| Structure | Cat No. | Product Name | CAS No. | Product Description |
|---|---|---|---|---|
|
V71512 | (-)-Denudatin B (Denudatin B) | 87402-88-8 | (-)-Denudatin B has antiplatelet effects and inhibits Ca2+ influx through voltage-gated and receptor-regulated Ca2+ channels, thereby relaxing vascular smooth muscle. |
|
V121434 | (2R,3R)-Diltiazem hydrochloride | 42399-54-2 | (2R,3R)-Diltiazem hydrochloride is an isomer of diltiazem hydrochloride. |
|
V96761 | (rel)-Mirogabalin | 1138244-97-9 | (rel)-Mirogabalin ((rel)-DS5565) is a voltage-dependent calcium channel inhibitor targeting the α2δ-1 subunit. |
|
V4179 | (S)-(-)-Bay-K-8644 | 98625-26-4 | S)-(-)-Bay-K-8644, the S-enantiomer ofBay-K-8644,is a novel and potent Ca2+ channel activator that activates Ba2+currents (IBa) with an EC50of 32 nM. |
|
V123631 | 1-Myristyl-2-hydroxy-sn-glycero-3-PA | 1-Myristyl-2-hydroxy-sn-glycero-3-PA is a derivative of lysophosphatidic acid. | |
|
V127657 | 8-[2-(3-Methylbutroxy)-3-hydroxy-3-methylbutoxy]psoralen | 68006-84-8 | 8-[2-(3-Methylbutroxy)-3-hydroxy-3-methylbutoxy]psoralen is a furanocoumarin found in the roots of Angelica archangelica L. archangelica, and is a calcium antagonist. |
|
V101510 | 8-Br-7-CH-cADPR | 189876-06-0 | 8-Br-7-CH-cADPR (7-Deaza-8-bromo-cADPR) is a potent cADPR antagonist. |
|
V2931 | ABT-639 | 1235560-28-7 | ABT-639 is a new potent, peripherally acting, selective T-type Ca2+channel blocker that blocks recombinant human T-type (Cav3.2) Ca2+channels in a voltage-dependent fashion (IC50=2 μM) and attenuates low voltage-activated (LVA) currents in rat DRG neurons (IC50=8 μM). |
|
V1687 | AMG-517 | 659730-32-2 | AMG 517 (AMG-517; AMG517) is a novel, potent and selective TRPV1 (vanilloid receptor-1) antagonist with potential anti-inflammatory activity. |
|
V78345 | Barnidipine-d5 hydrochloride (Mepirodipine-d5 hydrochloride; YM-09730-5-d5 hydrochloride) | Barnidipine-d5 ( HCl) is the deuterated form of Barnidipine HCl. | |
|
V1708 | Betamethasone (NSC-39470; SCH-4831) | 378-44-9 | Betamethasone (also called NSC-39470; SCH-4831;NSC39470; SCH4831)is a glucocorticoid steroid and an approved medication with moderateanti-inflammatory and immunosuppressive activities. |
|
V71495 | Calcium Channel antagonist 4 | 687574-49-8 | Calcium Channelantagonist 4 (compound 189) is a voltage-gated calcium channel inhibitor (antagonist) with IC50 of 5-20μM. |
|
V71524 | Cav 3.2 inhibitor 4 | 1416984-93-4 | Cav 3.2 inhibitor 4 (compound 21) is a potent, peripherally restricted and selective T-type calcium channel (Cav3.2) inhibitor (antagonist) with IC50 of 0.6 μM. |
|
V1693 | CFTRinh-172 | 307510-92-5 | CFTRinh-172 (also known as CFTR Inhibitor172;CFTR-Inh 172; CFTR inhibitor 172)is a potent, voltage-independent, and selective inhibitor of CFTR (Cystic fibrosis transmembrane conductance regulator) with potential anti-fibrotic and anti-diarrhea effects. |
|
V131715 | Cimicifugic acid D | 219986-51-3 | Cimicifugic acid D is a benzyl tartrate that induces vasodilation in preconstricted rat aortic strips and initiates an endothelial-independent vasodilation mechanism. |
|
V71483 | Crisugabalin (HSK16149) | 2209104-84-5 | Crisugabalin (HSK16149) is a novel voltage-gated calcium channel (VGCC) α2δ subunit ligand. |
|
V120324 | D-myo-Inositol-1,2,6-triphosphate sodium | D-inositol-1,2,6-triphosphate (sodium) is a member of the inositol phosphate second messenger family and plays an important role in cell signaling. | |
|
V107785 | D-myo-Inositol-1,2-diphosphate sodium | 208584-51-4 | Sodium D-inositol-1,2-bisphosphate (Ins(1,2)P2) is one of the many inositol phosphate (InsP) isomers that act as a small, soluble second messenger in cell signaling. |
|
V106463 | Devapamil | 92302-55-1 | Devapamil (D 888; demethoxyverapamil) is a calcium channel blocker. |
|
V71537 | Diltiazem-(acetoxy-d3) (hydrochloride) | 1217860-13-3 | Diltiazem-(acetoxy-d3) ( HCl) is the deuterated form of Diltiazem HCl. |