological processes.
Biological function summary

TRPC4 influences cellular calcium signaling impacting a variety of physiological responses such as vasodilation and neurotransmission. TRPC4 can form both homo- and heteromeric complexes often associating with other TRPC family members. Through these complexes TRPC4 contributes to cellular responses to neurotransmitters and other signaling molecules indicating its role in a wide range of cellular functions.

Pathways

TRPC4 participates in the phospholipase C (PLC) signaling pathway which regulates important cellular functions such as cell proliferation and differentiation. TRPC4 is related to G-protein coupled receptors (GPCRs) within this pathway facilitating the relay of extracellular signals through PLC activation and subsequent calcium influx. Additionally TRPC4 interacts with proteins like calmodulin which modulates its activity and impacts calcium-related signaling pathways.

TRPC4's dysregulation associates with cardiovascular diseases and anxiety disorders. The aberrant calcium entry through TRPC4 channels can lead to pathological conditions such as hypertension and heart failure. During stress responses the interaction between TRPC4 and CRHR2 the corticotropin-releasing hormone receptor 2 may affect anxiety-related behaviors hinting at TRPC4’s involvement in psychiatric disorders. By influencing these pathways TRPC4 emerges as a potential therapeutic target for managing such conditions.

Product protocols

Publications (3)

Recent publications for all applications. Explore the full list and refine your search

Traffic (Copenhagen, Denmark) 24:334-354 PubMed37218497

2023

Deacidification of endolysosomes by neuronal aging drives synapse loss.

Applications

Unspecified application

Species

Unspecified reactive species

Tatiana Burrinha,César Cunha,Michael J Hall,Mafalda Lopes-da-Silva,Miguel C Seabra,Cláudia Guimas Almeida

Autophagy 16:1683-1696 PubMed31826695

2019

Oxidation of multiple MiT/TFE transcription factors links oxidative stress to transcriptional control of autophagy and lysosome biogenesis.

Applications

Unspecified application

Species

Unspecified reactive species

Hongfeng Wang,Nana Wang,Delai Xu,Qilian Ma,Yang Chen,Shiqiang Xu,Qin Xia,Yan Zhang,Jochen H M Prehn,Guanghui Wang,Zheng Ying

Oxidative medicine and cellular longevity 2018:4612727 PubMed30662583

2018

Degradation of TRPML1 in Neurons Reduces Neuron Survival in Transient Global Cerebral Ischemia.

Applications

Unspecified application

Species

Unspecified reactive species

Yang Wang,Shao-Wei Jiang,Xuan Liu,Lei Niu,Xiao-Li Ge,Jin-Cheng Zhang,Hai-Rong Wang,Ai-Hua Fei,Cheng-Jin Gao,Shu-Ming Pan
View all publications

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