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Tyrosine Kinase Inhibitors
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ALX-151-026 Revised 20-Jun-08
N-Acetyl-Asp-Tyr(2-malonyl)-Val-Pro-Met-Leu-NH2
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PRODUCT LINE Signal Transduction
PRODUCT CATEGORY Tyrosine Kinase Inhibitors
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Product Numbers: Format: Size: Unit Price: Quantity: Add To Cart
ALX-151-026-M001   1 mg 90.00 USD Add To Cart
Product Specification
FORMULA: C39H57N7O14S
MW: 880.0
PURITY: ≥96% (HPLC)
APPEARANCE: White to off-white powder.
SOLUBILITY: Soluble in water (1mg/ml).
SHIPPING: AMBIENT
LONG TERM STORAGE: -20°C
USE/STABILITY: Peptide is very unstable.
Product Description
Peptide containing a phosphotyrosyl mimetic. Effective protein tyrosine kinase inhibitor. Inhibits the phosphoinositide 3-kinase (PI(3)K) C-terminal p85 SH2 domain.
Product Specific Literature References
L-O-(2-malonyl)tyrosine: a new phosphotyrosyl mimetic for the preparation of Src homology 2 domain inhibitory peptides: B. Ye, et al.; J. Med. Chem. 38, 4270 (1995) Abstract
Further Categories Containing This Product:
PeptidesPhosphoinositide 3-kinase [PI(3)K] / Related Products
 
 
ALX-151-027 Revised 17-Jan-05
N-Acetyl-Asp-Tyr(PO3H2)-Val-Pro-Met-Leu-NH2
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PRODUCT LINE Signal Transduction
PRODUCT CATEGORY Tyrosine Kinase Inhibitors
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ALX-151-027-M001   1 mg 90.00 USD Add To Cart
Product Specification
FORMULA: C36H57N7O13SP
MW: 858.9
PURITY: ≥96%
SOLUBILITY: Soluble in water.
SHIPPING: AMBIENT
LONG TERM STORAGE: -20°C
Product Description
Phosphotyrosine containing peptide. Effective protein tyrosine kinase inhibitor. Inhibits the phosphoinositide 3-kinase (PI(3)K) C-terminal p85 SH2 domain.
Product Specific Literature References
L-O-(2-malonyl)tyrosine: a new phosphotyrosyl mimetic for the preparation of Src homology 2 domain inhibitory peptides: B. Ye, et al.; J. Med. Chem. 38, 4270 (1995) Abstract
Further Categories Containing This Product:
PeptidesPhosphoinositide 3-kinase [PI(3)K] / Related Products
 
 
ALX-165-004 Revised 07-Feb-05
pp60v-src (137-157)
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SYNONYMS Peptide A
PRODUCT LINE Signal Transduction
PRODUCT CATEGORY Src Family Kinases / Related Products
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ALX-165-004-MC01   0.1 mg 40.00 USD Add To Cart
ALX-165-004-M001   1 mg 160.00 USD Add To Cart
Product Specification
SEQUENCE: H-Val-Ala-Pro-Ser-Asp-Ser-Ile-Gln-Ala-Glu-Glu-Trp-Tyr-Phe-Gly-Lys-Ile-Thr-Arg-Arg-Glu-OH
FORMULA: C111H168N30O35
MW: 2482.7
PURITY: ≥98%
APPEARANCE: White lyophilized powder.
SHIPPING: AMBIENT
LONG TERM STORAGE: -20°C
Product Description
Inhibitor of Src and EGF receptor tyrosine kinases. The peptide sequence corresponds to residues 137-157 of the noncatalytic domain of the transforming protein of Rous sarcoma virus (pp60v-scr).
Product Specific Literature References
A synthetic peptide corresponding to residues 137 to 157 of p60v-src inhibits tyrosine-specific protein kinases: K. Sato, et al.; BBRC 171, 1152 (1990) Abstract
Evidence for autoinhibitory regulation of the c-src gene product. A possible interaction between the src homology 2 domain and autophosphorylation site: Y. Fukami, et al.; J. Biol. Chem. 268, 1132 (1993) Abstract; Full Text
Further Categories Containing This Product:
PeptidesTyrosine Kinase Inhibitors
 
 
ALX-165-022 Revised 04-Mar-05
pp60c-src (521-533) (phosphorylated)
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PRODUCT LINE Signal Transduction
PRODUCT CATEGORY Src Family Kinases / Related Products
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ALX-165-022-MC05   0.5 mg 50.00 USD Add To Cart
ALX-165-022-M001   1 mg 80.00 USD Add To Cart
ALX-165-022-M005   5 mg 320.00 USD Add To Cart
Product Specification
SEQUENCE: H-Thr-Ser-Thr-Glu-Pro-Gln-Tyr(PO3H2)-Gln-Pro-Gly-Glu-Asn-Leu-OH
FORMULA: C62H95N16O28P
MW: 1543.5
PURITY: ≥98%
APPEARANCE: White lyophilized powder.
SHIPPING: AMBIENT
LONG TERM STORAGE: -20°C
Product Description
This peptide is derived from the C-terminal region of the c-Src protooncogene pp60c-src and binds intramolecularly or intermolecularly to the SH2 domain of the same protein.
Product Specific Literature References
Oncogenes and signal transduction [published erratum appears in Cell 1991 May 31;65(5):following 914]: L.C. Cantley, et al.; Cell 64, 281 (1991), (Review) Abstract
Selective binding of activated pp60c-src by an immobilized synthetic phosphopeptide modeled on the carboxyl terminus of pp60c-src: R.R. Roussel, et al.; PNAS 88, 10696 (1991) Abstract
Further Categories Containing This Product:
PeptidesTyrosine Kinase Inhibitors
 
 
ALX-168-003 Revised 02-Apr-03
Tyrosine Phosphorylation Site Inhibitor
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PRODUCT LINE Signal Transduction
PRODUCT CATEGORY Tyrosine Kinase Inhibitors
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ALX-168-003-M001   1 mg 60.00 USD Add To Cart
ALX-168-003-M005   5 mg 240.00 USD Add To Cart
Product Specification
SEQUENCE: H-Gly-Ser-Phe-Leu-Val-Arg-Glu-Ser-OH
FORMULA: C39H63N11O13
MW: 894.0
PURITY: ≥97%
APPEARANCE: White lyophilized powder.
SOLUBILITY: Soluble in water.
SHIPPING: AMBIENT
LONG TERM STORAGE: -20°C
Product Description
Inhibitor of EGF receptor binding to SH2. The peptide corresponds to a highly conserved amino acid sequence common in a variety of SH2-containing proteins. It is the minimum essential sequence for recognition of the phosphotyrosine site.
Product Specific Literature References
Highly conserved eight amino acid sequence in SH2 is important for recognition of phosphotyrosine site: M. Hidaka, et al.; BBRC 180, 1490 (1991) Abstract
Further Categories Containing This Product:
PeptidesSH2 & SH3 Domains
 
 
ALX-270-035 Revised 07-Dec-04
Tyrphostin AG 1295
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SYNONYMS 6,7-Dimethyl-2-phenylquinoxaline
PRODUCT LINE Signal Transduction
PRODUCT CATEGORY Tyrphostins
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ALX-270-035-M001   1 mg 30.00 USD Add To Cart
ALX-270-035-M005   5 mg 80.00 USD Add To Cart
Product Specification
FORMULA: C16H14N2
MW: 234.3
CAS NUMBER: 71897-07-9
PURITY: ≥98%
APPEARANCE: Tan solid.
SOLUBILITY: Soluble in DMSO.
SHIPPING: AMBIENT
LONG TERM STORAGE: -20°C
HANDLING: Store tightly sealed in the dark. Protect from light.

Further Categories Containing This Product:
Tyrosine Kinase InhibitorsEGFR Kinase Inhibitors
 
 
ALX-270-066 Revised 07-Apr-08
Lavendustin C
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SYNONYMS Compound 5
5-(N-2,5-Dihydroxybenzyl)aminosalicylic acid
PRODUCT LINE Natural Products / Antibiotics
PRODUCT CATEGORY Natural Products - Protein Kinase Inhibitors
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ALX-270-066-M001   1 mg 35.00 USD Add To Cart
Product Specification
FORMULA: C14H13NO5
MW: 275.3
SOURCE/HOST: Synthetic.
PURITY: ≥97%
APPEARANCE: Off-white solid.
SOLUBILITY: Soluble in DMSO or 100% ethanol.
SHIPPING: AMBIENT
LONG TERM STORAGE: -20°C
HANDLING: Protect from light.
HAZARD: TOXIC.

Product Description
Potent inhibitor of protein tyrosine kinases and Ca2+/calmodulin-dependent kinase II. Acts also as an inhibitor of EGFR tyrosine kinase and pp60c-src kinase.
Product Specific Literature References
Isolation of a novel tyrosine kinase inhibitor, lavendustin A, from Streptomyces griseolavendus: T. Onoda, et al.; J. Nat. Prod. 52, 1252 (1989) Abstract
Long-term potentiation in the hippocampus is blocked by tyrosine kinase inhibitors: T.J. O'Dell, et al.; Nature 353, 558 (1991) Abstract
Hypericin and pseudohypericin specifically inhibit protein kinase C: possible relation to their antiretroviral activity: I. Takahashi, et al.; BBRC 165, 1207 (1989) Abstract
Inhibition of crystal-induced neutrophil activation by a protein tyrosine kinase inhibitor: H.M. Burt, et al.; J. Leukoc. Biol. 55, 112 (1994) Abstract
Endotoxin increases intercellular resistance in microvascular endothelial cells by a tyrosine kinase pathway: D. Lidington, et al.; J. Cell Physiol. 185, 117 (2000) Abstract
 
 
ALX-270-088 Revised 07-Apr-05
ML-7 . hydrochloride
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SYNONYMS 1-(5-Iodonaphthalene-1-sulfonyl)-1H-hexahydro-1,4-diazepine . HCl
PRODUCT LINE Signal Transduction
PRODUCT CATEGORY Tyrosine Kinase Inhibitors
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ALX-270-088-M005   5 mg 40.00 USD Add To Cart
ALX-270-088-M025   25 mg 160.00 USD Add To Cart
Product Specification
FORMULA: C15H17IN2O2S . HCl
MW: 416.0 . 36.5
CAS NUMBER: 110448-33-4
PURITY: ≥98%
APPEARANCE: White to off-white solid.
SOLUBILITY: Soluble in DMSO (can be further diluted with water), 100% ethanol (warm) or methanol.
SHIPPING: AMBIENT
LONG TERM STORAGE: -20°C
HANDLING: Protect from light.

Product Description
Inhibits smooth-muscle myosin light chain kinase, protein kinase C (PKC), and cAMP-dependent protein kinase (PKA).
Product Specific Literature References
Selective inhibition of catalytic activity of smooth muscle myosin light chain kinase: M. Saitoh, et al.; J. Biol. Chem. 262, 7796 (1987) Abstract; Full Text
Further Categories Containing This Product:
PKC InhibitorsPKA InhibitorsMyosin Light Chain Kinase Inhibitors
 
 
ALX-270-098 Revised 16-Nov-06
Erbstatin analog
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SYNONYMS Methyl 2,5-dihydroxycinnamate
PRODUCT LINE Signal Transduction
PRODUCT CATEGORY EGFR Kinase Inhibitors
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ALX-270-098-M005   5 mg 55.00 USD Add To Cart
Product Specification
FORMULA: C10H10O4
MW: 194.2
CAS NUMBER: 63177-57-1
PURITY: ≥98% (HPLC)
APPEARANCE: Off-white to light brown crystalline solid.
SOLUBILITY: Soluble in methanol, DMSO or dilute aqueous base.
SHIPPING: AMBIENT
LONG TERM STORAGE: +4°C
HANDLING: Protect from light.
HAZARD: TOXIC.

Product Description
Inhibitor of epidermal growth factor receptor (EGFR) tyrosine kinase. Considerably longer half-life in aqueous solution than erbstatin itself. Induces apoptosis.
Product Specific Literature References
Inhibition of epidermal growth factor-induced DNA synthesis by tyrosine kinase inhibitors: K. Umezawa, et al.; FEBS Lett. 260, 198 (1990) Abstract
Inhibition of epidermal growth factor receptor functions by tyrosine kinase inhibitors in NIH3T3 cells: K. Umezawa, et al.; FEBS Lett. 314, 289 (1992) Abstract
Induction of mouse thymocyte apoptosis by inhibitors of tyrosine kinases is associated with dephosphorylation of nuclear proteins: Y. Azuma, et al.; Cell Immunol. 152, 271 (1993) Abstract
Inhibition of Abelson oncogene function by erbstatin analogues: M. Kawada, et al.; Drugs Exp. Clin. Res. 19, 235 (1993) Abstract
Further Categories Containing This Product:
Tyrosine Kinase InhibitorsApoptosis Inducers & Inhibitors Other Products
 
 
ALX-270-129 Revised 18-Jan-08
Tyrphostin AG 18
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SYNONYMS Tyrphostin A23
Tyrphostin RG 50858
Tyrphostin RG 50810
(3,4-Dihydroxybenzylidene)malononitrile
α-Cyano-(3,4-dihydroxy)cinnamonitrile
PRODUCT LINE Signal Transduction
PRODUCT CATEGORY Tyrphostins
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ALX-270-129-M005   5 mg 35.00 USD Add To Cart
ALX-270-129-M025   25 mg 100.00 USD Add To Cart
Product Specification
FORMULA: C10H6N2O2
MW: 186.2
CAS NUMBER: 118409-57-7
PURITY: ≥98%
APPEARANCE: White solid.
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 I: synthesis and biological activity of protein tyrosine kinase inhibitors: A. Gazit, et al.; J. Med. Chem. 32, 2344 (1989) Abstract
Tyrphostins inhibit epidermal growth factor (EGF)-receptor tyrosine kinase activity in living cells and EGF-stimulated cell proliferation: R.M. Lyall, et al.; J. Biol. Chem. 264, 14503 (1989) Abstract; Full Text
Cholecystokinin rapidly activates mitogen-activated protein kinase in rat pancreatic acini: R.D. Duan & J.A. Williams; Am. J. Physiol. 267, G401 (1994) Abstract
Role of tyrosine kinase and protein kinase C in the steroidogenic actions of angiotensin II, alpha-melanocyte-stimulating hormone and corticotropin in the rat adrenal cortex: S. Kapas, et al.; Biochem. J. 305, 433 (1995) Abstract
Differential activation of mitogen-activated protein kinase and S6 kinase signaling pathways by 12-O-tetradecanoylphorbol-13-acetate (TPA) and insulin. Evidence for involvement of a TPA-stimulated protein- tyrosine kinase: R. Seger, et al.; J. Biol. Chem. 270, 28325 (1995) Abstract; Full Text
Further Categories Containing This Product:
EGFR Kinase InhibitorsTyrosine Kinase Inhibitors
 
 
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
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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: