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Signal Transduction
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 Items 140-160 of 2948 Page 8 of 148 Select Page: << 1 2 3 4 5 6 7 8 9 10  >>  
ALX-270-139 Revised 25-Nov-04
Tyrphostin AG 370
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SYNONYMS Tyrphostin B7
2-Amino-4-(1H-indol-5-yl)-1,1,3-tricyanobuta-1,3-diene
PRODUCT LINE Signal Transduction
PRODUCT CATEGORY Tyrphostins
Ordering Information
Product Numbers: Format: Size: Unit Price: Quantity: Add To Cart
ALX-270-139-M001   1 mg 50.00 USD Add To Cart
ALX-270-139-M005   5 mg 190.00 USD Add To Cart
Product Specification
FORMULA: C15H9N5
MW: 259.3
PURITY: ≥99%
APPEARANCE: Yellow solid.
SOLUBILITY: Soluble in DMSO.
SHIPPING: AMBIENT
LONG TERM STORAGE: -20°C
HANDLING: Store tightly sealed in the dark. Protect from light.

Product Specific Literature References
Inhibition of protein-tyrosine kinases by tyrphostins: A. Levitzki, et al.; Meth. Enzymol. 201, 347 (1991) Abstract
Inhibition of platelet-derived growth factor-induced mitogenesis and tyrosine kinase activity in cultured bone marrow fibroblasts by tyrphostins: M.C. Bryckaert; Exp. Cell. Res. 199, 255 (1992) Abstract
 
 
ALX-270-141 Revised 07-Dec-04
Tyrphostin AG 527
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SYNONYMS Tyrphostin B44
(-)-(R)-N-(α-Methylbenzyl)-3,4-dihydroxybenzylidenecyanoacetamide
PRODUCT LINE Signal Transduction
PRODUCT CATEGORY Tyrphostins
Ordering Information
Product Numbers: Format: Size: Unit Price: Quantity: Add To Cart
ALX-270-141-M005   5 mg 25.00 USD Add To Cart
ALX-270-141-M025   25 mg 90.00 USD Add To Cart
Product Specification
FORMULA: C18H16N2O3
MW: 308.3
CAS NUMBER: 133550-32-0
PURITY: ≥98%
SOLUBILITY: Soluble in DMSO or 100% ethanol.
SHIPPING: AMBIENT
LONG TERM STORAGE: -20°C
HANDLING: Store tightly sealed in the dark. Protect from light.

Product Specific Literature References
Tyrphostins. 2. Heterocyclic and alpha-substituted benzylidenemalononitrile tyrphostins as potent inhibitors of EGF receptor and ErbB2/neu tyrosine kinases: A. Gazit, et al.; J. Med. Chem. 34, 1896 (1991) Abstract
Further Categories Containing This Product:
EGFR Kinase InhibitorsTyrosine Kinase Inhibitors
 
 
ALX-270-142 Revised 11-Dec-04
Tyrphostin AG 555
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SYNONYMS Tyrphostin B46
N-(3-Phenylpropyl)-3,4-dihydroxy-benzylidenecyanoacetamide
α-Cyano-(3,4-dihydroxy)-N-(3-phenylpropyl)cinnamamide
PRODUCT LINE Signal Transduction
PRODUCT CATEGORY Tyrphostins
Ordering Information
Product Numbers: Format: Size: Unit Price: Quantity: Add To Cart
ALX-270-142-M005   5 mg 25.00 USD Add To Cart
ALX-270-142-M025   25 mg 90.00 USD Add To Cart
Product Specification
FORMULA: C19H18N2O3
MW: 322.4
PURITY: ≥98%
SOLUBILITY: Soluble in DMSO or ethanol.
SHIPPING: AMBIENT
LONG TERM STORAGE: -20°C
HANDLING: Store tightly sealed in the dark. Protect from light.

Product Specific Literature References
Tyrphostins. 2. Heterocyclic and alpha-substituted benzylidenemalononitrile tyrphostins as potent inhibitors of EGF receptor and ErbB2/neu tyrosine kinases: A. Gazit, et al.; J. Med. Chem. 34, 1896 (1991) Abstract
Further Categories Containing This Product:
EGFR Kinase InhibitorsTyrosine Kinase Inhibitors
 
 
ALX-270-143 Revised 20-Feb-08
Tyrphostin AG 494
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SYNONYMS Tyrphostin B48
N-Phenyl-3,4-dihydroxybenzylidenecyanoacetamide
α-Cyano-(3,4-dihydroxy)-N-phenylcinnamamide
PRODUCT LINE Signal Transduction
PRODUCT CATEGORY Tyrphostins
Ordering Information
Product Numbers: Format: Size: Unit Price: Quantity: Add To Cart
ALX-270-143-M005   5 mg 25.00 USD Add To Cart
ALX-270-143-M025   25 mg 90.00 USD Add To Cart
Product Specification
FORMULA: C16H12N2O3
MW: 280.3
CAS NUMBER: 133550-35-3
PURITY: ≥98%
APPEARANCE: Yellow solid.
SOLUBILITY: Soluble in DMSO or 100% ethanol.
SHIPPING: AMBIENT
LONG TERM STORAGE: -20°C
HANDLING: Protect from light.

Product Description
Blocks CDK2 activation and causes cells to arrest at late G1 and during S phase.
Product Specific Literature References
Tyrphostins. 2. Heterocyclic and alpha-substituted benzylidenemalononitrile tyrphostins as potent inhibitors of EGF receptor and ErbB2/neu tyrosine kinases: A. Gazit, et al.; J. Med. Chem. 34, 1896 (1991) Abstract
Tyrphostin AG 494 blocks Cdk2 activation: N. Osherov & A. Levitzki; FEBS Lett. 410, 187 (1997) Abstract
Inhibition of Cdk2 activation by selected tyrphostins causes cell cycle arrest at late G1 and S phase: N. Kleinberger-Doron, et al.; Exp. Cell Res. 241, 340 (1998) Abstract
 
 
ALX-270-144 Revised 07-Dec-04
Tyrphostin AG 835
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SYNONYMS Tyrphostin B50
(+)-(S)-N-(α-Methylbenzyl)-3,4-dihydroxybenzylidenecyanoacetamide
PRODUCT LINE Signal Transduction
PRODUCT CATEGORY Tyrphostins
Ordering Information
Product Numbers: Format: Size: Unit Price: Quantity: Add To Cart
ALX-270-144-M005   5 mg 25.00 USD Add To Cart
ALX-270-144-M025   25 mg 90.00 USD Add To Cart
Product Specification
FORMULA: C18H16N2O3
MW: 308.3
CAS NUMBER: 133550-37-5
PURITY: ≥98%
APPEARANCE: Yellow solid.
SOLUBILITY: Soluble in DMSO or 100% ethanol.
SHIPPING: AMBIENT
LONG TERM STORAGE: -20°C
HANDLING: Store tightly sealed in the dark. Protect from light.

Product Specific Literature References
Tyrphostins. 2. Heterocyclic and alpha-substituted benzylidenemalononitrile tyrphostins as potent inhibitors of EGF receptor and ErbB2/neu tyrosine kinases: A. Gazit, et al.; J. Med. Chem. 34, 1896 (1991) Abstract
Further Categories Containing This Product:
EGFR Kinase InhibitorsTyrosine Kinase Inhibitors
 
 
ALX-270-145 Revised 11-Dec-04
Tyrphostin AG 698
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SYNONYMS Tyrphostin B52
N-(2-Phenylethyl)-3,4-dihydroxybenzylidenecyanoacetamide
PRODUCT LINE Signal Transduction
PRODUCT CATEGORY Tyrphostins
Ordering Information
Product Numbers: Format: Size: Unit Price: Quantity: Add To Cart
ALX-270-145-M005   5 mg 30.00 USD Add To Cart
ALX-270-145-M025   25 mg 85.00 USD Add To Cart
Product Specification
FORMULA: C18H16N2O3
MW: 308.3
PURITY: ≥98%
SOLUBILITY: Soluble in DMSO or 100% ethanol.
SHIPPING: AMBIENT
LONG TERM STORAGE: -20°C
HANDLING: Store tightly sealed in the dark. Protect from light.

 
 
ALX-270-146 Revised 11-Dec-04
Tyrphostin AG 556
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SYNONYMS Tyrphostin B56
N-(4-Phenylbutyl)-3,4-dihydroxybenzylidenecyanoacetamide
α-Cyano-(3,4-dihydroxy)-N-(4-phenylbutyl)cinnamamide
PRODUCT LINE Signal Transduction
PRODUCT CATEGORY Tyrphostins
Ordering Information
Product Numbers: Format: Size: Unit Price: Quantity: Add To Cart
ALX-270-146-M005   5 mg 25.00 USD Add To Cart
ALX-270-146-M025   25 mg 85.00 USD Add To Cart
Product Specification
FORMULA: C20H20N2O3
MW: 336.4
CAS NUMBER: 133550-41-1
PURITY: ≥98%
APPEARANCE: Yellow solid.
SOLUBILITY: Soluble in dimethyl formamide or DMSO.
SHIPPING: AMBIENT
LONG TERM STORAGE: -20°C
HANDLING: Store tightly sealed in the dark. Protect from light.

Product Specific Literature References
Tyrphostins. 2. Heterocyclic and alpha-substituted benzylidenemalononitrile tyrphostins as potent inhibitors of EGF receptor and ErbB2/neu tyrosine kinases: A. Gazit, et al.; J. Med. Chem. 34, 1896 (1991) Abstract
Further Categories Containing This Product:
EGFR Kinase InhibitorsTyrosine Kinase Inhibitors
 
 
ALX-270-147 Revised 03-Dec-04
Tyrphostin AG 528
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SYNONYMS Tyrphostin B66
N-(3',4'-Dihydroxybenzylidenecyanoacetyl)indoline
PRODUCT LINE Signal Transduction
PRODUCT CATEGORY Tyrphostins
Ordering Information
Product Numbers: Format: Size: Unit Price: Quantity: Add To Cart
ALX-270-147-M005   5 mg 30.00 USD Add To Cart
ALX-270-147-M025   25 mg 85.00 USD Add To Cart
Product Specification
FORMULA: C18H14N2O3
MW: 306.3
PURITY: ≥98%
SOLUBILITY: Soluble in DMSO.
SHIPPING: AMBIENT
LONG TERM STORAGE: -20°C
HANDLING: Store tightly sealed in the dark. Protect from light.

 
 
ALX-270-148 Revised 09-Dec-04
Tyrphostin RG 13022
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SYNONYMS 2-(3',4'-Dimethoxyphenyl)-1-(3''-pyridinyl)acrylonitrile
α-(3'-Pyridyl)-(3,4-dimethoxy)cinnamonitrile
PRODUCT LINE Signal Transduction
PRODUCT CATEGORY Tyrphostins
Ordering Information
Product Numbers: Format: Size: Unit Price: Quantity: Add To Cart
ALX-270-148-M001   1 mg 30.00 USD Add To Cart
ALX-270-148-M005   5 mg 85.00 USD Add To Cart
Product Specification
FORMULA: C16H14N2O2
MW: 266.3
CAS NUMBER: 136831-48-6
PURITY: ≥98%
SOLUBILITY: Soluble in DMSO or 100% ethanol.
SHIPPING: AMBIENT
LONG TERM STORAGE: -20°C
HANDLING: Store tightly sealed in the dark. Protect from light.

 
 
ALX-270-149 Revised 09-Dec-04
Tyrphostin RG 14620
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SYNONYMS 2-(3',5'-Dichlorophenyl)-1-(3''-pyridinyl)acrylonitrile
α-(3'-Pyridyl)-3,5-dichloro)cinnamonitrile
PRODUCT LINE Signal Transduction
PRODUCT CATEGORY Tyrphostins
Ordering Information
Product Numbers: Format: Size: Unit Price: Quantity: Add To Cart
ALX-270-149-M001   1 mg 30.00 USD Add To Cart
ALX-270-149-M005   5 mg 85.00 USD Add To Cart
Product Specification
FORMULA: C14H8Cl2N2
MW: 275.1
CAS NUMBER: 136831-49-7
PURITY: ≥98%
APPEARANCE: White solid.
SOLUBILITY: Soluble in warm DMSO.
SHIPPING: AMBIENT
LONG TERM STORAGE: -20°C
HANDLING: Store tightly sealed in the dark. Protect from light.

 
 
ALX-270-150 Revised 05-Oct-06
Vinpocetine
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SYNONYMS Eburnamenine-14-carboxylic acid-ethyl ester
PRODUCT LINE Signal Transduction
PRODUCT CATEGORY Phosphodiesterases / Related Products
Ordering Information
Product Numbers: Format: Size: Unit Price: Quantity: Add To Cart
ALX-270-150-M005   5 mg 30.00 USD Add To Cart
ALX-270-150-M025   25 mg 70.00 USD Add To Cart
Product Specification
FORMULA: C22H26N2O2
MW: 350.5
CAS NUMBER: 42971-09-5
MERCK INDEX: 14: 9991
RTECS: JW4792000
PURITY: ≥98%
APPEARANCE: White to off-white solid.
SOLUBILITY: Soluble in DMSO, 100% ethanol or acetone.
SHIPPING: AMBIENT
LONG TERM STORAGE: +20°C
HAZARD: HARMFUL.

Product Description
Selective inhibitor of Ca2+/calmodulin-dependent phosphodiesterase 1 (PDE1).
Product Specific Literature References
Effects of vinpocetine on cyclic nucleotide metabolism in vascular smooth muscle: M. Hagiwara, et al.; Biochem. Pharmacol. 33, 453 (1984) Abstract
Effects of selective inhibitors on cyclic nucleotide phosphodiesterases of rabbit aorta: H.S. Ahn, et al.; Biochem. Pharmacol. 38, 3331 (1989) Abstract
Regulation of cyclic AMP metabolism in bovine adrenal medullary cells: P.D. Marley & K.A. Thomsom; Biochem. Pharmacol. 44, 2105 (1992) Abstract
Cyclic 3',5'-nucleotide diesterases in dynamics of cAMP and cGMP in rat collecting duct cells: M. Yamaki, et al.; Am. J. Physiol. 262, F957 (1992) Abstract
Modulation of TNF alpha and IL-1 beta from endotoxin-stimulated monocytes by selective PDE isozyme inhibitors: K. Molnar-Kimber, et al.; Agents Actions 39, C77 (1993) Abstract
 
 
ALX-270-151 Revised 10-May-05
W-5 . hydrochloride