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T1010 |
Verapamil hydrochloride
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Manidon,(±)-Verapamil hydrochlorid,Verapamil HCl,Calcan hydrochloride |
P450
,
Calcium Channel
,
P-gp
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Verapamil hydrochloride (Verapamil HCl) is a calcium channel blocker that is a class IV anti-arrhythmia agent. |
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T20656 |
Verapamil
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NSC 135784,NSC-135784,CP-16533-1,(±)-Verapamil |
P450
,
Calcium Channel
,
P-gp
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Verapamil (CP-16533-1) is a calcium channel blocker and an orally active and effective inhibitor of P-gp. Verapamil inhibits CYP3A4 and can be used in studies about the treatment of high blood pressure, heart arrhythmias... |
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T12646 |
(R)-Verapamil hydrochloride
|
(R)-(+)-Verapamil hydrochloride |
Others
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(R)-Verapamil hydrochloride ((R)-(+)-Verapamil hydrochloride) is a inhibitor of P-Glycoprotein. |
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T13879 |
(S)-Verapamil hydrochloride
|
(S)-(-)-Verapamil hydrochloride |
Calcium Channel
|
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(S)-Verapamil hydrochloride is an inhibitor of leukotriene C4 (LTC4) and calcein transport by MRP1,and leads to the death of potentially resistant tumor cells. |
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T40591 |
Verapamil EP Impurity C hydrochloride
|
NSC-609249 hydrochloride |
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NSC-609249 hydrochloride, an impurity of Verapamil, is a calcium channel blocker with potent orally active properties. It also functions as a first-generation P-glycoprotein (P-gp) inhibitor. |
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T11353 |
Gallopamil
|
Methoxyverapamil |
Calcium Channel
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TMIH-0002 |
(+/-)-Verapamil hydrochloride-d7
|
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(+/-)-Verapamil hydrochloride-d7 is a deuterated compound of (+/-)-Verapamil hydrochloride. (+/-)-Verapamil hydrochloride has a CAS number of 152-11-4. Verapamil hydrochloride is a calcium channel blocker that is a class... |
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T11353L |
Gallopamil hydrochloride
|
Methoxyverapamil hydrochloride |
Calcium Channel
|
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TMIH-0547 |
S-Verapamil-d7 HCL
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|
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S-Verapamil-d7 HCL is a deuterated compound of S-Verapamil HCL. S-Verapamil HCL has a CAS number of 1188265-55-5. |
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TMIH-0508 |
R-Verapamil-d7 HCL
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R-Verapamil-d7 HCL is a deuterated compound of R-Verapamil HCL. R-Verapamil HCL has a CAS number of 1188265-55-5. |
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T0563 |
Homoveratronitrile
|
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Others
|
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Homoveratronitrile is an impurity of Verapamil. It is also an intermediate in the preparation of the muscle relaxant Papverine. |
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T16339 |
Norverapamil hydrochloride
|
(±)-Norverapamil hydrochloride,D591 hydrochloride |
Calcium Channel
,
P-gp
,
Drug Metabolite
|
|
Norverapamil hydrochloride (D591 hydrochloride) ((±)-Norverapamil hydrochloride) is an N-demethylated metabolite of Verapamil and it is an L-type calcium channel blocker and a P-glycoprotein (P-gp) function inhibitor. |
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T30146 |
Arverapamil
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(R)-Norverapamil,Agi-003,UNII-3J8P56R04P,Rezular |
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Arverapamil is a chiral metabolite of Verapamil. |
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T26120 |
Ronipamil
|
Ronipamilo |
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Ronipamil is an analogue of verapamil that used as a calcium entry blocker. |
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T69956 |
KR30031
|
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KR30031 is a novel P-glycoprotein inhibitor with potential anticancer activity. KR30031 is a verapamil analog with fewer cardiovascular effects. The ability of KR-30031 to reduce this efflux transport is equal to that of... |
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T32912 |
Lu49888 HCl
|
Azidopamil,LU49888,LU 49888,Ludopamil,LU-49888 |
|
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LU 49888 is a photoaffinity analog of verapamil that has been used to identify specific binding sites for phenylalkylamines of calcium channels present in rabbit skeletal muscle microsomes. |
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T69317 |
Dexverapamil
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|
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Dexverapamil is the R-enantiomer of the calcium channel blocker verapamil. Dexverapamil competitively inhibits the multidrug resistance efflux pump P-glycoprotein (MDR-1), thereby potentially increasing the effectiveness... |
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T27302 |
Falipamil
|
AQ-A 39,AQ-A-39,AQ-A39 |
|
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Falipamil is a verapamil derivative and a calcium channel antagonist. Falipamil exerts antitachycardic effects by a direct action on the sinus node. Falipamil decreases HR at exercise in normal subjects and may exert ant... |
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TMIH-0399 |
Norverapamil-d7 HCl
|
|
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Norverapamil-d7 HCl is a deuterated compound of Norverapamil HCl. Norverapamil HCl has a CAS number of 67812-42-4. Norverapamil hydrochloride ((±)-Norverapamil hydrochloride) is an N-demethylated metabolite of Verapamil ... |
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T35568 |
BODIPY-aminoacetaldehyde diethyl acetal
|
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BODIPY-aminoacetaldehyde diethyl acetal (BAAA-DA) is a stable precursor to BODIPY-aminoacetaldehyde, a cell-permeable fluorescent substrate for aldehyde dehydrogenase (ALDH).1,2BODIPY-aminoacetaldehyde diethyl acetal is ... |
