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(+)-15-epi Cloprostenol (+)-15-epi Cloprostenol

(+)-15-epi Cloprostenol

Reference: 10006692-500
€0.00 (tax incl.)
Cloprostenol is a synthetic PGF2α analog and a potent FP receptor agonist. (+)-15-epi Cloprostenol is the 15(S), or 15β-hydroxy enantiomer of (+)-cloprostenol. This epimer is less active by several orders of magnitude...
(+)-15-epi Cloprostenol (+)-15-epi Cloprostenol

(+)-15-epi Cloprostenol

Reference: 10006692-5
€0.00 (tax incl.)
Cloprostenol is a synthetic PGF2α analog and a potent FP receptor agonist. (+)-15-epi Cloprostenol is the 15(S), or 15β-hydroxy enantiomer of (+)-cloprostenol. This epimer is less active by several orders of magnitude...
(+)-15-epi Cloprostenol (+)-15-epi Cloprostenol

(+)-15-epi Cloprostenol

Reference: 10006692-10
€0.00 (tax incl.)
Cloprostenol is a synthetic PGF2α analog and a potent FP receptor agonist. (+)-15-epi Cloprostenol is the 15(S), or 15β-hydroxy enantiomer of (+)-cloprostenol. This epimer is less active by several orders of magnitude...
(+)-15-epi Cloprostenol (+)-15-epi Cloprostenol

(+)-15-epi Cloprostenol

Reference: 10006692-1
€0.00 (tax incl.)
Cloprostenol is a synthetic PGF2α analog and a potent FP receptor agonist. (+)-15-epi Cloprostenol is the 15(S), or 15β-hydroxy enantiomer of (+)-cloprostenol. This epimer is less active by several orders of magnitude...
(+)-5-trans Cloprostenol (+)-5-trans Cloprostenol

(+)-5-trans Cloprostenol

Reference: 10004970-5
€0.00 (tax incl.)
A minor impurity produced in the synthesis of (+)-cloprostenol; 20-fold less active than (+)-cloprostenol in terminating pregnancy in the hamster
(+)-5-trans Cloprostenol (+)-5-trans Cloprostenol

(+)-5-trans Cloprostenol

Reference: 10004970-25
€0.00 (tax incl.)
A minor impurity produced in the synthesis of (+)-cloprostenol; 20-fold less active than (+)-cloprostenol in terminating pregnancy in the hamster
(+)-5-trans Cloprostenol (+)-5-trans Cloprostenol

(+)-5-trans Cloprostenol

Reference: 10004970-10
€0.00 (tax incl.)
A minor impurity produced in the synthesis of (+)-cloprostenol; 20-fold less active than (+)-cloprostenol in terminating pregnancy in the hamster
(+)-5-trans Cloprostenol (+)-5-trans Cloprostenol

(+)-5-trans Cloprostenol

Reference: 10004970-1
€0.00 (tax incl.)
A minor impurity produced in the synthesis of (+)-cloprostenol; 20-fold less active than (+)-cloprostenol in terminating pregnancy in the hamster
(+)-Aphidicolin (+)-Aphidicolin

(+)-Aphidicolin

Reference: BVT-0307-M025
€0.00 (tax incl.)
Phytotoxin. Antibiotic. Antiviral and antineoplastic agent. Antileishmanial agent. Reversible inhibitor of eukaryotic nuclear DNA replication. Useful for cell synchronization. Blocks the cell cycle at G1/S phase....
(+)-Aphidicolin (+)-Aphidicolin

(+)-Aphidicolin

Reference: BVT-0307-M005
€0.00 (tax incl.)
Phytotoxin. Antibiotic. Antiviral and antineoplastic agent. Antileishmanial agent. Reversible inhibitor of eukaryotic nuclear DNA replication. Useful for cell synchronization. Blocks the cell cycle at G1/S phase....
(+)-Aphidicolin (+)-Aphidicolin

(+)-Aphidicolin

Reference: BVT-0307-M001
€0.00 (tax incl.)
Phytotoxin. Antibiotic. Antiviral and antineoplastic agent. Antileishmanial agent. Reversible inhibitor of eukaryotic nuclear DNA replication. Useful for cell synchronization. Blocks the cell cycle at G1/S phase....
(+)-Brefeldin A (+)-Brefeldin A

(+)-Brefeldin A

Reference: BVT-0190-M001
€0.00 (tax incl.)
Protein transport from ER to Golgi inhibitor. ADP-ribosylation factor (Arf) inhibitor. Cytotoxic. Antibiotic. Antiviral. Apoptosis inducer. Antitumor compound. Intracellular collagen degradation inhibitor Reviews.
(+)-Brefeldin A (+)-Brefeldin A

(+)-Brefeldin A

Reference: AG-CN2-0018-M025
€0.00 (tax incl.)
Protein transport from ER to Golgi inhibitor. ADP-ribosylation factor (Arf) inhibitor. Cytotoxic. Antibiotic. Antiviral. Apoptosis inducer. Antitumor compound. Intracellular collagen degradation inhibitor. Reviews.
(+)-Brefeldin A (+)-Brefeldin A

(+)-Brefeldin A

Reference: AG-CN2-0018-M010
€0.00 (tax incl.)
Protein transport from ER to Golgi inhibitor. ADP-ribosylation factor (Arf) inhibitor. Cytotoxic. Antibiotic. Antiviral. Apoptosis inducer. Antitumor compound. Intracellular collagen degradation inhibitor. Reviews.
(+)-Brefeldin A (+)-Brefeldin A

(+)-Brefeldin A

Reference: AG-CN2-0018-M005
€0.00 (tax incl.)
Protein transport from ER to Golgi inhibitor. ADP-ribosylation factor (Arf) inhibitor. Cytotoxic. Antibiotic. Antiviral. Apoptosis inducer. Antitumor compound. Intracellular collagen degradation inhibitor. Reviews.
(+)-Cloprostenol (+)-Cloprostenol

(+)-Cloprostenol

Reference: 16765-5
€0.00 (tax incl.)
A synthetic analog of PGF2α; an FP receptor agonist and a potent luteolytic agent in rats and hamsters; the optically active, 15(R) enantiomer of cloprostenol responsible for the majority of its biological activity
(+)-Cloprostenol (+)-Cloprostenol

(+)-Cloprostenol

Reference: 16765-10
€0.00 (tax incl.)
A synthetic analog of PGF2α; an FP receptor agonist and a potent luteolytic agent in rats and hamsters; the optically active, 15(R) enantiomer of cloprostenol responsible for the majority of its biological activity
(+)-Cloprostenol (+)-Cloprostenol

(+)-Cloprostenol

Reference: 16765-1
€0.00 (tax incl.)
A synthetic analog of PGF2α; an FP receptor agonist and a potent luteolytic agent in rats and hamsters; the optically active, 15(R) enantiomer of cloprostenol responsible for the majority of its biological activity
(+)-Cloprostenol (sodium salt) (+)-Cloprostenol (sodium salt)

(+)-Cloprostenol (sodium salt)

Reference: 16766-5
€0.00 (tax incl.)
(+)-Cloprostenol (sodium salt) is a more water soluble, crystalline form of (+)-cloprostenol.
(+)-Cloprostenol (sodium salt) (+)-Cloprostenol (sodium salt)

(+)-Cloprostenol (sodium salt)

Reference: 16766-10
€0.00 (tax incl.)
(+)-Cloprostenol (sodium salt) is a more water soluble, crystalline form of (+)-cloprostenol.
(+)-Cloprostenol (sodium salt) (+)-Cloprostenol (sodium salt)

(+)-Cloprostenol (sodium salt)

Reference: 16766-1
€0.00 (tax incl.)
(+)-Cloprostenol (sodium salt) is a more water soluble, crystalline form of (+)-cloprostenol.
(+)-Cloprostenol isopropyl ester (+)-Cloprostenol isopropyl ester

(+)-Cloprostenol isopropyl ester

Reference: 10010016-5
€0.00 (tax incl.)
A synthetic analog of PGF2α; an FP receptor agonist and a potent luteolytic agent in rats and hamsters; the optically active, 15(R) enantiomer of cloprostenol responsible for the majority of its biological activity; a...
(+)-Cloprostenol isopropyl ester (+)-Cloprostenol isopropyl ester

(+)-Cloprostenol isopropyl ester

Reference: 10010016-10
€0.00 (tax incl.)
A synthetic analog of PGF2α; an FP receptor agonist and a potent luteolytic agent in rats and hamsters; the optically active, 15(R) enantiomer of cloprostenol responsible for the majority of its biological activity; a...
(+)-Cloprostenol isopropyl ester (+)-Cloprostenol isopropyl ester

(+)-Cloprostenol isopropyl ester

Reference: 10010016-1
€0.00 (tax incl.)
A synthetic analog of PGF2α; an FP receptor agonist and a potent luteolytic agent in rats and hamsters; the optically active, 15(R) enantiomer of cloprostenol responsible for the majority of its biological activity; a...
(+)-Cloprostenol methyl amide (+)-Cloprostenol methyl amide

(+)-Cloprostenol methyl amide

Reference: 10010495-5
€0.00 (tax incl.)
A more lipid soluble form of (+)-cloprostenol, possibly serving as a prodrug for the bioactive free acid
(+)-Cloprostenol methyl amide (+)-Cloprostenol methyl amide

(+)-Cloprostenol methyl amide

Reference: 10010495-10
€0.00 (tax incl.)
A more lipid soluble form of (+)-cloprostenol, possibly serving as a prodrug for the bioactive free acid
(+)-Cloprostenol methyl amide (+)-Cloprostenol methyl amide

(+)-Cloprostenol methyl amide

Reference: 10010495-1
€0.00 (tax incl.)
A more lipid soluble form of (+)-cloprostenol, possibly serving as a prodrug for the bioactive free acid
(+)-Cloprostenol methyl ester (+)-Cloprostenol methyl ester

(+)-Cloprostenol methyl ester

Reference: 10010115-5
€0.00 (tax incl.)
A more lipid soluble form of (+)-cloprostenol, amenable for certain formulations
(+)-Cloprostenol methyl ester (+)-Cloprostenol methyl ester

(+)-Cloprostenol methyl ester

Reference: 10010115-10
€0.00 (tax incl.)
A more lipid soluble form of (+)-cloprostenol, amenable for certain formulations
(+)-Cloprostenol methyl ester (+)-Cloprostenol methyl ester

(+)-Cloprostenol methyl ester

Reference: 10010115-1
€0.00 (tax incl.)
A more lipid soluble form of (+)-cloprostenol, amenable for certain formulations
(+)-Flavipucine (+)-Flavipucine

(+)-Flavipucine

Reference: BVT-0279-M001
€0.00 (tax incl.)
Phytotoxin (Fruit rot toxin). Antibiotic. Antibacterial and antifungal compound.
(+)-Limonene (+)-Limonene

(+)-Limonene

Reference: 21719-5
€0.00 (tax incl.)
A monocyclic monoterpene with diverse biological activities; inhibits the growth of bacteria including S. aureus, B. cereus, E. faecalis, E. coli, P. aeruginosa, K. pneumoniae, M. catarrhalis, and C. neoformans (MICs...
(+)-Limonene (+)-Limonene

(+)-Limonene

Reference: 21719-1
€0.00 (tax incl.)
A monocyclic monoterpene with diverse biological activities; inhibits the growth of bacteria including S. aureus, B. cereus, E. faecalis, E. coli, P. aeruginosa, K. pneumoniae, M. catarrhalis, and C. neoformans (MICs...
(+)-Rubiginone B2 (+)-Rubiginone B2

(+)-Rubiginone B2

Reference: BVT-0026-M001
€0.00 (tax incl.)
Angucyclinone antibiotic. Antibacterial and antitumor agent. Potentiates the cytotoxicity of vincristine. Antimalarial agent.
(-)-Viriditoxin (-)-Viriditoxin

(-)-Viriditoxin

Reference: AG-CN2-0471-C500
€0.00 (tax incl.)
Antibiotic. Exhibits broad activity against Gram-positive bacteria. Bacterial cell division protein FtsZ inhibitor (IC50=8.2µg/ml). Inhibits the GTPase activity of FtsZ in vitro (IC50=7.0µg/ml). Induces apoptosis and...
(E)-2-Hexadecenal (E)-2-Hexadecenal

(E)-2-Hexadecenal

Reference: 17566-500
€0.00 (tax incl.)
A sphingolipid degradation product that has been shown to induce cytoskeletal reorganization and eventual apoptosis via a JNK-dependent pathway; reacts readily with deoxyguanosine and DNA to form aldehyde-derived DNA...
(E)-2-Hexadecenal (E)-2-Hexadecenal

(E)-2-Hexadecenal

Reference: 17566-5
€0.00 (tax incl.)
A sphingolipid degradation product that has been shown to induce cytoskeletal reorganization and eventual apoptosis via a JNK-dependent pathway; reacts readily with deoxyguanosine and DNA to form aldehyde-derived DNA...
(E)-2-Hexadecenal (E)-2-Hexadecenal

(E)-2-Hexadecenal

Reference: 17566-1
€0.00 (tax incl.)
A sphingolipid degradation product that has been shown to induce cytoskeletal reorganization and eventual apoptosis via a JNK-dependent pathway; reacts readily with deoxyguanosine and DNA to form aldehyde-derived DNA...
(R)-(+)-Linoleyl-1'-Hydroxy-2'-Propylamide (R)-(+)-Linoleyl-1'-Hydroxy-2'-Propylamide

(R)-(+)-Linoleyl-1'-Hydroxy-2'-Propylamide

Reference: 9001233-5
€0.00 (tax incl.)
A homolog of LOEA, characterized by the addition of an (R)-α-methyl group at the methylene carbon adjacent to the amide nitrogen
(R)-(+)-Linoleyl-1'-Hydroxy-2'-Propylamide (R)-(+)-Linoleyl-1'-Hydroxy-2'-Propylamide

(R)-(+)-Linoleyl-1'-Hydroxy-2'-Propylamide

Reference: 9001233-10
€0.00 (tax incl.)
A homolog of LOEA, characterized by the addition of an (R)-α-methyl group at the methylene carbon adjacent to the amide nitrogen
(R)-(+)-Linoleyl-1'-Hydroxy-2'-Propylamide (R)-(+)-Linoleyl-1'-Hydroxy-2'-Propylamide

(R)-(+)-Linoleyl-1'-Hydroxy-2'-Propylamide

Reference: 9001233-1
€0.00 (tax incl.)
A homolog of LOEA, characterized by the addition of an (R)-α-methyl group at the methylene carbon adjacent to the amide nitrogen
(R)-(-)-Linoleyl-2'-Hydroxy-1'-Propylamide (R)-(-)-Linoleyl-2'-Hydroxy-1'-Propylamide

(R)-(-)-Linoleyl-2'-Hydroxy-1'-Propylamide

Reference: 9001234-5
€0.00 (tax incl.)
A homolog of LOEA, characterized by the addition of an (R)-α-methyl group at the methylene carbon adjacent to the amide nitrogen
(R)-(-)-Linoleyl-2'-Hydroxy-1'-Propylamide (R)-(-)-Linoleyl-2'-Hydroxy-1'-Propylamide

(R)-(-)-Linoleyl-2'-Hydroxy-1'-Propylamide

Reference: 9001234-10
€0.00 (tax incl.)
A homolog of LOEA, characterized by the addition of an (R)-α-methyl group at the methylene carbon adjacent to the amide nitrogen
(R)-(-)-Linoleyl-2'-Hydroxy-1'-Propylamide (R)-(-)-Linoleyl-2'-Hydroxy-1'-Propylamide

(R)-(-)-Linoleyl-2'-Hydroxy-1'-Propylamide

Reference: 9001234-1
€0.00 (tax incl.)
A homolog of LOEA, characterized by the addition of an (R)-α-methyl group at the methylene carbon adjacent to the amide nitrogen
(R)-3-hydroxy Myristic Acid (R)-3-hydroxy Myristic Acid

(R)-3-hydroxy Myristic Acid

Reference: 16871-50
€0.00 (tax incl.)
A form of the myristic acid that is found in the lipid A component of some Gram negative bacteria, including Escherichia, Haemophilus, Actinobacillus, and Campylobacter species.
(R)-3-hydroxy Myristic Acid (R)-3-hydroxy Myristic Acid

(R)-3-hydroxy Myristic Acid

Reference: 16871-25
€0.00 (tax incl.)
A form of the myristic acid that is found in the lipid A component of some Gram negative bacteria, including Escherichia, Haemophilus, Actinobacillus, and Campylobacter species.
(R)-3-hydroxy Myristic Acid (R)-3-hydroxy Myristic Acid

(R)-3-hydroxy Myristic Acid

Reference: 16871-100
€0.00 (tax incl.)
A form of the myristic acid that is found in the lipid A component of some Gram negative bacteria, including Escherichia, Haemophilus, Actinobacillus, and Campylobacter species.
(R)-3-hydroxy Myristic Acid (R)-3-hydroxy Myristic Acid

(R)-3-hydroxy Myristic Acid

Reference: 16871-10
€0.00 (tax incl.)
A form of the myristic acid that is found in the lipid A component of some Gram negative bacteria, including Escherichia, Haemophilus, Actinobacillus, and Campylobacter species.
(R)-Butaprost (R)-Butaprost

(R)-Butaprost

Reference: 13745-5
€0.00 (tax incl.)
Butaprost is a structural analog of PGE2 with good selectivity for the EP2 receptor subtype. Butaprost has frequently been used to pharmacologically define the EP receptor expression profile of various human and...
(R)-Butaprost (R)-Butaprost

(R)-Butaprost

Reference: 13745-10
€0.00 (tax incl.)
Butaprost is a structural analog of PGE2 with good selectivity for the EP2 receptor subtype. Butaprost has frequently been used to pharmacologically define the EP receptor expression profile of various human and...
(R)-Butaprost (R)-Butaprost

(R)-Butaprost

Reference: 13745-1
€0.00 (tax incl.)
Butaprost is a structural analog of PGE2 with good selectivity for the EP2 receptor subtype. Butaprost has frequently been used to pharmacologically define the EP receptor expression profile of various human and...
(R)-Butaprost (free acid) (R)-Butaprost (free acid)

(R)-Butaprost (free acid)

Reference: 10006045-500
€0.00 (tax incl.)
Butaprost is a structural analog of PGE2 with good selectivity for the EP2 receptor subtype. Butaprost has frequently been used to pharmacologically define the EP receptor expression profile of various human and...
(R)-Butaprost (free acid) (R)-Butaprost (free acid)

(R)-Butaprost (free acid)

Reference: 10006045-5
€0.00 (tax incl.)
Butaprost is a structural analog of PGE2 with good selectivity for the EP2 receptor subtype. Butaprost has frequently been used to pharmacologically define the EP receptor expression profile of various human and...
(R)-Butaprost (free acid) (R)-Butaprost (free acid)

(R)-Butaprost (free acid)

Reference: 10006045-10
€0.00 (tax incl.)
Butaprost is a structural analog of PGE2 with good selectivity for the EP2 receptor subtype. Butaprost has frequently been used to pharmacologically define the EP receptor expression profile of various human and...
(R)-Butaprost (free acid) (R)-Butaprost (free acid)

(R)-Butaprost (free acid)

Reference: 10006045-1
€0.00 (tax incl.)
Butaprost is a structural analog of PGE2 with good selectivity for the EP2 receptor subtype. Butaprost has frequently been used to pharmacologically define the EP receptor expression profile of various human and...
(R)-Semivioxanthin (R)-Semivioxanthin

(R)-Semivioxanthin

Reference: BVT-0360-M001
€0.00 (tax incl.)
Mycotoxin. Antibacterial (Gram-positive) and antifungal. Immunoregulator by degradation of IkappaB (Inhibitor of NF-kappaB) and regulation of the TNF-alpha (tumor necrosis factor-alpha) and MAPK (mitogen-activated...
(R)-Semivioxanthin (R)-Semivioxanthin

(R)-Semivioxanthin

Reference: BVT-0360-C500
€0.00 (tax incl.)
Mycotoxin. Antibacterial (Gram-positive) and antifungal. Immunoregulator by degradation of IkappaB (Inhibitor of NF-kappaB) and regulation of the TNF-alpha (tumor necrosis factor-alpha) and MAPK (mitogen-activated...
(R)-Semixanthomegnin (R)-Semixanthomegnin

(R)-Semixanthomegnin

Reference: BVT-0366-M001
€0.00 (tax incl.)
Antibacterial mycotoxin derivative. Monomer (half) of the genotoxic mycotoxin xanthomegnin.
(R)-Semixanthomegnin (R)-Semixanthomegnin

(R)-Semixanthomegnin

Reference: BVT-0366-C500
€0.00 (tax incl.)
Antibacterial mycotoxin derivative. Monomer (half) of the genotoxic mycotoxin xanthomegnin.
(R)-α-Lipoic Acid (R)-α-Lipoic Acid

(R)-α-Lipoic Acid

Reference: 27299-5
€0.00 (tax incl.)
A cyclic disulfide antioxidant; acts as a cofactor in 2-oxo dehydrogenase complex reactions and is reduced to DHLA; decreases serum levels of MDA and increases the activity of SOD and T-AOC in a mouse model of...
(R)-α-Lipoic Acid (R)-α-Lipoic Acid

(R)-α-Lipoic Acid

Reference: 27299-25
€0.00 (tax incl.)
A cyclic disulfide antioxidant; acts as a cofactor in 2-oxo dehydrogenase complex reactions and is reduced to DHLA; decreases serum levels of MDA and increases the activity of SOD and T-AOC in a mouse model of...
(R)-α-Lipoic Acid (R)-α-Lipoic Acid

(R)-α-Lipoic Acid

Reference: 27299-10
€0.00 (tax incl.)
A cyclic disulfide antioxidant; acts as a cofactor in 2-oxo dehydrogenase complex reactions and is reduced to DHLA; decreases serum levels of MDA and increases the activity of SOD and T-AOC in a mouse model of...
(R)-α-Lipoic Acid (R)-α-Lipoic Acid

(R)-α-Lipoic Acid

Reference: 27299-1
€0.00 (tax incl.)
A cyclic disulfide antioxidant; acts as a cofactor in 2-oxo dehydrogenase complex reactions and is reduced to DHLA; decreases serum levels of MDA and increases the activity of SOD and T-AOC in a mouse model of...
(R,R)-Hymeglusin (R,R)-Hymeglusin

(R,R)-Hymeglusin

Reference: AG-CN2-0103-MM25
€0.00 (tax incl.)
beta-Lactone antibiotic. Antibacterial and antifungal. Specific and irreversible inhibitor of 3-hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) synthase in vitro and in vivo by covalently modifying the active Cys129...
(R,R)-Hymeglusin (R,R)-Hymeglusin

(R,R)-Hymeglusin

Reference: AG-CN2-0103-M001
€0.00 (tax incl.)
beta-Lactone antibiotic. Antibacterial and antifungal. Specific and irreversible inhibitor of 3-hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) synthase in vitro and in vivo by covalently modifying the active Cys129...
(R,R)-Hymeglusin (R,R)-Hymeglusin

(R,R)-Hymeglusin

Reference: AG-CN2-0103-MC05
€0.00 (tax incl.)
beta-Lactone antibiotic. Antibacterial and antifungal. Specific and irreversible inhibitor of 3-hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) synthase in vitro and in vivo by covalently modifying the active Cys129...
(S)-(+)-Ascochin (S)-(+)-Ascochin

(S)-(+)-Ascochin

Reference: BVT-0309-M005
€0.00 (tax incl.)
Antibiotic. Antifungal and phytotoxic.
(S)-(+)-Ascochin (S)-(+)-Ascochin

(S)-(+)-Ascochin

Reference: BVT-0309-M001
€0.00 (tax incl.)
Antibiotic. Antifungal and phytotoxic.

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