Proteins > Voltage-dependent L-type calcium channel subunit alpha-1D
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Voltage-dependent L-type calcium channel subunit alpha-1D
A voltage-dependent L-type calcium channel subunit alpha-1D that is encoded in the genome of rat. [OMA:P27732, PRO:DNx]
Synonyms
Calcium channel, L type, alpha-1 polypeptide, isoform 2;
Rat brain class D;
RBD;
Voltage-gated calcium channel subunit alpha Cav1.3
Research
Bioassay Publications (17)
| Timeframe | Studies on this Protein(%) | All Drugs % |
|---|
| pre-1990 | 1 (5.88) | 18.7374 |
| 1990's | 5 (29.41) | 18.2507 |
| 2000's | 3 (17.65) | 29.6817 |
| 2010's | 8 (47.06) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
Compounds (21)
Drugs with Inhibition Measurements
| Drug | Taxonomy | Measurement | Average (mM) | Bioassay(s) | Publication(s) |
|---|
| gallopamil | Rattus norvegicus (Norway rat) | IC50 | 0.0230 | 1 | 1 |
| carbinoxamine | Rattus norvegicus (Norway rat) | Ki | 1.0800 | 1 | 1 |
| isradipine | Rattus norvegicus (Norway rat) | IC50 | 0.2210 | 1 | 1 |
| nicardipine | Rattus norvegicus (Norway rat) | Ki | 0.0008 | 1 | 1 |
| nifedipine | Rattus norvegicus (Norway rat) | Ki | 0.0039 | 2 | 3 |
| nitrendipine | Rattus norvegicus (Norway rat) | IC50 | 0.0013 | 1 | 1 |
| ondansetron | Rattus norvegicus (Norway rat) | Ki | 10.0000 | 2 | 3 |
| dexpropranolol | Rattus norvegicus (Norway rat) | Ki | 14.5000 | 1 | 1 |
| diltiazem | Rattus norvegicus (Norway rat) | IC50 | 0.8960 | 3 | 3 |
| diltiazem | Rattus norvegicus (Norway rat) | Ki | 0.0585 | 2 | 2 |
| ryodipine | Rattus norvegicus (Norway rat) | IC50 | 6,000,000.0000 | 1 | 3 |
| fr 7534 | Rattus norvegicus (Norway rat) | IC50 | 0.0450 | 1 | 1 |
| eplerenone | Rattus norvegicus (Norway rat) | IC50 | 5.0000 | 1 | 1 |
| curcumin | Rattus norvegicus (Norway rat) | IC50 | 100.0000 | 1 | 1 |
| pranidipine | Rattus norvegicus (Norway rat) | IC50 | 0.0370 | 1 | 1 |
| dexniguldipine | Rattus norvegicus (Norway rat) | Ki | 0.0597 | 1 | 1 |
| cilansetron | Rattus norvegicus (Norway rat) | Ki | 8.4667 | 2 | 3 |
| mebudipine | Rattus norvegicus (Norway rat) | IC50 | 0.0200 | 1 | 1 |
| sb-435495 | Rattus norvegicus (Norway rat) | IC50 | 10.0000 | 1 | 1 |
| nitd 609 | Rattus norvegicus (Norway rat) | IC50 | 10.0000 | 1 | 1 |
| XL413 | Rattus norvegicus (Norway rat) | IC50 | 28.4500 | 2 | 2 |
Drugs with Other Measurements
| Drug | Taxonomy | Measurement | Average (mM) | Bioassay(s) | Publication(s) |
|---|
| bay-k-8644 | Rattus norvegicus (Norway rat) | Concentration | 3.0000 | 1 | 1 |
A homologous series of permanently charged 1,4-dihydropyridines: novel probes designed to localize drug binding sites on ion channels.Journal of medicinal chemistry, , Nov-12, Volume: 36, Issue:23, 1993
Stereoselectivity of a potent calcium antagonist, 1-benzyl-3-pyrrolidinyl methyl 2,6-dimethyl-4-(m-nitrophenyl)-1,4-dihydropyridine-3,5-dicarboxylate.Journal of medicinal chemistry, , Volume: 29, Issue:12, 1986
Cinnamides as selective small-molecule inhibitors of a cellular model of breast cancer stem cells.Bioorganic & medicinal chemistry letters, , Mar-15, Volume: 23, Issue:6, 2013
Discovery of {1-[4-(2-{hexahydropyrrolo[3,4-c]pyrrol-2(1H)-yl}-1H-benzimidazol-1-yl)piperidin-1-yl]cyclooctyl}methanol, systemically potent novel non-peptide agonist of nociceptin/orphanin FQ receptor as analgesic for the treatment of neuropathic pain: deBioorganic & medicinal chemistry, , Nov-01, Volume: 18, Issue:21, 2010
L-Type calcium channel blockers: from diltiazem to 1,2,4-oxadiazol-5-ones via thiazinooxadiazol-3-one derivatives.Journal of medicinal chemistry, , Apr-23, Volume: 52, Issue:8, 2009