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Adrenergics & Adrenergic Receptors / Related Products
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Items 16 of 16
ALX-350-092 Revised 03-Apr-08
Emetine . dihydrochloride
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SYNONYMS 6’,7’,10,11-Tetramethoxyemetan . 2HCl
PRODUCT LINE Natural Products / Antibiotics
PRODUCT CATEGORY Natural Products - DNA Replication Inhibitors
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ALX-350-092-M050   50 mg 10.00 USD Add To Cart
Product Specification
FORMULA: C29H40N2O4 . 2HCl
MW: 480.7 . 73.0
CAS NUMBER: 316-42-7
MERCK INDEX: 14: 3559
SOURCE/HOST: Isolated from ground roots of Uragoga ipecacuanha.
PURITY: ≥98%
APPEARANCE: White to off-white solid.
SOLUBILITY: Soluble in water or 100% ethanol.
SHIPPING: AMBIENT
LONG TERM STORAGE: +4°C
HANDLING: Protect from light. Hygroscopic.
HAZARD: TOXIC.

Product Description
Irreversibly blocks protein synthesis by inhibiting the movement of ribosome along the mRNA. Induces hypotension by blocking adrenoreceptors. Inhibits DNA replication in the early S phase. Inhibits HIF-1 activation by hypoxia. Induces apoptosis in leukemia cells. Antiamebic.
Product Specific Literature References
Inhibitors of protein biosynthesis. V. Effects of emetine on protein and nucleic acid biosynthesis in HeLa cells: A.P. Grollman; J. Biol. Chem. 243, 4089 (1968) Abstract
Cytometric analysis of DNA replication inhibited by emetine and cyclosporin A:: A: T. Schweighoffer, et al.; Histochemistry 96, 93 (1991) Abstract
Emetine allows identification of origins of mammalian DNA replication by imbalanced DNA synthesis, not through conservative nucleosome segregation: W.C. Burhans, et al.; EMBO J. 10, 4351 (1991) Abstract
Role of newly synthesized MHC class II molecules in antigen-specific antigen presentation by B cells: T. Kokuho, et al.; Immunobiology 193, 42 (1995) Abstract
Terpenoid tetrahydroisoquinoline alkaloids emetine, klugine, and isocephaeline inhibit the activation of hypoxia-inducible factor-1 in breast tumor cells: Y.D. Zhou, et al.; J. Nat. Prod. 68, 947 (2005) Abstract
The alkaloid emetine as a promising agent for the induction and enhancement of drug-induced apoptosis in leukemia cells: M. Moller, et al.; Oncol. Rep. 18, 737 (2007) Abstract
Characteristics of apoptosis induction by the alkaloid emetine in human tumour cell lines: M. Moller & M. Wink; Planta Med. 73, 1389 (2007) Abstract
 
 
ALX-350-104 Revised 10-May-07
Aaptamine
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SYNONYMS 8,9-Dimethoxy-1H-benzo[de][1,6]naphtyridine
PRODUCT LINE Natural Products / Antibiotics
PRODUCT CATEGORY Other Toxins
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ALX-350-104-M001   1 mg 90.00 USD Add To Cart
Product Specification
FORMULA: C13H12N2O2
MW: 228.3
CAS NUMBER: 85547-22-4
SOURCE/HOST: Isolated from the sponge Aaptos aaptos.
PURITY: ≥97%
APPEARANCE: Oil.
SOLUBILITY: Soluble in DMSO or 100% ethanol.
SHIPPING: AMBIENT
LONG TERM STORAGE: -20°C
HANDLING: Protect from light.
HAZARD: TOXIC.

Product Description
Competitive antagonist of α-adrenoceptors in vascular smooth muscle cells. Inhibits cancer cell growth.
Product Specific Literature References
Alpha-adrenoceptor blocking action of aaptamine, a novel marine natural product, in vascular smooth muscle: Y. Ohizumi, et al.; J. Pharm. Pharmacol. 36, 785 (1984) Abstract
Antineoplastic agents 491. Synthetic conversion of aaptamine to isoaaptamine, 9-demethylaaptamine, and 4-methylaaptamine: G.R. Pettit, et al.; J. Org. Chem. 69, 2251 (2004) Abstract
Aaptamine, a spongean alkaloid, activates p21 promoter in a p53-independent manner: S. Aoki, et al.; BBRC 342, 101 (2006) Abstract
 
 
ALX-350-111 Revised 04-Mar-05
Sibutramine . hydrochloride . monohydrate
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SYNONYMS 1-(4-Chlorophenyl-N,N-dimethyl-α-(2-methylpropyl)cyclobutanemethanamine . HCl . H2O
PRODUCT LINE Neurobiology
PRODUCT CATEGORY Adrenergics & Adrenergic Receptors / Related Products
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ALX-350-111-M250   250 mg 25.00 USD Add To Cart
ALX-350-111-G001   1 g 60.00 USD Add To Cart
Product Specification
FORMULA: C17H26ClN . HCl . H2O
MW: 279.9 . 36.5 . 18.0
CAS NUMBER: 125494-59-9
MERCK INDEX: 14: 8485
PURITY: ≥98%
APPEARANCE: White to off-white crystalline powder.
SOLUBILITY: Soluble in methanol or water (2.9mg/ml at pH 5.2).
SHIPPING: AMBIENT
LONG TERM STORAGE: +4°C
MELTINGPOINT: 193-198°C

Product Description
Anti-obesity agent. Prevents resorption of the messenger substances serotonin and noradrenalin in the brain, allowing them to act at higher concentration on nerve cells and increasing the feeling of satiety.
 
 
ALX-550-076 Revised 29-Apr-08
L-Norepinephrine . bitartrate . monohydrate
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SYNONYMS L-4-(2-Amino-1-hydroxyethyl)-1,2-benzenediol . C4H6O6 . H2O
L-Noradrenaline . C4H6O6 . H2O
PRODUCT LINE Neurobiology
PRODUCT CATEGORY Adrenergics & Adrenergic Receptors / Related Products
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ALX-550-076-G001   1 g 60.00 USD Add To Cart
Product Specification
FORMULA: C8H11NO3 . C4H6O6 . H2O
MW: 169.2 . 150.1 . 18.0
CAS NUMBER: 69815-49-2
MERCK INDEX: 14: 6695
PURITY: ≥98% (Assay)
APPEARANCE: White to off-white powder.
SOLUBILITY: Soluble in water.
SHIPPING: AMBIENT
LONG TERM STORAGE: +4°C
USE/STABILITY: Solutions may oxidize when exposed to air.
HANDLING: Protect from light.
HAZARD: VERY TOXIC.

Product Description
Adrenergic neurotransmitter.
 
 
ALX-550-077 Revised 26-Apr-07
Clenbuterol . hydrochloride
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SYNONYMS 4-Amino-3,5-dichloro-α-[[(1,1-dimethylethyl)amino]methyl]benzenemethanol . HCl
PRODUCT LINE Neurobiology
PRODUCT CATEGORY Adrenergics & Adrenergic Receptors / Related Products
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ALX-550-077-M050   50 mg 20.00 USD Add To Cart
ALX-550-077-M250   250 mg 50.00 USD Add To Cart
ALX-550-077-G001   1 g 150.00 USD Add To Cart
Product Specification
FORMULA: C12H18Cl2N2O . HCl
MW: 277.2 . 36.5
CAS NUMBER: 21898-19-1
MERCK INDEX: 14: 2347
RTECS: DN3180000
PURITY: ≥99%
APPEARANCE: White to off-white powder.
SOLUBILITY: Soluble in water, methanol or 100% ethanol.
SHIPPING: AMBIENT
LONG TERM STORAGE: +20°C
HAZARD: TOXIC.

Product Description
β2-Adrenergic receptor agonist. Bronchodilator.
Product Specific Literature References
Thiokynurenates: a new group of antagonists of the glycine modulatory site of the NMDA receptor: F. Moroni, et al.; Eur. J. Pharmacol. 199, 227 (1991) Abstract
Function and regulation of the beta 3-adrenoceptor: A.D. Strosberg & F. Pietri-Rouxel; TIPS 17, 373 (1996), (Review) Abstract
 
 
ALX-550-087 Revised 15-Sep-08
Clonidine . hydrochloride
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SYNONYMS
2-(2,6-Dichloroanilino)-2-imidazoline . hydrochloride
PRODUCT LINE Neurobiology
PRODUCT CATEGORY Adrenergics & Adrenergic Receptors / Related Products
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ALX-550-087-M050   50 mg 23.00 USD Add To Cart
Product Specification
FORMULA: C9H9Cl2N3 . HCl
MW: 230.1 . 36.5
CAS NUMBER: 4205-91-8
MERCK INDEX: 14: 2390
RTECS: NJ2490000
PURITY: ≥98% (HPLC)
APPEARANCE: White to off-white solid.
SOLUBILITY: Soluble in water (50mg/ml) or methanol.
SHIPPING: AMBIENT
LONG TERM STORAGE: +4°C
HAZARD: VERY TOXIC.

Product Description
α2-Adrenergic receptor agonist. Antihypertensive.
Further Categories Containing This Product:
Imidazoline Binding Site Ligands
 
 
ALX-550-097 Revised 04-Mar-05
Spiroxatrine
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SYNONYMS (±)-8-[(2,3-Dihydro-1,4-benzodioxin-2-yl)methyl]-1-phenyl-1,3,8-triazaspiro[4,5]-decane-4-one
PRODUCT LINE Neurobiology
PRODUCT CATEGORY Serotonergics & Serotonin Receptors / Related Products
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ALX-550-097-M005   5 mg 70.00 USD Add To Cart
Product Specification
FORMULA: C22H25N3O3
MW: 379.5
CAS NUMBER: 1054-88-2
PURITY: ≥98%
APPEARANCE: Off-white powder.
SOLUBILITY: Slightly soluble in DMSO or dimethyl formamide.
SHIPPING: AMBIENT
LONG TERM STORAGE: +4°C

Product Description
Neuroleptic agent for receptor binding studies.
Product Specific Literature References
Spiroxamide (R 5188) : A new compound producing morphine-like and chlorpromazine-like effects in animals: C.J.E. Niemegeers, et al.; Int. J. Neuropharmacol. 2, 349 (1964)
Spiroxatrine: a selective serotonin1A receptor antagonist: D.L. Nelson & E.W. Taylor; Eur. J. Pharmacol. 124, 207 (1986) Abstract
Further Categories Containing This Product:
Adrenergics & Adrenergic Receptors / Related Products
 
 
ALX-550-144 Revised 09-Dec-04
Buspirone . hydrochloride
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SYNONYMS 8-[4-[4-(2-Pyrimidinyl)-1-piperazinyl]butyl]-8-azaspiro[4,5]decane-7,9-dione . HCl
PRODUCT LINE Neurobiology
PRODUCT CATEGORY Serotonergics & Serotonin Receptors / Related Products
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ALX-550-144-G001   1 g 48.00 USD Add To Cart
Product Specification
FORMULA: C21H31N5O2 . HCl
MW: 385.5 . 36.5
CAS NUMBER: 33386-08-2
MERCK INDEX: 14: 1504
PURITY: ≥96%
APPEARANCE: White solid.
SOLUBILITY: Soluble in water.
SHIPPING: AMBIENT
LONG TERM STORAGE: +4°C
HAZARD: TOXIC.

Product Description
5-HT1A serotonin receptor agonist.
Product Specific Literature References
The discovery and development of buspirone: a new approach to the treatment of anxiety: J.S. New; Med. Res. Rev. 10, 283 (1990), (Review) Abstract
 
 
ALX-550-274 Revised 03-Mar-05
(±)-Niguldipine . hydrochloride
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SYNONYMS (±)-1,4-Dihydro-2,6-dimethyl-4-(3'-nitrophenyl)-3,5-pyridinedicarboxylic acid 3-(4',4'-diphenyl-1'-piperidinyl)propylmethyl ester . HCl
PRODUCT LINE Signal Transduction
PRODUCT CATEGORY Ca2+ Channels (L-type)
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ALX-550-274-M005   5 mg 35.00 USD Add To Cart
ALX-550-274-M025   25 mg 110.00 USD Add To Cart
Product Specification
FORMULA: C36H39N3O6 . HCl
MW: 609.7 . 36.5
CAS NUMBER: 113317-61-6
PURITY: ≥95%
APPEARANCE: Off-white to yellow solid.
SOLUBILITY: Soluble in DMSO or acetone.
SHIPPING: AMBIENT
LONG TERM STORAGE: -20°C
HANDLING: Protect from light. Adsorbs strongly to plastic.

Product Description
Extremely potent (picomolar range) inhibitor of α1A-adrenergic receptors and L-type Ca2+ channels.
Product Specific Literature References
Stereoselective binding of niguldipine enantiomers to alpha 1A- adrenoceptors labeled with [3H]5-methyl-urapidil: I. Graziadei, et al.; Eur. J. Pharmacol. 172, 329 (1989) Abstract
Niguldipine discriminates between alpha 1-adrenoceptor-mediated second messenger responses in rat cerebral cortex slices: J.P. Robinson & D.A. Kendall; Br. J. Pharmacol. 100, 3 (1990) Abstract
Further Categories Containing This Product:
Adrenergics & Adrenergic Receptors / Related Products
 
 
ALX-550-276 Revised 03-Mar-05
S-(+)-Niguldipine . hydrochloride
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SYNONYMS S-(+)-1,4-Dihydro-2,6-dimethyl-4-(3'-nitrophenyl)-3,5-pyridinedicarboxylic acid 3-(4',4'-diphenyl-1'-piperidinyl)propylmethyl ester . HCl
PRODUCT LINE Signal Transduction
PRODUCT CATEGORY Ca2+ Channels (L-type)
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ALX-550-276-M005   5 mg 160.00 USD Add To Cart
Product Specification
FORMULA: C36H39N3O6 . HCl
MW: 609.7 . 36.5
CAS NUMBER: 113165-32-5
APPEARANCE: Yellow solid.
SOLUBILITY: Soluble in DMSO or methanol.
SHIPPING: AMBIENT
LONG TERM STORAGE: -20°C
HANDLING: Protect from light. Adsorbs strongly to plastic.

Product Description
Extremely potent (picomolar range) inhibitor of α1A-adrenergic receptors and L-type Ca2+ channels.
Product Specific Literature References
(+)-Niguldipine binds with very high affinity to Ca2+ channels and to a subtype of alpha 1-adrenoceptors: R. Boer, et al.; Eur. J. Pharmacol. 172, 131 (1989) Abstract
Stereoselective binding of niguldipine enantiomers to alpha 1A- adrenoceptors labeled with [3H]5-methyl-urapidil: I. Graziadei, et al.; Eur. J. Pharmacol. 172, 329 (1989) Abstract
Pharmacological modulation of calcium and potassium channels in isolated vascular smooth muscle cells: U. Klockner, et al.; Arzneimittelforschung 39, 120 (1989) Abstract
Niguldipine discriminates between alpha 1-adrenoceptor-mediated second messenger responses in rat cerebral cortex slices: J.P. Robinson & D.A. Kendall; Br. J. Pharmacol. 100, 3 (1990) Abstract
Further Categories Containing This Product:
Adrenergics & Adrenergic Receptors / Related Products
 
 
ALX-550-306 Revised 09-Nov-07
(±)-Verapamil . hydrochloride
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SYNONYMS 5-[(3,4-Dimethoxyphenylethyl)methylamino]-2-(3,4-dimethoxyphenyl)-2-isopropyl-valeronitrile . HCl
PRODUCT LINE Signal Transduction
PRODUCT CATEGORY Ca2+ Channels (L-type)
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ALX-550-306-G001   1 g 24.00 USD