28 Results for "

N-type calcium channel

" in MedChemExpress (MCE) Product Catalog:
Products (28)

28 Results for "N-type calcium channel" in MCE Product Catalog:

3
3 Cited Publications
Cat. No.: HY-103318
CAS No.: 217171-01-2
Purity:  99.88%
Target:  

Calcium Channel

Research Areas:  

Neurological Disease

PD173212 is a selective N-type voltage sensitive calcium channel (VSCC) blocker, with an IC50 of 36 nM in IMR-32 assays.
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2
2 Cited Publications
Cat. No.: HY-P0062B
CAS No.: 914454-03-8
Synonyms: SNX-111 acetate
Ziconotide acetate (SNX-111 acetate), a peptide, is a potent and selective block of N-type calcium channels antagonist. Ziconotide acetate reduces synaptic transmission, and can be used for chronic pain research .
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2
2 Cited Publications
Cat. No.: HY-103309
CAS No.: 1346233-68-8
Purity:  99.49%
Target:  

Calcium Channel

Research Areas:  

Neurological Disease

ML218 is a potent, selective and orally active T-type Ca 2+ channels (Cav3.1, Cav3.2, Cav3.3) inhibitor with IC50s of 310 nM and 270 nM for Cav3.2 and Cav3.3, respectively. ML218 inhibits the burst activity in subthalamic nucleus (STN) neurons. ML218 has no significant inhibition of L- or N-type calcium channels, KATP or hERG potassium channels. ML218 can penetrate the blood-brain barrier .
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1
1 Cited Publications
Cat. No.: HY-119373
CAS No.: 1567335-29-8
Purity:  98.78%
Target:  

Calcium Channel

Research Areas:  

Neurological Disease

Cav 2.2 blocker 1 (compound 9) is a N-type calcium channel (Cav 2.2) blocker for the treatment of pain, with an IC50 of 1 nM .
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Cat. No.: HY-P0062
CAS No.: 107452-89-1
Synonyms: SNX-111
Ziconotide (SNX-111), a peptide, is a potent and selective block of N-type calcium channels antagonist. Ziconotide reduces synaptic transmission, and can be used for chronic pain research .
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Cat. No.: HY-120751
CAS No.: 1309601-26-0
Target:  

Calcium Channel

Research Areas:  

Neurological Disease

TROX-1 is a selective, orally active and brain-penetrant N-type calcium channel (Cav2.2) inhibitor with an IC50 value of 0.11 μM. TROX-1 exerts state-dependent and use-dependent inhibition, preferentially targets open/inactivated channels, blocks depolarization-associated calcium influx, and fully blocks calcium influx in rat dorsal root ganglion neurons. TROX-1 reverses inflammatory-induced hyperalgesia, nerve injury-induced allodynia. TROX-1 can be used for the research of pain .
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Cat. No.: HY-14462
CAS No.: 41332-24-5
Purity:  98.73%
Synonyms: 39-1B4
Target:  

Calcium Channel

Research Areas:  

Cardiovascular Disease

NP118809 is a potent N-type calcium channel blocker, with an IC50 of 0.11 μM; also less potently inhibits L-type calcium channel with an IC50 of 12.2 μM.
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Cat. No.: HY-100310
CAS No.: 241499-17-2
Target:  

Calcium Channel

Research Areas:  

Neurological Disease

N-type calcium channel blocker-1 is an orally active compound which shows high affinity to functionally block N-type calcium channels with an IC50 of 0.7 μM in the IMR32 assay.
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Cat. No.: HY-P1079
CAS No.: 158484-42-5
Target:  

Calcium Channel

Research Areas:  

Neurological Disease

ω-Agatoxin TK, a peptidyl toxin of the venom of Agelenopsis aperta, is a potent and selective P/Q type Ca 2+ channel blocker. ω-Agatoxin TK inhibits the high K + depolarisation-induced rise in internal Ca 2+ in cerebral isolated nerve endings with an IC50 of of 60 nM. ω-Agatoxin TK has no effect on L-type, N-type, or T-type calcium channels .
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Cat. No.: HY-147638
CAS No.: 1909225-94-0
Purity:  99.18%
Target:  

Calcium Channel

Research Areas:  

Neurological Disease

MONIRO-1 is a T-type and N-type calcium channel blocker with IC50 values of 34, 3.3, 1.7 and 7.2 µM against hCav2.2, hCav3.1, hCav3.2 and hCav3.3, respectively. MONIRO-1 has low activity against L-type calcium channels. MONIRO-1 can be used for the study of pain and epilepsy .
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Cat. No.: HY-U00236
CAS No.: 248922-46-5
Target:  

Calcium Channel

Research Areas:  

Cardiovascular Disease

PD0176078 is a newly found N-type Calcium channel blocker.
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Cat. No.: HY-105365
CAS No.: 217170-95-1
Target:  

Calcium Channel

Research Areas:  

Neurological Disease

PD 175069 is a potent and selective N-type calcium channel antagonist with an IC50 of 0.32 μM. PD 175069 is efficacious in an audiogenic seizure model using DBA/2 mice. PD 175069 can be used for research on neurological conditions such as neuropathic pain and stroke .
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Cat. No.: HY-126336
CAS No.: 2376051-91-9
HM12 is a covalent inhibitor of L-/T-type calcium channels. HM12 can strongly inhibit the Cav1.2 (L-type) and Cav3.2 (T-type) calcium channels, and has selectivity for the N-type channels. HM12 produces an irreversible inhibition that persisted after washout. HM12 can be used to study diseases such as hypertension, pain, epilepsy, etc .
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Cat. No.: HY-P0062A
Synonyms: SNX-111 TFA
Ziconotide TFA (SNX-111 TFA), a peptide, is a potent and selective block of N-type calcium channels antagonist. Ziconotide TFA reduces synaptic transmission, and can be used for chronic pain research .
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Cat. No.: HY-120484
CAS No.: 1219624-62-0
Target:  

Calcium Channel

Research Areas:  

Neurological Disease

A-1048400 is an orally active and selective calcium channel inhibitor with an IC50 value of 1.4 μM for N-type channels, 1.2 μM for T-type channel. A-1048400 inhibits neurotransmitter release and reduces membrane hyperexcitability, exerting potent analgesic activity. A-1048400 is promising for research of neuropathic pain (e.g., pain induced by spinal nerve ligation and chronic constriction injury) .
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Cat. No.: HY-P1078
CAS No.: 1600543-88-1
Target:  

Calcium Channel

Research Areas:  

Neurological Disease

Huwentoxin XVI, an analgesic, is a highly reversible and selective mammalian N-type calcium channel (IC50 of ~60 nM) antagonist from Chinese tarantula Ornithoctonus huwena. Huwentoxin XVI has no effect on voltagegated T-type calcium channels, potassium channels or sodium channels .
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Cat. No.: HY-P1078A
Target:  

Calcium Channel

Research Areas:  

Neurological Disease

Huwentoxin XVI TFA, an analgesic, is a highly reversible and selective mammalian N-type calcium channel (IC50 of ~60 nM) antagonist from Chinese tarantula Ornithoctonus huwena. Huwentoxin XVI TFA has no effect on voltagegated T-type calcium channels, potassium channels or sodium channels .
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Cat. No.: HY-P5179
CAS No.: 769973-37-7
Synonyms: HWTX-I
Research Areas:  

Neurological Disease

Huwentoxin I (HWTX-I) is a peptide toxin that inhibits voltage-gated sodium channels and N-type calcium channels. Huwentoxin I inhibits sodium channels in rat hippocampus and cockroach dorsal unpaired median (DUM) neurons with IC50 values of 66.1 and 4.80 nM, respectively .
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Cat. No.: HY-118974
CAS No.: 225925-12-2
Target:  

Calcium Channel

Research Areas:  

Neurological Disease Cancer

PD-151307 is an N-type calcium channel antagonist with significant inhibitory effects in IMR-32 human neuroblastoma cells, exhibiting an IC50 of 0.32 µM. PD-151307 can be used in research related to cancer therapy, anticonvulsants, and neuropathic pain .
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Cat. No.: HY-P2699
CAS No.: 152617-90-8
Synonyms: GrTx; ω-GsTx SIA
Target:  

Calcium Channel

Research Areas:  

Neurological Disease

ω-Grammotoxin SIA (GrTx) is P/Q and N-type voltage-gated Calcium channels inhibitor. ω-Grammotoxin SIA is also a protein toxin that can be obtained from spider venom. ω-Grammotoxin SIA has the potential to study neurological diseases as well as cardiovascular diseases .
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