202

Rosiglitazone maleate

202 Publications Verification

Cat. No.: HY-14600

CAS No.: 155141-29-0

Purity: 99.73%

Synonyms: BRL 49653C

Target:

PPAR TRP Channel Autophagy Ferroptosis

Research Areas:

Metabolic Disease Inflammation/Immunology Cancer

Rosiglitazone maleate (BRL 49653C) is a potent and selective activator of PPARγ, with EC₅₀s of 30 nM, 100 nM and 60 nM for PPARγ1, PPARγ2, and PPARγ, respectively, and a K_d of appr 40 nM for PPARγ; Rosiglitazone maleate is also an modulator of TRP channels, inhibits TRP melastatin 2 (TRPM2), TRPM3 and activates TRP canonical 5 (TRPC5).

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139

GsMTx4

139 Cited Publications

Cat. No.: HY-P1410

CAS No.: 1209500-46-8

Target:

TRP Channel Piezo Channel

Research Areas:

Cardiovascular Disease Neurological Disease Inflammation/Immunology

GsMTx4 is a spider venom peptide that selectively inhibits cationic-permeable mechanosensitive channels (MSCs) belonging to the Piezo and TRP channel families. GsMTx4 also blocks cation-selective stretch-activated channels (SACs) , attenuates lysophosphatidylcholine (LPC)-induced astrocyte toxicity and microglial reactivity. GsMTx4 is an important pharmacological tool for identifying the role of these excitatory MSCs in normal physiology and pathology .

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139

GsMTx4 TFA

139 Cited Publications

Cat. No.: HY-P1410A

Target:

TRP Channel Piezo Channel

Research Areas:

Cardiovascular Disease Neurological Disease Inflammation/Immunology

GsMTx4 TFA is a spider venom peptide that selectively inhibits cationic-permeable mechanosensitive channels (MSCs) belonging to the Piezo and TRP channel families. GsMTx4 TFA also blocks cation-selective stretch-activated channels (SACs) , attenuates lysophosphatidylcholine (LPC)-induced astrocyte toxicity and microglial reactivity. GsMTx4 TFA is an important pharmacological tool for identifying the role of these excitatory MSCs in normal physiology and pathology .

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85

2-Aminoethyl diphenylborinate

85 Cited Publications

Cat. No.: HY-W009724

CAS No.: 524-95-8

Synonyms: 2-APB

Target:

Calcium Channel TRP Channel CRAC Channel

Research Areas:

Cardiovascular Disease Inflammation/Immunology

2-Aminoethyl diphenylborinate (2-APB) is a cell-permeable inhibitor of Inositol triphosphate receptor (IP3R). 2-Aminoethyl diphenylborinate also inhibits the store-operated Ca ²⁺ (SOC) channel and activates some TRP channels (V1, V2 and V3). Additionally, 2-Aminoethyl diphenylborinate has inhibitory effects on vasospasm. At high concentrations, it exhibits specific anti-inflammatory and antioxidant effects in neural tissue .

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8

(E/Z)-BML264

8 Cited Publications

Cat. No.: HY-118628

CAS No.: 110683-10-8

Purity: 99.63%

Synonyms: N-(p-Amylcinnamoyl) anthranilic acid; ACA

Target:

Phospholipase TRP Channel

Research Areas:

Cardiovascular Disease

(E/Z)-BML264 (N-(p-amylcinnamoyl) Anthranilic Acid) is a broad spectrum Phospholipase A₂ (PLA₂) inhibitor and TRP channel blocker . (E/Z)-BML264 is a SLC13A3 inhibitor. (E/Z)-BML264 (N-(p-amylcinnamoyl) Anthranilic Acid) is also an effective reversible inhibitor of calcium-activated chloride channels, has potential to treat arrhythmia .

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8

ML204

8 Cited Publications

Cat. No.: HY-12949

CAS No.: 5465-86-1

Purity: 98.45%

Target:

TRP Channel

Research Areas:

Neurological Disease

ML204 is a potent, selective TRPC4/TRPC5 channel inhibitor, with at least 19-fold selectivity against TRPC6 and no appreciable effect on all other TRP channels, nor on voltage-gated sodium, potassium, or Ca ²⁺ channels .

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8

ML204 hydrochloride

8 Cited Publications

Cat. No.: HY-12949A

CAS No.: 2070015-10-8

Purity: 99.74%

Target:

TRP Channel

Research Areas:

Neurological Disease

ML204 hydrochloride is a novel, potent, selective TRPC4/TRPC5 channel inhibitor, with at least 19-fold selectivity against TRPC6 and no appreciable effect on all other TRP channels, nor on voltage-gated sodium, potassium, or Ca ²⁺ channels .

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3

Pyr10

3 Cited Publications

Cat. No.: HY-19408

CAS No.: 1315323-00-2

Target:

TRP Channel

Research Areas:

Others

Pyr10 is a pyrazole derivative and a selective TRP cation 3 (TRPC3) inhibitor. Pyr10 inhibits Ca ²⁺ influx in carbachol-stimulated TRPC3-transfected HEK293 cells with an IC₅₀ of 0.72 μM (IC₅₀ of 13.08 μM for store operated Ca ²⁺ entry in BRL-2H3 cells). Pyr10 has the ability to distinguish between receptor-operated TRPC3 and native stromal interaction molecule 1 (STIM1)/Orai1 channels .

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