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Reference: RM17609
€0.00 (tax incl.)
The spike (S) glycoprotein of coronaviruses contains protrusions that will only bind to certain receptors on the host cell. The spike is essential for both host specificity and viral infectivity. The spike (S)...

Reference: RM17624
€0.00 (tax incl.)

Reference: RM17623
€0.00 (tax incl.)

Reference: RM17620
€0.00 (tax incl.)
The spike (S) glycoprotein of coronaviruses contains protrusions that will only bind to certain receptors on the host cell. The spike is essential for both host specificity and viral infectivity. The spike (S)...

Reference: RM17619
€0.00 (tax incl.)
The spike (S) glycoprotein of coronaviruses contains protrusions that will only bind to certain receptors on the host cell. The spike is essential for both host specificity and viral infectivity. The spike (S)...

Reference: RM17608
€0.00 (tax incl.)
The spike (S) glycoprotein of coronaviruses contains protrusions that will only bind to certain receptors on the host cell. The spike is essential for both host specificity and viral infectivity. The spike (S)...
(+)-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
(+)-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
(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)-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...
(S)-(-)-Linoleyl-1'-Hydroxy-2'-Propylamide (S)-(-)-Linoleyl-1'-Hydroxy-2'-Propylamide

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

Reference: 9001236-5
€0.00 (tax incl.)
A homolog of LOEA, characterized by the addition of an (S)-α-methyl group at the methylene carbon adjacent to the amide nitrogen
(S)-(-)-Linoleyl-1'-Hydroxy-2'-Propylamide (S)-(-)-Linoleyl-1'-Hydroxy-2'-Propylamide

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

Reference: 9001236-10
€0.00 (tax incl.)
A homolog of LOEA, characterized by the addition of an (S)-α-methyl group at the methylene carbon adjacent to the amide nitrogen

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