T80495 |
MHuwentoxin-IV
|
|
98%
|
|
mHuwentoxin-IV, a naturally modified form of Huwentoxin-IV, selectively inhibits tetrodotoxin-sensitive (TTX-S) voltage-gated sodium channels in dorsal root gang...
|
T80499 |
Jingzhaotoxin XI
|
|
98%
|
|
Jingzhaotoxin XI (JZTX-XI) is a potent inhibitor of sodium conductance, exhibiting an IC50 value of 124 nM, and notably retards the rapid inactivation of Na_v1.5...
|
T80518 |
Mambalgin-3
|
|
98%
|
|
Mambalgin-3, an acid-sensitive ion channel 1 (ASIC1) inhibitor, has potential applications in analgesia research [1].
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T80519 |
M3-Huwentoxin IV
|
|
98%
|
|
m3-Huwentoxin IV (m3-HwTx-IV) is a potent inhibitor of sodium channels (NaV), exhibiting half-maximal inhibitory concentrations (IC50s) of 3.3 nM for hNaV1.7, 6....
|
T80533 |
Pterinotoxin-2
|
|
98%
|
|
Pterinotoxin-2 is a peptide toxin that acts as a sodium channel inhibitor [1].
|
T80534 |
Pterinotoxin-1
|
|
98%
|
|
Pterinotoxin-1 is a peptide toxin that functions as an inhibitor of sodium channels [1].
|
T81134 |
Sodium Channel inhibitor 4
|
587843-16-1
|
98%
|
|
Sodium Channel Inhibitor 4 is a compound that functions as a sodium channel inhibitor [1].
|
T82936 |
ATX-II TFA
|
|
98%
|
|
ATX-II TFA, a specific Na+ channel modulator toxin, is derived from the venom of the sea anemone (Anemonia sulcata). This compound impedes the inactivation of Na...
|
T22829 |
GX-674
|
1432913-36-4
|
98%
|
|
GX-674 is a highly potent and selective voltage-gated sodium channel 1.7 (Nav1.7) antagonist with an IC50 value of 0.1 nM measured at -40 mV for the study of inf...
|
TP1852 |
Myomodulin
|
110570-93-9
|
98%
|
|
Myomodulin is a neuropeptide present in molluscs, insects, and gastropods.Myomodulin is present in two identified aplysia neurons that contain myomodulin A the A...
|
TN4697 |
Odoroside H
|
18810-25-8
|
98%
|
|
Odoroside H has anticancer activities, the cytotoxic effects are induced by the inhibition of the plasma membrane bound Na(+)/K(+)-ATPase.
|
TN5141 |
Thevetin B
|
27127-79-3
|
98%
|
|
Thevetin B is a cardiac glycoside and an inhibitor of Na+-, K+-dependent adenosinetriphosphatase (Na+,K+-ATPase) from Thevetia peruviana.
|
TCA2511 |
11Beta-hydroxyprogesterone
|
600-57-7
|
98%
|
|
The progesterone derivatives 11 alpha- and 11 beta-hydroxyprogesterone are potent inhibitors of 11 beta-hydroxysteroid dehydrogenase (isoforms 1 and 2) in vitro ...
|
TN4276 |
Isocudraniaxanthone B
|
199851-52-0
|
98%
|
|
Isocudraniaxanthone B may have antimalarial activity.
|
T12951 |
Sodium Channel inhibitor 2
|
653573-60-5
|
98%
|
|
Sodium Channel inhibitor 2 is a blocker of sodium channel.
|
TN5234 |
Vindorosine
|
5231-60-7
|
98%
|
|
Vindorosine has blood vessel relaxation effect, possible underlying mechanisms involving the inhibition of Ca(2+) entry via L-type Ca(2+) channels in vascular sm...
|
TN2306 |
Wilfordine
|
37239-51-3
|
98%
|
|
Wilfordine is an insecticidally active alkaloid, Na+-K+-ATPase may be an acting target of wilfordine against some larvae of insect.
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T11239 |
Ethacizine hydrochloride
|
57530-40-2
|
98%
|
|
Ethacizine hydrochloride (NIK-244) has antiarrhythmic activity, and its effects are related to cardiac activity and can be used to study arrhythmias and myocardi...
|
TN5060 |
Stauntosaponin A
|
1417887-91-2
|
98%
|
|
Stauntosaponin A and stauntosaponin B show moderate inhibitory activities against Na+/K+-ATPase with IC50 values of 21 and 29 uM, respectively.
|
TN4183 |
Hardwickiic acid
|
1782-65-6
|
98%
|
|
Hardwickiic acid ((-)-Hardwikiic acid) is a natural compound derived from Pulicaria gnaphalodes and is an anti-injury receptor compound. hardwickiic acid blocks ...
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