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Cancer
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ALX-260-014 Revised 19-Aug-08
Calpeptin
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SYNONYMS Z-Leu-norleucinal
PRODUCT LINE Signal Transduction
PRODUCT CATEGORY Calpains / Related Products
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Product Numbers: Format: Size: Unit Price: Quantity: Add To Cart
ALX-260-014-M005   5 mg 85.00 USD Add To Cart
ALX-260-014-M010   10 mg 160.00 USD Add To Cart
Product Specification
FORMULA: C20H30N2O4
MW: 362.5
CAS NUMBER: 117591-20-5
PURITY: ≥94% (HPLC)
APPEARANCE: White to off-white powder.
SOLUBILITY: 5mg/ml soluble in DMSO or dimethyl formamide.
SHIPPING: AMBIENT
LONG TERM STORAGE: -20°C
USE/STABILITY: Stock solutions are stable for up to 2 months when stored at -20°C.
HANDLING: Packaged under inert gas. After reconstitution, prepare aliquots and store at -20°C. Protect from light and moisture.

Product Description
Membrane permeable inhibitor of calpain I and II and cathepsin L. Promotes neurite elongation in differentiating PC12 cells. Prevents Ca2+-ionophore induced degradation of actin binding protein and P235 in platelets. Inhibits myosin light chain phosphorylation in platelets stimulated by collagen, ionomycin (Prod. No. ALX-450-006) or thrombin.
Product Specific Literature References
Inhibitory effect of di- and tripeptidyl aldehydes on calpains and cathepsins: T. Sasaki, et al.; J. Enz. Inhib. 3, 195 (1990) Abstract
Cell-penetrating inhibitors of calpain: S. Mehdi; TIBS 16, 150 (1991) Abstract
Specificity of calcium-activated neutral proteinase (CANP) inhibitors for human mu CANP and mCANP: K. Saito and R.A. Nixon; Neurochem. Res. 18, 231 (1993) Abstract
Calpeptin, a calpain inhibitor, promotes neurite elongation in differentiating PC12 cells: M. Pinter, et al.; Neurosci. Lett. 170, 91 (1994) Abstract
Further Categories Containing This Product:
Cathepsin Inhibitors
 
 
ALX-260-017 Revised 07-Jul-08
CA-074
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SYNONYMS N-[L-3-trans-Propylcarbamoyloxirane-2-carbonyl]-Ile-Pro-OH
PRODUCT LINE Cancer
PRODUCT CATEGORY Cathepsin Inhibitors
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ALX-260-017-M001   1 mg 210.00 USD Add To Cart
Product Specification
FORMULA: C18H29N3O6
MW: 383.5
CAS NUMBER: 134448-10-5
PURITY: ≥98% (HPLC)
APPEARANCE: White to off-white powder.
SOLUBILITY: Soluble in ethyl acetate (50mg/ml).
SHIPPING: AMBIENT
LONG TERM STORAGE: -20°C

Product Description
Potent and specific inhibitor of cathepsin B in vitro and in vivo.
Product Specific Literature References
Novel epoxysuccinyl peptides. Selective inhibitors of cathepsin B, in vitro: M. Murata, et al.; FEBS Lett. 280, 307 (1991) Abstract
Novel epoxysuccinyl peptides. A selective inhibitor of cathepsin B, in vivo: T. Towatari, et al.; FEBS Lett. 280, 311 (1991) Abstract
Specific assay method for the activities of cathepsin L-type cysteine proteinases: T. Inubushi, et al.; J. Biochem. 116, 282 (1994) Abstract
 
 
ALX-260-037 Revised 30-May-07
Calpain Inhibitor I
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SYNONYMS Ac-LL-Norleucinal
Ac-Leu-Leu-Nle-CHO
PRODUCT LINE Signal Transduction
PRODUCT CATEGORY Calpains / Related Products
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ALX-260-037-M010   10 mg 80.00 USD Add To Cart
ALX-260-037-M050   50 mg 310.00 USD Add To Cart
Product Specification
FORMULA: C20H37N3O4
MW: 383.5
CAS NUMBER: 110044-82-1
SOURCE/HOST: Synthetic.
PURITY: ≥96% (HPLC)
APPEARANCE: White to off-white powder.
SOLUBILITY: Soluble in DMSO, 100% ethanol or methanol.
SHIPPING: AMBIENT
LONG TERM STORAGE: +4°C
HANDLING: Protect from light and moisture.
Product Description
Inhibits calpain I (Ki=190nM), calpain II (Ki=220nM), cathepsin B (Ki=150nM) and cathepsin L (Ki=0.5nM). Inhibits neutral cysteine proteases and the proteasome. Protects against neuronal damage caused by hypoxia and ischemia. Inhibits apoptosis in thymocytes and metamyelocytes. Inhibits cell cycle progression at the G1/S border and metaphase/anaphase in CHO cells by inhibiting cyclin B degradation. Also prevents nitric oxide production by activated macrophages by interfering with the transcription of inducible nitric oxide synthase (iNOS; NOS II). Inhibits the proteolysis of IκB-α and IκB-β by the ubiquitin-proteasome complex.
Product Specific Literature References
Serine and cysteine proteinase inhibitors prevent nitric oxide production by activated macrophages by interfering with transcription of the inducible NO synthase gene: J.M. Griscavage, et al.; BBRC 215, 721 (1995) Abstract
Further Categories Containing This Product:
Proteasome / Related ProductsCathepsin InhibitorsProteases Other Products
 
 
ALX-260-038 Revised 15-Nov-05
Calpain Inhibitor II
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SYNONYMS Ac-LLM-CHO
Ac-Leu-Leu-Met-CHO
PRODUCT LINE Signal Transduction
PRODUCT CATEGORY Calpains / Related Products
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ALX-260-038-M010   10 mg 75.00 USD Add To Cart
ALX-260-038-M050   50 mg 290.00 USD Add To Cart
Product Specification
FORMULA: C19H35N3O4S
MW: 401.6
CAS NUMBER: 110115-07-6
PURITY: ≥96%
APPEARANCE: White to off-white powder.
SOLUBILITY: Soluble in 100% ethanol, methanol or DMSO.
SHIPPING: AMBIENT
LONG TERM STORAGE: -20°C
USE/STABILITY: Stock solutions are stable for up to 3 months when stored at -20°C.
HANDLING: Protect from light and moisture.
Product Description
Inhibitor of calpain I, calpain II, cathepsin B and cathepsin L.
Further Categories Containing This Product:
Cathepsin Inhibitors
 
 
ALX-260-085 Revised 23-Jan-07
Pepstatin A (synthetic)
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SYNONYMS i-Valeryl-L-Val-L-Val-AHMHA-L-Ala-AHMHA
Iva-Val-Val-Sta-Ala-Sta
PRODUCT LINE Cancer
PRODUCT CATEGORY Cathepsin Inhibitors
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Product Numbers: Format: Size: Unit Price: Quantity: Add To Cart
ALX-260-085-M005   5 mg 35.00 USD Add To Cart
ALX-260-085-M025   25 mg 95.00 USD Add To Cart
ALX-260-085-M100   100 mg 290.00 USD Add To Cart
Product Specification
SEQUENCE: i-Valeryl-L-Val-L-Val-AHMHA-L-Ala-AHMHA
(AHMHA = (3S,4S)-4-Amino-3-hydroxy-6-methyl-heptanoic acid)
FORMULA: C34H63N5O9
MW: 685.9
CAS NUMBER: 26305-03-3
MERCK INDEX: 14: 7147
RTECS: SC6155000
SOURCE/HOST: Synthetic.
PURITY: ≥98% (HPLC)
APPEARANCE: White to off-white solid.
SOLUBILITY: Soluble in DMSO, methanol or acetic acid.
SHIPPING: AMBIENT
LONG TERM STORAGE: -20°C
USE/STABILITY: Stable for at least 2 years after receipt when stored at -20°C.
HANDLING: Protect from light.
Product Description
Inhibitor of aspartate (acid) proteases, including pepsin, cathepsin D, renin, chymosin, bacterial aspartic proteinases and HIV proteases. Efficiently inhibits Fcγ receptor induction by IFN-γ. Blocks the endocytic pathway followed by an antibody when it enters the cell at the level of early endosomal compartments, resulting in inhibition of autoantigen presentation or viral transmission.
Product Specific Literature References
Localization of pepstatin's inhibitory action during Fc-mediated antibody internalization: possible implications for antibody-mediated viral transmission: I. Athanassakis, et al.; Cell. Immunol. 199, 81 (2000) Abstract
Pepstatin, a new pepsin inhibitor produced by Actinomycetes: H. Umezawa, et al.; J. Antibiot. 23, 259 (1970) Abstract
Further Categories Containing This Product:
Proteases Other ProductsAutophagy Other Products
 
 
ALX-260-120 Revised 12-Dec-07
Dnp-Pro-Leu-Gly-Met-Trp-Ser-Arg-OH
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PRODUCT LINE Cytoskeleton
PRODUCT CATEGORY MMP Substrates
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ALX-260-120-M005   5 mg 250.00 USD Add To Cart
Product Specification
SEQUENCE: 2,4-Dinitrophenyl-Pro-Leu-Gly-Met-Trp-Ser-Arg-OH
FORMULA: C44H61N13O13S
MW: 1012.1
PURITY: ≥95% (HPLC)
APPEARANCE: Yellow solid
SOLUBILITY: Soluble in DMSO; dilute with distilled water or buffer.
SHIPPING: AMBIENT
LONG TERM STORAGE: -20°C
HANDLING: Protect from light.
Product Description
Fluorogenic substrate for MMP-2 and MMP-9. Excitation: 280nm; emission 360nm.
Product Specific Literature References
Continuously recording fluorescent assays optimized for five human matrix metalloproteinases: S. Netzel-Arnett, et al.; Anal. Biochem. 195, 86 (1991) Abstract
 
 
ALX-260-121 Revised 08-Jul-05
Mca-Arg-Pro-Lys-Pro-Val-Glu-Nva-Trp-Arg-Lys(Dnp)-NH2
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PRODUCT LINE Cytoskeleton
PRODUCT CATEGORY MMP Substrates
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ALX-260-121-M001   1 mg 190.00 USD Add To Cart
Product Specification
MW: 1680.0
PURITY: ≥97%
APPEARANCE: Yellow solid.
SOLUBILITY: DMSO.
SHIPPING: AMBIENT
LONG TERM STORAGE: -20°C
HANDLING: Keep cool and dry. Protect from light.
Product Description
Fluorogenic substrate for MMP-3 and MMP-9.
 
 
ALX-260-122 Revised 12-Jun-03
Mca-Pro-Cha-Gly-Nva-His-Ala-Dap(Dnp)-NH2
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PRODUCT LINE Cytoskeleton
PRODUCT CATEGORY MMP Substrates
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ALX-260-122-M001   1 mg 190.00 USD Add To Cart
Product Specification
FORMULA: C51H65N13O15
MW: 1100.2
PURITY: ≥97%
APPEARANCE: Yellow solid.
SOLUBILITY: Soluble in DMSO.
SHIPPING: AMBIENT
LONG TERM STORAGE: -20°C
HANDLING: Protect from light.
Product Description
Fluorogenic substrate for MMP-13.
Product Specific Literature References
Biochemical characterization of human collagenase-3: V. Knäuper, et al.; J. Biol. Chem. 271, 1544 (1996) Abstract; Full Text
 
 
ALX-260-123 Revised 14-Dec-04
Mca-Pro-Leu-Ala-Nva-Dap(Dnp)-Ala-Arg-NH2
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PRODUCT LINE Cytoskeleton
PRODUCT CATEGORY MMP Substrates
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ALX-260-123-M001   1 mg 190.00 USD Add To Cart
Product Specification
MW: 1093.0
PURITY: ≥97%
APPEARANCE: Yellow solid.
SOLUBILITY: Soluble in DMSO.
SHIPPING: AMBIENT
LONG TERM STORAGE: -20°C
HANDLING: Keep cool and dry. Protect from light.
Product Description
Fluorogenic substrate for MMP-2.
 
 
ALX-260-125 Revised 12-Jun-03
Mca-Pro-Leu-Gly-Leu-Dap(Dnp)-Ala-Arg-NH2
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PRODUCT LINE Cytoskeleton
PRODUCT CATEGORY MMP Substrates
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ALX-260-125-M001   1 mg 190.00 USD Add To Cart
ALX-260-125-M005   5 mg 684.00 USD Add To Cart
Product Specification
FORMULA: C49H68N14O15
MW: 1093.2
PURITY: ≥97%
APPEARANCE: Yellow solid.
SOLUBILITY: DMSO.
SHIPPING: AMBIENT
LONG TERM STORAGE: -20°C
HANDLING: Keep cool and dry. Protect from light.
Product Description
Fluorogenic substrate for MMP-2 and MMP-7.
 
 
ALX-260-128 Revised 03-Apr-08
Actinonin
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SYNONYMS 3[[1-[[2-(Hydroxymethyl)-1-pyrrolidinyl]-carbonyl]-2-methylpropyl]-carbamoyl]-octanohydroxamic acid
PRODUCT LINE Natural Products / Antibiotics
PRODUCT CATEGORY Antitumor Antibiotics
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ALX-260-128-M005   5 mg 90.00 USD Add To Cart
Product Specification
FORMULA: C19H35N3O5
MW: 385.5
CAS NUMBER: 13434-13-4
SOURCE/HOST: Synthetic.
PURITY: ≥98%
APPEARANCE: White powder.
SOLUBILITY: Soluble in 100% ethanol.
SHIPPING: AMBIENT
LONG TERM STORAGE: -20°C

Product Description
Inhibitor of aminopeptidase M, leucine aminopeptidase and deformylase. Shows antitumor activity. Apoptosis inducer.
Product Specific Literature References
Production of actinonin, an inhibitor of aminopeptidase M, by actinomycetes: H. Umezawa, et al.; J. Antibiot. (Tokyo) 38, 1629 (1985) Abstract
Analgesic effect of actinonin, a new potent inhibitor of multiple enkephalin degrading enzymes: M. Hachisu, et al.; Life Sci. 41, 235 (1987) Abstract
Effects of an antibiotic protease inhibitor, actinonin on the growth within collagen gels of non-metastatic and metastatic mouse mammary tumors of the same origin: K. Sayama, et al.; Cancer Lett 94, 171 (1995) Abstract
Inhibition of alanyl aminopeptidase induces MAP-kinase p42/ERK2 in the human T cell line KARPAS-299: U. Lendeckel, et al.; BBRC 252, 5 (1998) Abstract
Antitumor activity of actinonin in vitro and in vivo: Y. Xu, et al.; Clin. Cancer Res. 4, 171 (1998) Abstract
Actinonin, a naturally occurring antibacterial agent, is a potent deformylase inhibitor: D.Z. Chen, et al.; Biochemistry 39, 1256 (2000) Abstract
Human mitochondrial peptide deformylase, a new anticancer target of actinonin-based antibiotics: M.D. Lee, et al.; J. Clin. Invest. 114, 1107 (2004) Abstract
Actinonin induces apoptosis in U937 leukemia cells: M. Grujic, et al.; Cancer Lett. 223, 211 (2005) Abstract
 
 
ALX-260-129 Revised 10-Feb-05
Z-Phe-Arg-AFC . trifluoroacetate
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SYNONYMS Z-FR-AFC . TFA
PRODUCT LINE Cancer
PRODUCT CATEGORY Cathepsin Substrates
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