6 Results for "

Sodium Channel-IN-7

" in MedChemExpress (MCE) Product Catalog:
Products (6)

6 Results for "Sodium Channel-IN-7" in MCE Product Catalog:

Cat. No.: HY-185333
CAS No.: 2914907-77-8
Target:  

Sodium Channel

Research Areas:  

Neurological Disease

Sodium Channel-IN-7 (Example 59) is a NaV1.7 voltage-gated sodium channel inhibitor.Sodium Channel-IN-7 binds to the VSD4 binding pocket of NaV1.7, with reduced interaction with Try1537.Sodium Channel-IN-7 can be used for the research of pain .
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Cat. No.: HY-123825
CAS No.: 1432913-36-4
GX-674 is a potent, state-dependent, isoform-selective voltage-gated sodium channel 1.7 (Nav1.7) antagonist with an IC50 of 0.1 nM at -40 mV .
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Cat. No.: HY-P5925A
Synonyms: SsTx ToxIN TFA
Ssm Spooky Toxin TFA is found in Scolopendra mutilans that potently inhibits KCNQ (voltage-gated potassium channel family 7) channels, with IC50s of 2.8 μM, 5.26 μM and 0.1-0.3 M for Kv7.4, Kv1.3, and Shal channel, respectivily. Ssm Spooky Toxin TFA inhibits cytokine generation by specifically acting on the KV1.3 channel in T cells. Ssm Spooky Toxin TFA plays an essential role in the centipede’s circulatory system .
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Cat. No.: HY-115823
CAS No.: 325457-98-5
Target:  

Potassium Channel

Research Areas:  

Neurological Disease

ztz240 is a chemical modulator of voltage-gated potassium channel Kv7 (KCNQ) (KCNQ2 and 3: EC50=6.1 μM; KCNQ4: EC50=12.2 μM). ztz240 can be used in analgesia and anti-epileptic research .
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Cat. No.: HY-P5925
Synonyms: SsTx ToxIN
Ssm Spooky Toxin is found in Scolopendra mutilans that potently inhibits KCNQ (voltage-gated potassium channel family 7) channels, with IC50s of 2.8 μM, 5.26 μM and 0.1-0.3 M for Kv7.4, Kv1.3, and Shal channel, respectivily. Ssm Spooky Toxin inhibits cytokine generation by specifically acting on the KV1.3 channel in T cells. Ssm Spooky Toxin plays an essential role in the centipede’s circulatory system .
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Cat. No.: HY-184393
CAS No.: 687569-15-9
Target:  

Calcium Channel

Research Areas:  

Neurological Disease

Calcium Channel antagonist 7 (Compound 298) is a voltage-gated calcium channel antagonist, with its IC50 ranging from 5 to 20 μM. Calcium Channel antagonist 7 can be used for researching diseases such as pain .
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