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ALX-350-302
Revised 14-Dec-07
Imperatorin
PRODUCT LINE
Natural Products / Antibiotics
PRODUCT CATEGORY
Natural Products - Apoptosis Inducers & Inhibitors
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ALX-350-302-M002
2 mg
70.00 USD
Product Specification
FORMULA:
C
16
H
14
O
4
MW:
270.3
PURITY:
≥99% (HPLC)
APPEARANCE:
White to off-white crystalline solid.
SOLUBILITY:
Soluble in DMSO or dimethyl formamide; slightly soluble in methanol or water. Almonst insoluble in 100% ethanol.
SHIPPING:
AMBIENT
LONG TERM STORAGE:
-20°C
Product Description
The furanocoumarins heraclenin (Prod. No.
ALX-350-303
) and imperatorin (Prod. No.
ALX-350-302
) inhibit T cell-receptor-mediated proliferation in human primary T cells in a concentration-dependent manner. Both compounds also induce apoptosis. While imperatorin induces DNA fragmentation at the G1/S phase of the cell cycle, heraclenin induces DNA fragmentation at the G2/M phases of the cell cycle, thus despite a close structural similarity they induce apoptosis in mechanistically different ways. Imperatorin inhibits HIV-1 replication as well as the expression of ICAM-1 in U937 foam cells. Inhibits voltage-dependent calcium channel.
Product Specific Literature References
Expression of intercellular adhesion molecule-1 in U937 foam cells and inhibitory effect of imperatorin:
P.Y. Yang, et al.; Acta Pharmacol. Sin.
23
, 327 (2002)
Abstract
Imperatorin, a furanocoumarin from Angelica dahurica (Umbelliferae), induces cytochrome c-dependent apoptosis in human promyelocytic leukaemia, HL-60 Cells:
H.O. Pae, et al.; Pharmacol. Toxicol.
91
, 40 (2002)
Abstract
Coumarins from Opopanax chironium. New dihydrofuranocoumarins and differential induction of apoptosis by imperatorin and heraclenin:
G. Appendino, et al.; J. Nat. Prod.
67
, 532 (2004)
Abstract
Imperatorin inhibits T-cell proliferation by targeting the transcription factor NFAT:
N. Marquez, et al.; Planta Med.
70
, 1016 (2004)
Abstract
Imperatorin inhibits HIV-1 replication through an Sp1-dependent pathway:
R. Sancho, et al.; J. Biol. Chem.
279
, 37349 (2004)
Abstract
;
Full Text
Imperatorin induces vasodilatation possibly via inhibiting voltage dependent calcium channel and receptor-mediated Ca2+ influx and release:
J.Y. He, et al.; Eur. J. Pharmacol.
573
, 170 (2007)
Abstract
Related Products
ALX-350-303
Heraclenin
Further Categories Containing This Product:
DNA Fragmentation & Chromatin Condensation
•
Natural Products - Antiviral / anti-HIV Agents
•
CD11a, CD18 [LFA-1] & CD54 [ICAM-1], CD102 [ICAM-2], CD50 [ICAM-3] / Related Products
•
Ca2+ Channels Other Products
•
HIV / AIDS / Related Products
ALX-385-024
Revised 06-Oct-08
Isorhamnetin
SYNONYMS
3-Methylquercetin
3'-Methoxy-3,4',5,7-tetrahydroxyflavone
3,5,7-Trihydroxy-2-(4-hydroxy-3-methoxyphenyl)-4-benzopyrone
PRODUCT LINE
Natural Products / Antibiotics
PRODUCT CATEGORY
Flavonols
Ordering Information
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ALX-385-024-M005
5 mg
90.00 USD
ALX-385-024-M010
10 mg
150.00 USD
Product Specification
FORMULA:
C
16
H
12
O
7
MW:
316.3
CAS NUMBER:
480-19-3
PURITY:
≥98% (HPLC)
APPEARANCE:
Yellow solid.
SOLUBILITY:
Soluble in acetone, methanol, ethylacetate or DMSO. Only sparingly soluble in water.
SHIPPING:
AMBIENT
LONG TERM STORAGE:
+4°C
HAZARD:
MAY BE CARCINOGENIC. HARMFUL.
Product Description
Antiviral agent. Antioxidant. Antitumor compound. Apoptosis inducer.
Product Specific Literature References
Anti-tumor promoting activity of polyphenols from Cowania mexicana and Coleogyne ramosissima:
H. Ito, et al.; Cancer Lett.
143
, 5 (1999)
Abstract
Inhibition of xanthine oxidase by flavonoids:
A. Nagao, et al.; Biosci. Biotechnol. Biochem.
63
, 1787 (1999)
Abstract
Effects of intrinsic fluorescence and quenching on fluorescence-based screening of natural products:
L. Zou, et al.; Phytomedicine
9
, 263 (2002)
Abstract
Antioxidant effects of isorhamnetin 3,7-di-O-beta-D-glucopyranoside isolated from mustard leaf (Brassica juncea) in rats with streptozotocin-induced diabetes:
T. Yokozawa, et al.; J. Agric. Food Chem.
50
, 5490 (2002)
Abstract
Effect of five flavonoid compounds isolated from leaves of Diospyros kaki on stimulus-induced superoxide generation and tyrosyl phosphorylation of proteins in human neutrophils:
G. Chen, et al.; Clin. Chim. Acta
326
, 169 (2002)
Abstract
Isorhamnetin prevent endothelial cell injuries from oxidized LDL via activation of p38MAPK:
M. Bao & Y. Lou; Eur. J. Pharmacol.
547
, 22 (2006)
Abstract
The flavonoid component isorhamnetin in vitro inhibits proliferation and induces apoptosis in Eca-109 cells:
G. Ma, et al.; Chem. Biol. Interact.
167
, 153 (2007)
Abstract
Further Categories Containing This Product:
Natural Products - Antitumor Reagents
•
Natural Products - Apoptosis Inducers & Inhibitors
•
Natural Products - Antioxidants
•
Natural Products - Antiviral / anti-HIV Agents
ALX-350-225
Revised 29-Sep-08
Limonin
SYNONYMS
Limonoic acid di-δ-lactone
PRODUCT LINE
Natural Products / Antibiotics
PRODUCT CATEGORY
Natural Products - Chemopreventive Agents
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ALX-350-225-M050
50 mg
60.00 USD
Product Specification
FORMULA:
C
26
H
30
O
8
MW:
470.5
CAS NUMBER:
1180-71-8
MERCK INDEX:
14:
5494
SOURCE/HOST:
Isolated from grapefruit seed.
PURITY:
≥98% (HPLC)
APPEARANCE:
White to off-white solid.
SOLUBILITY:
Soluble in 100% ethanol or glacial acetic acid; slightly soluble in water.
SHIPPING:
AMBIENT
LONG TERM STORAGE:
+20°C
Product Description
Bitter principle of citrus fruits. Inhibits chemically induced carcinogenesis. Inhibits HIV-1 replication. Shows antinociceptive effect. Does not possess any inherent antioxidant activity.
Product Specific Literature References
V.P. Maier, et al.; ACS Symposium Series
143
, 63 (1980)
J.A. Klocke & I. Kubo; Ent. Exp. & Appl.
32
, 299 (1982)
R.L. Rouseff; J. Agric. Food Chem.
30
, 504 (1982)
M.A. Altieri, et al.; Protect. Ecol.
6
, 91 (1984)
The effect of citrus limonoids on hamster buccal pouch carcinogenesis:
E.G. Miller, et al.; Carcinogenesis
10
, 1535 (1989)
Abstract
L.K.T. Lam, et al.; ACS Symposium Series
546
, 209 (1994)
Antinociceptive and anti-inflammatory activities of limonin isolated from the fruits of Evodia rutaecarpa var. bodinieri:
H. Matsuda, et al.; Planta Med.
64
, 339 (1998)
Abstract
Citrus limonoids obacunone and limonin inhibit azoxymethane-induced colon carcinogenesis in rats:
T. Tanaka, et al.; Biofactors
13
, 213 (2000)
Abstract
Effect of limonin and nomilin on HIV-1 replication on infected human mononuclear cells:
L. Battinelli, et al.; Planta Med.
69
, 910 (2003)
Abstract
Evaluation of the antioxidant capacity of limonin, nomilin, and limonin glucoside:
A.P. Breksa, 3rd & G.D. Manners; J. Agric. Food Chem.
54
, 3827 (2006)
Abstract
Further Categories Containing This Product:
Natural Products - Antiviral / anti-HIV Agents
•
Natural Products for Neurological Research
•
Analgesic / Anti-nociceptive Agents / Related Products
•
Active Substances from Fruit and Vegetables
ALX-350-294
Revised 16-Jun-08
Manzamine A
PRODUCT LINE
Natural Products / Antibiotics
PRODUCT CATEGORY
Natural Products - Anti-inflammatory Agents
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ALX-350-294-M001
1 mg
195.00 USD
Product Specification
FORMULA:
C
36
H
44
N
4
O
MW:
548.8
CAS NUMBER:
104196-68-1
SOURCE/HOST:
Isolated from
Xestospongia sp
.
PURITY:
>98% (HPLC)
FORMULATION:
Yellow oil
SOLUBILITY:
Soluble in DMSO, methanol or 100% ethanol.
SHIPPING:
AMBIENT
LONG TERM STORAGE:
-20°C
Product Description
β-Carboline alkaloid with anti-inflammatory, antimalarial, antifungal, anti-HIV-1and insecticidal activity. Also active against the Gram-positive bacteria
Bacillus subtilis
and
Staphylococcus aureus
. Inhibits GSK-3. Has native fluorescence, highest when solubilized in methanol (Ex: 340nm, Em: 387nm).
Product Specific Literature References
Four new bioactive manzamine-type alkaloids from the Philippine marine sponge Xestospongia ashmorica
:
R.A. Edrada, et al.; J. Nat. Prod.
59
, 1056 (1996)
Abstract
In vivo antimalarial activity of the beta-carboline alkaloid manzamine A
:
K.K. Ang, et al.; Antimicrob. Agents Chemother.
44
, 1645 (2000)
Abstract
;
Full Text
Immune-mediated parasite clearance in mice infected with Plasmodium berghei following treatment with manzamine A
:
K.K. Ang, et al.; Parasitol. Res.
87
, 715 (2001)
Abstract
New manzamine alkaloids with activity against infectious and tropical parasitic diseases from an Indonesian sponge
:
K.V. Rao, et al.; J. Nat. Prod.
66
, 823 (2003)
Abstract
Spectrofluorimetric determination of manzamine A in spiked human urine and plasma
:
A. Khalil, et al.; Pharmazie
58
, 385 (2003)
Abstract
New manzamine alkaloids from an Indo-Pacific sponge. Pharmacokinetics, oral availability, and the significant activity of several manzamines against HIV-I, AIDS opportunistic infections, and inflammatory diseases
:
M. Yousaf, et al.; J. Med. Chem.
47
, 3512 (2004)
Abstract
Antimalarial activity of a new family of analogues of manzamine A:
J.D. Winkler, et al.; Org. Lett.
8
, 2591 (2006)
Abstract
Glycogen synthase kinase-3 (GSK-3) inhibitory activity and structure-activity relationship (SAR) studies of the manzamine alkaloids. Potential for Alzheimer’s disease:
M. Hamann, et al.; J. Nat. Prod.
70
, 1397 (2007)
Abstract
Further Categories Containing This Product:
Natural Products - Antimalarial Agents
•
Malaria / Related Products
•
Natural Products with Antibiotic Activity
•
Natural Products - Antiviral / anti-HIV Agents
•
Natural Products - Antifungal Agents
•
GSK-3 Inhibitors
•
Pesticides / Related Products
•
Alkaloids
ALX-350-274
Revised 16-Jun-08
Myriocin
SYNONYMS
ISP-1
Thermozymocidin
2S,3R,4R,6E-2-Amino-3,4-dihydroxy-2-hydroxymethyl-14-oxo-6-eicosenoic acid
PRODUCT LINE
Natural Products / Antibiotics
PRODUCT CATEGORY
Natural Products - Immunomodulators
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ALX-350-274-M005
5 mg
90.00 USD
Product Specification
FORMULA:
C
21
H
39
NO
6
MW:
401.5
CAS NUMBER:
35891-70-4
RTECS:
JX3890000
PURITY:
≥98% (TLC)
APPEARANCE:
White to off-white solid.
SOLUBILITY:
Soluble in DMSO (25mg/ml; heat briefly in boiling water bath) or in dilute base (5mg/ml; 50mM NaOH).
SHIPPING:
SHIPPED ON BLUE ICE
LONG TERM STORAGE:
-20°C
HAZARD:
HARMFUL.
Product Description
Potent immunosuppressant ~10 to 100-fold more potent than cyclosporin A (Prod. No.
ALX-380-002
). Blocks sphingolipid biosynthesis by inhibiting serine palmitoyltransferase (K
i
=0.28nM). Induces apoptosis by depletion of cellular sphingolipids. Inhibits proliferation of an IL-2-dependent mouse cytotoxic cell line CTLL-1 (IC
50
=15nM).
Product Specific Literature References
Fungal metabolites. Part 11. A potent immunosuppressive activity found in Isaria sinclairii metabolite:
T. Fujita, et al.; J. Antibiot.
47
, 208 (1994)
Abstract
Serine palmitoyltransferase is the primary target of a sphingosine-like immunosuppressant, ISP-1/myriocin:
Y. Miyake, et al.; BBRC
211
, 396 (1995)
Abstract
Ceramide and its interconvertible metabolite sphingosine function as indispensable lipid factors involved in survival and dendritic differentiation of cerebellar Purkinje cells:
S. Furuya, et al.; J. Neurochem.
71
, 366 (1998)
Abstract
Complete removal of sphingolipids from the plasma membrane disrupts cell to substratum adhesion of mouse melanoma cells
:
K. Hidari, et al.; J. Biol. Chem.
271
, 14636 (1996)
Abstract
Sli2 (Ypk1), a homologue of mammalian protein kinase SGK, is a downstream kinase in the sphingolipid-mediated signaling pathway of yeast:
Y. Sun, et al.; Mol. Cell. Biol.
20
, 4411 (2000)
Abstract
;
Full Text
Effect of myriocin on plasma sphingolipid metabolism and atherosclerosis in apoE-deficient mice:
M.R. Hojjati, et al.; J. Biol. Chem.
280
, 10284 (2005)
Abstract
Serine palmitoyltransferase inhibitor suppresses HCV replication in a mouse model:
T. Umehara, et al.; BBRC
346
, 67 (2006)
Abstract
Related Products
ALX-420-043
FTY720
Further Categories Containing This Product:
Sphingolipids & Glycosphingolipids Other Products
•
Natural Products - Antiviral / anti-HIV Agents
•
Natural Products - Apoptosis Inducers & Inhibitors
ALX-350-228
Revised 08-Jul-08
Nomilin
PRODUCT LINE
Natural Products / Antibiotics
PRODUCT CATEGORY
Natural Products - Chemopreventive Agents
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ALX-350-228-M025
25 mg
105.00 USD
Product Specification
FORMULA:
C
28
H
34
O
9
MW:
514.6
CAS NUMBER:
1063-77-0
MERCK INDEX:
14:
6674
SOURCE/HOST:
Isolated from grapefruit seed and citrus juice.
PURITY:
≥98% (HPLC)
APPEARANCE:
White to off-white solid.
SOLUBILITY:
Soluble in acetone; slightly soluble in 100% ethanol, methanol, isopropanol or ethyl acetate; insoluble in water.
SHIPPING:
AMBIENT
LONG TERM STORAGE:
+20°C
Product Description
Induces phase II detoxifying enzymes and inhibits chemically induced carcinogenesis. Exhibits immunomodulatory activity and also inhibits HIV-1 replication. Does not possess any inherent antioxidant capacity.
Product Specific Literature References
V.P. Maier, et al.; ACS Symposium Series
143
, 63 (1980)
Inhibition of benzo[a]pyrene-induced forestomach neoplasia in mice by citrus limonoids:
L.K.T. Lam & S. Hasegawa; Nutr. Cancer
12
, 43 (1989)
Abstract
The effect of citrus limonoids on hamster buccal pouch carcinogenesis:
E.G. Miller, et al.; Carcinogenesis
10
, 1535 (1989)
Abstract
Effect of naturally occurring triterpenoids glycyrrhizic acid, ursolic acid, oleanolic acid and nomilin on the immune system:
T.J. Raphael & G. Kuttan; Phytomedicine
10
, 483 (2003)
Abstract
Effect of limonin and nomilin on HIV-1 replication on infected human mononuclear cells:
L. Battinelli, et al.; Planta Med.
69
, 910 (2003)
Abstract
Evaluation of the antioxidant capacity of limonin, nomilin, and limonin glucoside:
A.P. Breksa, 3rd & G.D. Manners; J. Agric. Food Chem.
54
, 3827 (2006)
Abstract
Further Categories Containing This Product:
Antitumor Agents (Enzyme Activators & Inducers)
•
Natural Products - Immunomodulators
•
Natural Products - Antiviral / anti-HIV Agents
•
Active Substances from Fruit and Vegetables
ALX-350-276
Revised 16-Jun-08
Pseudohypericin
PRODUCT LINE
Natural Products / Antibiotics
PRODUCT CATEGORY
Natural Products - Protein Kinase Inhibitors
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ALX-350-276-M001
1 mg
115.00 USD
ALX-350-276-M005
5 mg
460.00 USD
Product Specification
FORMULA:
C
30
H
16
O
9
MW:
520.5
CAS NUMBER:
55954-61-5
SOURCE/HOST:
Isolated from
Hypericum perforatum
.
PURITY:
≥98%
APPEARANCE:
Black to black-red powder.
SOLUBILITY:
Soluble in methanol, 100% ethanol, DMSO, acetone and other organic solvents.
SHIPPING:
AMBIENT
LONG TERM STORAGE:
+4°C
HANDLING:
Protect from light.
HAZARD:
HARMFUL.
Product Description
Inhibitor of protein kinase C (PKC) (IC
50
=15µg/ml). Antiviral and antiretroviral activity. Potent inhibitor of dopamine-β-hydrolase (IC
50
=3µg/ml).
Product Specific Literature References
Zur Isolierung und Konstitution des Pseudohypericins :
H. Brockmann, et al.; Tetrahedron Lett.
15
, 1991 (1974)
Therapeutic agents with dramatic antiretroviral activity and little toxicity at effective doses: aromatic polycyclic diones hypericin and pseudohypericin:
D. Meruelo, et al.; PNAS
85
, 5230 (1988)
Abstract
Studies of the mechanisms of action of the antiretroviral agents hypericin and pseudohypericin:
G. Lavie, et al.; PNAS
86
, 5963 (1989)
Abstract
Hypericin and pseudohypericin specifically inhibit protein kinase C: possible relation to their antiretroviral activity:
I. Takahashi, et al.; BBRC
165
, 1207 (1989)
Abstract
Biochemical activities of extracts from Hypericum perforatum L. 5th communication: dopamine-beta-hydroxylase-product quantification by HPLC and inhibition by hypericins and flavonoids:
A. Denke, et al.; Arzneimittelforschung
50
, 415 (2000)
Abstract
Antagonist effect of pseudohypericin at CRF1 receptors:
U. Simmen, et al.; Eur. J. Pharmacol.
458
, 251 (2003)
Abstract
Phototoxic and apoptosis-inducing capacity of pseudohypericin:
C.M. Schempp, et al.; Planta Med.
68
, 171 (2002)
Abstract
Further Categories Containing This Product:
PKC Inhibitors
•
Natural Products - Antiviral / anti-HIV Agents
•
Natural Products for Neurological Research
•
Neuroactive Agents Other Products
ALX-350-364
Revised 08-Apr-08
Psoralen
SYNONYMS
Ficusin
7
H
-Furo[3,2-g]benzopyran-7-one
PRODUCT LINE
Natural Products / Antibiotics
PRODUCT CATEGORY
Natural Products with Antibiotic Activity
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ALX-350-364-M025
25 mg
95.00 USD
ALX-350-364-M100
100 mg
285.00 USD
Product Specification
FORMULA:
C
11
H
6
O
3
MW:
186.2
CAS NUMBER:
66-97-7
MERCK INDEX:
14:
7928
RTECS:
LV0944000
SOURCE/HOST:
Isolated from
Psoralea corylifolia
.
PURITY:
≥98% (HPLC)
APPEARANCE:
White to off-white crystalline solid.
SOLUBILITY:
Soluble in ethyl acetate or acetone; insoluble in water.
SHIPPING:
AMBIENT
LONG TERM STORAGE:
-20°C
HAZARD:
MAY BE MUTAGENIC. HARMFUL.
Product Description
Shows antiviral, antibacterial, antifungal and insecticidal properties. Binds DNA through single and double-stranded cross-linking after photoactivation. Used as photochemical probe in studies of DNA mutation and repair mechanisms. Causes photosensitization in human.
Product Specific Literature References
Psoralen phototoxicity: correlation with serum and epidermal 8-methoxypsoralen and 5-methoxypsoralen in the guinea pig:
A. Kornhauser, et al.; Science
217
, 733 (1982)
Abstract
Psoralens as photoactive probes of nucleic acid structure and function: organic chemistry, photochemistry, and biochemistry:
G.D. Cimino, et al.; Annu. Rev. Biochem.
54
, 1151 (1985), (Review)
Abstract
Electron microscopic identification of supercoiled regions in complex DNA structures:
R.B. Inman & M. Schnos; J. Mol. Biol.
193
, 377 (1987)
Abstract
Probing DNA structure with psoralen in vitro:
D.W. Ussery, et al.; Meth. Enzymol.
212
, 242 (1992)
Abstract
DNA interstrand cross-links induced by psoralen are not repaired in mammalian mitochondria:
C. Cullinane & V.A. Bohr; Cancer Res.
58
, 1400 (1998)
Abstract
;
Full Text
Psoralen photocrosslinking, a tool to study the chromatin structure of RNA polymerase I--transcribed ribosomal genes:
M. Toussaint, et al.; Biochem. Cell Biol.
83
, 449 (2005)
Abstract
Psoralen-induced DNA adducts are substrates for the base excision repair pathway in human cells:
S. Couve-Privat, et al.; Nucl. Acids Res.
35
, 5672 (2007)
Abstract
;
Full Text
Site-directed gene mutation at mixed sequence targets by psoralen-conjugated pseudo-complementary peptide nucleic acids:
K.H. Kim, et al.; Nucl. Acids Res.
35
, 7604 (2007)
Abstract
;
Full Text
Further Categories Containing This Product:
Natural Products - Antiviral / anti-HIV Agents
•
Natural Products - Antifungal Agents
•
DNA Intercalators & Crosslinkers
•
Pesticides / Related Products
ALX-350-296
Revised 30-Jun-08
Thalassiolin B
PRODUCT LINE
Natural Products / Antibiotics
PRODUCT CATEGORY
Natural Products - Antiviral / anti-HIV Agents
Ordering Information
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Format:
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ALX-350-296-MC05
0.5 mg
130.00 USD
Product Specification
FORMULA:
C
22
H
22
O
14
S
MW:
542.5
SOURCE/HOST:
Isolated from
Thalassia testudinum
.
PURITY:
≥98% (HPLC)
APPEARANCE:
Yellow to green oil.
SOLUBILITY:
Soluble in 100% ethanol or DMSO.
LONG TERM STORAGE:
-20°C
HANDLING:
Protect from light.
Product Description
Inhibitor of HIV cDNA integrase.
Product Specific Literature References
Thalassiolins A-C: new marine-derived inhibitors of HIV cDNA integrase
:
D.C. Rowley, et al.; Bioorg. Med. Chem.
10
, 3619 (2002)
Abstract