santa cruz biotechnology, inc.

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| | Sigma Receptors and Sigma Ligands
- 4-IBP
Combines high affinity for σ 1 and moderate affinity for σ 2 sites. Centrally active following systemic administration in vivo.| Katalog # | CAS Nummer | Summenformel | Menge |
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| sc-203779 | 155798-12-2 | C19H21IN2O | 10 mg/50 mg |
- BD 1008
Potent and selective σ-ligand.| Katalog # | CAS Nummer | Summenformel | Menge |
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| sc-203426 | 138356-08-8 | C15H22Cl2N2 | 10 mg/50 mg |
- BD 1047 dihydrobromide
A selective antagonist of σ receptors.| Katalog # | CAS Nummer | Summenformel | Menge |
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| sc-203837 | 138356-20-4 | C13H20CI2N2 ·2HBr | 10 mg/50 mg |
- BD 1063 dihydrochloride
A selective antagonist of the σ receptors.| Katalog # | CAS Nummer | Summenformel | Menge |
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| sc-203838 | 150208-28-9 | C13H18Cl2N2 ·2HCl | 10 mg/50 mg |
- BMY 14802 hydrochloride
| Katalog # | CAS Nummer | Summenformel | Menge |
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| sc-361126 | 105565-55-7 | C18H22F2N4O.HCl | 10 mg/50 mg |
- Carbetapentane citrate
| Katalog # | CAS Nummer | Summenformel | Menge |
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| sc-203538 | 23142-01-0 | C20H31NO3 ·C6H8O7 | 100 mg |
- Carbetapentane
A non-opioid sigma site agonist, antitussive and anticonvulsant. Demonstrates neuroprotection against excitotoxicity.| Katalog # | CAS Nummer | Summenformel | Menge |
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| sc-201100 | 77-23-6 | C20H31NO3 | 100 mg/500 mg |
- DTG
| Katalog # | CAS Nummer | Summenformel | Menge |
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| sc-203332 | 97-39-2 | C15H17N3 | 1 g |
- (+)-Igmesine hydrochloride
| Katalog # | CAS Nummer | Summenformel | Menge |
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| sc-362749 | 130152-35-1 | C23H29CN.HCl | 10 mg/50 mg |
- IPAG
Potent σ-receptor antagonist.| Katalog # | CAS Nummer | Summenformel | Menge |
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| sc-204017 | n.n. | C17H22IN3 | 10 mg/50 mg |
- L-693,403 maleate
| Katalog # | CAS Nummer | Summenformel | Menge |
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| sc-361222 | 137730-52-0 | C20H23N.C4H4O4 | 10 mg/50 mg |
- METAPHIT
Acylator of PCP and σ-receptors.| Katalog # | CAS Nummer | Summenformel | Menge |
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| sc-204078 | 96316-00-6 | C18H24N2S | 10 mg/50 mg |
- N-[2-(Piperidinylamino)ethyl]-4-iodobenzamide
σ-1 selective ligand which binds with high affinity to human malignant melanoma cells A 2058.| Katalog # | CAS Nummer | Summenformel | Menge |
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| sc-204110 | n.n. | C14H19IN2O | 10 mg/50 mg |
- NE 100 hydrochloride
Potent, selective σ1 receptor antagonist (Ki = 0.86 nM) that displays > 55 fold selectivity over σ2 receptors and > 6000 fold selectivity over D1, D2, 5-HT1A, 5-HT2 and PCP receptors. Exhibits reversible binding (Kd = 1.2 nM) and displays antipsychotic activity in vivo. Orally active.| Katalog # | CAS Nummer | Summenformel | Menge |
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| sc-204121 | 149409-57-4 | C23H33NO2 ·HCl | 10 mg/50 mg |
- PB 28 dihydrochloride
| Katalog # | CAS Nummer | Summenformel | Menge |
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| sc-204834 | 172906-90-0 | C24H38N2O•2HCl | 10 mg/50 mg |
- PD 144418 oxalate
Selective σ1 ligand displaying high selectivity. Exhibits no other significant activity at a wide range of other receptors, ion channels, and enzumes. Following i.p. administration, antagonizes mescaline-induced scratching in mice.| Katalog # | CAS Nummer | Summenformel | Menge |
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| sc-204164 | 154130-99-1 | C18H22N2O•C2H2O4 | 10 mg/50 mg |
- 4-PPBP maleate
σ ligand and selective non-competitive antagonist at recombinant NR1a/2B NMDA receptors expressed in Xenopus oocytes.| Katalog # | CAS Nummer | Summenformel | Menge |
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| sc-203780 | 207572-62-1 | C21H27N ·C4H4O4 | 10 mg/50 mg |
- (+/-)-PPCC oxalate
(±)-PPCC oxalate is a selective sigma (σ) receptor ligand which is noted to exhibit high affinity for σ1 and also binds at σ2 sites| Katalog # | CAS Nummer | Summenformel | Menge |
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| sc-358806 | 932736-90-8 | C24H29NO3•C2H2O4 | 10 mg/50 mg |
- PRE-084 Hydrochloride
High affinity, selective σ1 agonist. Selective over PCP receptors and several other receptor systems. Produces antiamnesic and antitussive effects in vivo.| Katalog # | CAS Nummer | Summenformel | Menge |
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| sc-203447 | 138847-85-5 | C19H27NO3··HCl | 10 mg/50 mg |
- Rimcazole dihydrochloride
Binds to the dopamine transporter (IC50 = 57.6 nM) and inhibits dopamine uptake. Antagonist at σ receptors (IC50 values are 1480 and 386 nM at σ1 and σ2 receptors respectively). Reduces the stimulatory effects of cocaine in vivo.| Katalog # | CAS Nummer | Summenformel | Menge |
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| sc-204236 | 75859-03-9 | C21H27N3•2HCl•H2O | 10 mg/50 mg |
- (+)-SK&F 10047 hydrochloride
Prototypical σ1 receptor agonist. Behaviorally active in animal models of memory and stress.| Katalog # | CAS Nummer | Summenformel | Menge |
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| sc-204282 | 133005-41-1 | C17H23NO•HCl•xH2O | 10 mg/50 mg |
- TC 1
High affinity σ1 receptor ligand that displays selectivity over σ2 receptors (Ki values are 10 and 370 nM respectively). Exhibits low affinity for dopamine (DAT), serotonin (SERT) and noradrenalin (NET) transporters (Ki > 10 μM). Low affinity for dopamine D2 receptors (Ki = 1226 nM). Attenuates cocaine-induced locomotor activity in mice.
| Katalog # | CAS Nummer | Summenformel | Menge |
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| sc-204323 | n.n. | C19H20FNO | 10 mg/50 mg |
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