MedChem Express

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MedChemExpress has an experienced team of custom synthesis chemists, led by an impressive group of Ph.D.'s. With this team, we have the capability of supporting all kinds of chemistry projects of multiple step syntheses of complex labeled molecules, including metabolites and steroids. Following scientific and technological innovation, challenging traditional thinking, MedChemExpress has always been committed to develop quality products that exceed international standards on cost and reliability, to create the most advanced synthetic route. With high experiences in preparing a large numbers of different biologically active molecules, we provide rapid synthesis of new products. That is why we can consistently deliver your custom synthesis compounds faster than any other company.

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(-)-(S)-Equol 5mg  | ≥98%

MedChem Express

(-)-(S)-Equol is a high affinity ligand for estrogen receptor β with a Ki of 0.73 nM. IC50 & Target: Ki: 0.73 nM (Estrogen receptor β)[1] In Vitro: (-)-(S)-Equol shows the greatest affinity for ERβ (Ki=0.73±0.2 nM), whereas its affinity for ERα (Ki=6.41±1 nM) is relatively poor[1]. (-)-(S)-Equol inhibits the growth of LnCaP, DU145 and PC3 […]

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(-)-(S)-Equol 10mg  | ≥98%

MedChem Express

(-)-(S)-Equol is a high affinity ligand for estrogen receptor β with a Ki of 0.73 nM. IC50 & Target: Ki: 0.73 nM (Estrogen receptor β)[1] In Vitro: (-)-(S)-Equol shows the greatest affinity for ERβ (Ki=0.73±0.2 nM), whereas its affinity for ERα (Ki=6.41±1 nM) is relatively poor[1]. (-)-(S)-Equol inhibits the growth of LnCaP, DU145 and PC3 […]

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(-)-(S)-Equol 25mg  | ≥98%

MedChem Express

(-)-(S)-Equol is a high affinity ligand for estrogen receptor β with a Ki of 0.73 nM. IC50 & Target: Ki: 0.73 nM (Estrogen receptor β)[1] In Vitro: (-)-(S)-Equol shows the greatest affinity for ERβ (Ki=0.73±0.2 nM), whereas its affinity for ERα (Ki=6.41±1 nM) is relatively poor[1]. (-)-(S)-Equol inhibits the growth of LnCaP, DU145 and PC3 […]

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(-)-(S)-Equol 50mg  | ≥98%

MedChem Express

(-)-(S)-Equol is a high affinity ligand for estrogen receptor β with a Ki of 0.73 nM. IC50 & Target: Ki: 0.73 nM (Estrogen receptor β)[1] In Vitro: (-)-(S)-Equol shows the greatest affinity for ERβ (Ki=0.73±0.2 nM), whereas its affinity for ERα (Ki=6.41±1 nM) is relatively poor[1]. (-)-(S)-Equol inhibits the growth of LnCaP, DU145 and PC3 […]

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(-)-(S)-Equol 10mM/1mL  | ≥98%

MedChem Express

(-)-(S)-Equol is a high affinity ligand for estrogen receptor β with a Ki of 0.73 nM. IC50 & Target: Ki: 0.73 nM (Estrogen receptor β)[1] In Vitro: (-)-(S)-Equol shows the greatest affinity for ERβ (Ki=0.73±0.2 nM), whereas its affinity for ERα (Ki=6.41±1 nM) is relatively poor[1]. (-)-(S)-Equol inhibits the growth of LnCaP, DU145 and PC3 […]

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(-)-Blebbistatin 5mg  | ≥98%

MedChem Express

(-)-Blebbistatin is an S enantiomer of blebbistatin. Blebbistatin is a potent and selective myosin II inhibitor with IC50 values ranging from 0.5 to 5 μM. IC50 & Target: IC50: 0.5 to 5 μM (myosin II)[1] In Vitro: Blebbistatin potently inhibits several striated muscle myosins as well as vertebrate nonmuscle myosin IIA and IIB with IC50 […]

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(-)-Blebbistatin 10mg  | ≥98%

MedChem Express

(-)-Blebbistatin is an S enantiomer of blebbistatin. Blebbistatin is a potent and selective myosin II inhibitor with IC50 values ranging from 0.5 to 5 μM. IC50 & Target: IC50: 0.5 to 5 μM (myosin II)[1] In Vitro: Blebbistatin potently inhibits several striated muscle myosins as well as vertebrate nonmuscle myosin IIA and IIB with IC50 […]

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(-)-Blebbistatin 50mg  | ≥98%

MedChem Express

(-)-Blebbistatin is an S enantiomer of blebbistatin. Blebbistatin is a potent and selective myosin II inhibitor with IC50 values ranging from 0.5 to 5 μM. IC50 & Target: IC50: 0.5 to 5 μM (myosin II)[1] In Vitro: Blebbistatin potently inhibits several striated muscle myosins as well as vertebrate nonmuscle myosin IIA and IIB with IC50 […]

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(-)-Blebbistatin 10mM/1mL  | ≥98%

MedChem Express

(-)-Blebbistatin is an S enantiomer of blebbistatin. Blebbistatin is a potent and selective myosin II inhibitor with IC50 values ranging from 0.5 to 5 μM. IC50 & Target: IC50: 0.5 to 5 μM (myosin II)[1] In Vitro: Blebbistatin potently inhibits several striated muscle myosins as well as vertebrate nonmuscle myosin IIA and IIB with IC50 […]

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(-)-Borneol 10mM/1mL  | ≥98%

MedChem Express

(-)-Borneol has a highly efficacious positive modulating action at GABA receptor with an EC50 of 237 μM. IC50 & Target: EC50: 237 μM (GABA receptor)[1] In Vitro: (-)-Borneol is an enantiomer of (+)-Borneol. (+)-Borneol is a natural bicyclic monoterpene used for analgesia and anesthesia in traditional Chinese medicine; enhances GABA receptor activity with an EC50 […]

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(-)-Borneol 100mg  | ≥98%

MedChem Express

(-)-Borneol has a highly efficacious positive modulating action at GABA receptor with an EC50 of 237 μM. IC50 & Target: EC50: 237 μM (GABA receptor)[1] In Vitro: (-)-Borneol is an enantiomer of (+)-Borneol. (+)-Borneol is a natural bicyclic monoterpene used for analgesia and anesthesia in traditional Chinese medicine; enhances GABA receptor activity with an EC50 […]

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(-)-Catechin gallate 5mg  | ≥98%

MedChem Express

(-)-Catechin gallate is a minor constituent in green tea catechins. (-)-Catechin gallate inhibits the activity of COX-1 and COX-2 enzymes. IC50 & Target: COX-1 and COX-2[1] In Vitro: (-)-Catechin gallate (CG) directly interacts with DNA oligomers and inhibits the activity of COX-1 and COX-2 enzymes, the gene expression of matrix metalloproteinase-9 in macrophage-differentiated HL-60 myeloid […]

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(-)-Catechin gallate 10mg  | ≥98%

MedChem Express

(-)-Catechin gallate is a minor constituent in green tea catechins. (-)-Catechin gallate inhibits the activity of COX-1 and COX-2 enzymes. IC50 & Target: COX-1 and COX-2[1] In Vitro: (-)-Catechin gallate (CG) directly interacts with DNA oligomers and inhibits the activity of COX-1 and COX-2 enzymes, the gene expression of matrix metalloproteinase-9 in macrophage-differentiated HL-60 myeloid […]

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(-)-Catechin gallate 10mM/1mL  | ≥98%

MedChem Express

(-)-Catechin gallate is a minor constituent in green tea catechins. (-)-Catechin gallate inhibits the activity of COX-1 and COX-2 enzymes. IC50 & Target: COX-1 and COX-2[1] In Vitro: (-)-Catechin gallate (CG) directly interacts with DNA oligomers and inhibits the activity of COX-1 and COX-2 enzymes, the gene expression of matrix metalloproteinase-9 in macrophage-differentiated HL-60 myeloid […]

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(-)-Cephaeline (dihydrochloride) 2mg  | ≥98%

MedChem Express

(-)-Cephaeline dihydrochloride is an enantiomer of Cephaeline dihydrochloride. Cephaeline dihydrochloride is a selective CYP2D6 inhibtor with IC50 of 121 μM. IC50 & Target: IC50: 121 μM (CYP2D6)[1] Ki: 54 μM (CYP2D6)[1] In Vitro: CYP2D6 reveals the highest metabolic activity for the generation of 9-O-demethylEmetine, whereas this enzyme also shows a significant metabolic activity for the […]

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(-)-Cephaeline (dihydrochloride) 5mg  | ≥98%

MedChem Express

(-)-Cephaeline dihydrochloride is an enantiomer of Cephaeline dihydrochloride. Cephaeline dihydrochloride is a selective CYP2D6 inhibtor with IC50 of 121 μM. IC50 & Target: IC50: 121 μM (CYP2D6)[1] Ki: 54 μM (CYP2D6)[1] In Vitro: CYP2D6 reveals the highest metabolic activity for the generation of 9-O-demethylEmetine, whereas this enzyme also shows a significant metabolic activity for the […]

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(-)-Cevimeline (hydrochloride hemihydrate) 1mg  | ≥98%

MedChem Express

Cevimeline hydrochloride hemihydrate, a novel muscarinic receptor agonist, is a candidate therapeutic drug for xerostomia in Sjogren’s syndrome. IC50 value: Target: mAChR The general pharmacol. properties of this drug on the gastrointestinal, urinary, and reproductive systems and other tissues were investigated in mice, rats, guinea pigs, rabbits, and dogs. The in vitro metab. of SNI-2011 […]

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(-)-Cevimeline (hydrochloride hemihydrate) 5mg  | ≥98%

MedChem Express

Cevimeline hydrochloride hemihydrate, a novel muscarinic receptor agonist, is a candidate therapeutic drug for xerostomia in Sjogren’s syndrome. IC50 value: Target: mAChR The general pharmacol. properties of this drug on the gastrointestinal, urinary, and reproductive systems and other tissues were investigated in mice, rats, guinea pigs, rabbits, and dogs. The in vitro metab. of SNI-2011 […]

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(-)-Cevimeline (hydrochloride hemihydrate) 10mM/1mL  | ≥98%

MedChem Express

Cevimeline hydrochloride hemihydrate, a novel muscarinic receptor agonist, is a candidate therapeutic drug for xerostomia in Sjogren’s syndrome. IC50 value: Target: mAChR The general pharmacol. properties of this drug on the gastrointestinal, urinary, and reproductive systems and other tissues were investigated in mice, rats, guinea pigs, rabbits, and dogs. The in vitro metab. of SNI-2011 […]

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(-)-DHMEQ 2mg  | ≥98%

MedChem Express

(–)-DHMEQ is a potent NF-κB inhibitor. IC50 & Target: NF-κB[1] In Vitro: (–)-DHMEQ binds to cysteine 38 of RelA and cysteine 144 of RelB. (−)-DHMEQ at concentrations greater than 25 µM inhibits the LTβ-induced nuclear translocation of FLAG-RelB WT, whereas the inhibitory effect of (–)-DHMEQ on the nuclear translocation of FLAG-RelB (C144S) became weaker at the […]

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(-)-DHMEQ 5mg  | ≥98%

MedChem Express

(–)-DHMEQ is a potent NF-κB inhibitor. IC50 & Target: NF-κB[1] In Vitro: (–)-DHMEQ binds to cysteine 38 of RelA and cysteine 144 of RelB. (−)-DHMEQ at concentrations greater than 25 µM inhibits the LTβ-induced nuclear translocation of FLAG-RelB WT, whereas the inhibitory effect of (–)-DHMEQ on the nuclear translocation of FLAG-RelB (C144S) became weaker at the […]

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(-)-DHMEQ 10mg  | ≥98%

MedChem Express

(–)-DHMEQ is a potent NF-κB inhibitor. IC50 & Target: NF-κB[1] In Vitro: (–)-DHMEQ binds to cysteine 38 of RelA and cysteine 144 of RelB. (−)-DHMEQ at concentrations greater than 25 µM inhibits the LTβ-induced nuclear translocation of FLAG-RelB WT, whereas the inhibitory effect of (–)-DHMEQ on the nuclear translocation of FLAG-RelB (C144S) became weaker at the […]

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(-)-DHMEQ 25mg  | ≥98%

MedChem Express

(–)-DHMEQ is a potent NF-κB inhibitor. IC50 & Target: NF-κB[1] In Vitro: (–)-DHMEQ binds to cysteine 38 of RelA and cysteine 144 of RelB. (−)-DHMEQ at concentrations greater than 25 µM inhibits the LTβ-induced nuclear translocation of FLAG-RelB WT, whereas the inhibitory effect of (–)-DHMEQ on the nuclear translocation of FLAG-RelB (C144S) became weaker at the […]

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(-)-DHMEQ 10mM/1mL  | ≥98%

MedChem Express

(–)-DHMEQ is a potent NF-κB inhibitor. IC50 & Target: NF-κB[1] In Vitro: (–)-DHMEQ binds to cysteine 38 of RelA and cysteine 144 of RelB. (−)-DHMEQ at concentrations greater than 25 µM inhibits the LTβ-induced nuclear translocation of FLAG-RelB WT, whereas the inhibitory effect of (–)-DHMEQ on the nuclear translocation of FLAG-RelB (C144S) became weaker at the […]

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(-)-Epicatechin 10mM/1mL  | ≥98%

MedChem Express

(-)-Epicatechin inhibits cyclooxygenase-1 (COX-1) with an IC50 of 3.2 μM. (-)-Epicatechin inhibits the IL-1β-induced expression of iNOS by blocking the nuclear localization of the p65 subunit of NF-κB. IC50 & Target: IC50: 3.2 μM (COX-1)[1] In Vitro: (-)-Epicatechin exhibits >95% inhibitory activity at 70 μg/mL against cyclooxygenase-1 (COX-1) with an IC50 of 3.2 μM[1]. (-)-Epicatechin […]

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(-)-Epicatechin 50mg  | ≥98%

MedChem Express

(-)-Epicatechin inhibits cyclooxygenase-1 (COX-1) with an IC50 of 3.2 μM. (-)-Epicatechin inhibits the IL-1β-induced expression of iNOS by blocking the nuclear localization of the p65 subunit of NF-κB. IC50 & Target: IC50: 3.2 μM (COX-1)[1] In Vitro: (-)-Epicatechin exhibits >95% inhibitory activity at 70 μg/mL against cyclooxygenase-1 (COX-1) with an IC50 of 3.2 μM[1]. (-)-Epicatechin […]

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(-)-Epicatechin 10mg  | ≥98%

MedChem Express

(-)-Epicatechin inhibits cyclooxygenase-1 (COX-1) with an IC50 of 3.2 μM. (-)-Epicatechin inhibits the IL-1β-induced expression of iNOS by blocking the nuclear localization of the p65 subunit of NF-κB. IC50 & Target: IC50: 3.2 μM (COX-1)[1] In Vitro: (-)-Epicatechin exhibits >95% inhibitory activity at 70 μg/mL against cyclooxygenase-1 (COX-1) with an IC50 of 3.2 μM[1]. (-)-Epicatechin […]

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(-)-Epicatechin 100mg  | ≥98%

MedChem Express

(-)-Epicatechin inhibits cyclooxygenase-1 (COX-1) with an IC50 of 3.2 μM. (-)-Epicatechin inhibits the IL-1β-induced expression of iNOS by blocking the nuclear localization of the p65 subunit of NF-κB. IC50 & Target: IC50: 3.2 μM (COX-1)[1] In Vitro: (-)-Epicatechin exhibits >95% inhibitory activity at 70 μg/mL against cyclooxygenase-1 (COX-1) with an IC50 of 3.2 μM[1]. (-)-Epicatechin […]

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(-)-Epicatechin gallate 5mg  | ≥98%

MedChem Express

Epicatechin gallate inhibits cyclooxygenase-1 (COX-1) with an IC50 of 7.5 μM. IC50 & Target: IC50: 7.5 uM (COX-1)[1] In Vitro: Epicatechin gallate exhibits >95% inhibitory activity at 70 μg/mL against cyclooxygenase-1 (COX-1) with an IC50 of 7.5 μM[1]. In Vivo: Epicatechin gallate ((-)-Epicatechin-3-O-gallate, ECG), a component of Rhei Rhizoma, is one of the active components […]

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(-)-Epicatechin gallate 10mg  | ≥98%

MedChem Express

Epicatechin gallate inhibits cyclooxygenase-1 (COX-1) with an IC50 of 7.5 μM. IC50 & Target: IC50: 7.5 uM (COX-1)[1] In Vitro: Epicatechin gallate exhibits >95% inhibitory activity at 70 μg/mL against cyclooxygenase-1 (COX-1) with an IC50 of 7.5 μM[1]. In Vivo: Epicatechin gallate ((-)-Epicatechin-3-O-gallate, ECG), a component of Rhei Rhizoma, is one of the active components […]

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(-)-Epicatechin gallate 25mg  | ≥98%

MedChem Express

Epicatechin gallate inhibits cyclooxygenase-1 (COX-1) with an IC50 of 7.5 μM. IC50 & Target: IC50: 7.5 uM (COX-1)[1] In Vitro: Epicatechin gallate exhibits >95% inhibitory activity at 70 μg/mL against cyclooxygenase-1 (COX-1) with an IC50 of 7.5 μM[1]. In Vivo: Epicatechin gallate ((-)-Epicatechin-3-O-gallate, ECG), a component of Rhei Rhizoma, is one of the active components […]

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(-)-Epicatechin gallate 50mg  | ≥98%

MedChem Express

Epicatechin gallate inhibits cyclooxygenase-1 (COX-1) with an IC50 of 7.5 μM. IC50 & Target: IC50: 7.5 uM (COX-1)[1] In Vitro: Epicatechin gallate exhibits >95% inhibitory activity at 70 μg/mL against cyclooxygenase-1 (COX-1) with an IC50 of 7.5 μM[1]. In Vivo: Epicatechin gallate ((-)-Epicatechin-3-O-gallate, ECG), a component of Rhei Rhizoma, is one of the active components […]

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(-)-Epicatechin gallate 10mM/1mL  | ≥98%

MedChem Express

Epicatechin gallate inhibits cyclooxygenase-1 (COX-1) with an IC50 of 7.5 μM. IC50 & Target: IC50: 7.5 uM (COX-1)[1] In Vitro: Epicatechin gallate exhibits >95% inhibitory activity at 70 μg/mL against cyclooxygenase-1 (COX-1) with an IC50 of 7.5 μM[1]. In Vivo: Epicatechin gallate ((-)-Epicatechin-3-O-gallate, ECG), a component of Rhei Rhizoma, is one of the active components […]

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(-)-Epigallocatechin 5mg  | ≥98%

MedChem Express

(-)-Epigallocatechin is the most abundant flavonoid in green tea, can bind to unfolded native polypeptides and prevent conversion to amyloid fibrils. IC50 value: Target: in vitro: EGCG is a potent inhibitor of amyloidogenic cystatin I66Q amyloid fibril formation in vitro. Computational analysis suggests that EGCG prevents amyloidogenic cystatin fibril formation by stabilizing the molecule in […]

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(-)-Epigallocatechin 10mg  | ≥98%

MedChem Express

(-)-Epigallocatechin is the most abundant flavonoid in green tea, can bind to unfolded native polypeptides and prevent conversion to amyloid fibrils. IC50 value: Target: in vitro: EGCG is a potent inhibitor of amyloidogenic cystatin I66Q amyloid fibril formation in vitro. Computational analysis suggests that EGCG prevents amyloidogenic cystatin fibril formation by stabilizing the molecule in […]

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(-)-Epigallocatechin 10mM/1mL  | ≥98%

MedChem Express

(-)-Epigallocatechin is the most abundant flavonoid in green tea, can bind to unfolded native polypeptides and prevent conversion to amyloid fibrils. IC50 value: Target: in vitro: EGCG is a potent inhibitor of amyloidogenic cystatin I66Q amyloid fibril formation in vitro. Computational analysis suggests that EGCG prevents amyloidogenic cystatin fibril formation by stabilizing the molecule in […]

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(-)-Epigallocatechin Gallate 10mM/1mL  | ≥98%

MedChem Express

(-)-Epigallocatechin Gallate is an antioxidant polyphenol flavonoid form green tea, and inhibits the activation of EGFR, HER2 and HER3, with antitumor activity. IC50 & Target: EGFR, HER2 and HER3[1] In Vitro: (-)-Epigallocatechin Gallate (EGCG) inhibits activation EGFR, HER2 and HER3 in the SW837 human colon cancer cell line. (-)-Epigallocatechin Gallate (10 μM) also inhibits cell […]

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(-)-Epigallocatechin Gallate 50mg  | ≥98%

MedChem Express

(-)-Epigallocatechin Gallate is an antioxidant polyphenol flavonoid form green tea, and inhibits the activation of EGFR, HER2 and HER3, with antitumor activity. IC50 & Target: EGFR, HER2 and HER3[1] In Vitro: (-)-Epigallocatechin Gallate (EGCG) inhibits activation EGFR, HER2 and HER3 in the SW837 human colon cancer cell line. (-)-Epigallocatechin Gallate (10 μM) also inhibits cell […]

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(-)-Epigallocatechin Gallate 100mg  | ≥98%

MedChem Express

(-)-Epigallocatechin Gallate is an antioxidant polyphenol flavonoid form green tea, and inhibits the activation of EGFR, HER2 and HER3, with antitumor activity. IC50 & Target: EGFR, HER2 and HER3[1] In Vitro: (-)-Epigallocatechin Gallate (EGCG) inhibits activation EGFR, HER2 and HER3 in the SW837 human colon cancer cell line. (-)-Epigallocatechin Gallate (10 μM) also inhibits cell […]

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(-)-Fucose 100mg  | ≥98%

MedChem Express

(-)-Fucose is classified as a member of the hexoses, plays a role in A and B blood group antigen substructure determination, selectin-mediated leukocyte-endothelial adhesion, and host-microbe interactions.

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(-)-Fucose 10mM/1mL  | ≥98%

MedChem Express

(-)-Fucose is classified as a member of the hexoses, plays a role in A and B blood group antigen substructure determination, selectin-mediated leukocyte-endothelial adhesion, and host-microbe interactions.

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(-)-Gallocatechin gallate 5mg  | ≥98%

MedChem Express

(-)-Gallocatechin gallate is the polyphenol isolated from tea, with cancer-preventive activities. In Vitro: The amount of (-)-Gallocatechin gallate does not differ in leaves of different stages, and the content is relatively low[1]. (−)-gallocatechin gallate in combination with active catechins ((−)-epigallocatechin gallate) has synergistic effects on the induction of apoptosis and inhibition of cell growth for […]

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(-)-Gallocatechin gallate 10mg  | ≥98%

MedChem Express

(-)-Gallocatechin gallate is the polyphenol isolated from tea, with cancer-preventive activities. In Vitro: The amount of (-)-Gallocatechin gallate does not differ in leaves of different stages, and the content is relatively low[1]. (−)-gallocatechin gallate in combination with active catechins ((−)-epigallocatechin gallate) has synergistic effects on the induction of apoptosis and inhibition of cell growth for […]

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(-)-Gallocatechin gallate 25mg  | ≥98%

MedChem Express

(-)-Gallocatechin gallate is the polyphenol isolated from tea, with cancer-preventive activities. In Vitro: The amount of (-)-Gallocatechin gallate does not differ in leaves of different stages, and the content is relatively low[1]. (−)-gallocatechin gallate in combination with active catechins ((−)-epigallocatechin gallate) has synergistic effects on the induction of apoptosis and inhibition of cell growth for […]

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(-)-Gallocatechin gallate 10mM/1mL  | ≥98%

MedChem Express

(-)-Gallocatechin gallate is the polyphenol isolated from tea, with cancer-preventive activities. In Vitro: The amount of (-)-Gallocatechin gallate does not differ in leaves of different stages, and the content is relatively low[1]. (−)-gallocatechin gallate in combination with active catechins ((−)-epigallocatechin gallate) has synergistic effects on the induction of apoptosis and inhibition of cell growth for […]

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(-)-Huperzine A 10mM/1mL  | ≥98%

MedChem Express

Huperzine A, an active Lycopodium alkaloid extracted from traditional Chinese herb, is a potent, selective and reversible acetylcholinesterase (AChE) inhibitor and has been widely used in China for the treatment of Alzheimer’s disease (AD). IC50 value: Target: AChE Huperzine A exhibited protective effects against d-gal-induced hepatotoxicity and inflamm-aging by inhibiting AChE activity and via the […]

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(-)-Huperzine A 5mg  | ≥98%

MedChem Express

Huperzine A, an active Lycopodium alkaloid extracted from traditional Chinese herb, is a potent, selective and reversible acetylcholinesterase (AChE) inhibitor and has been widely used in China for the treatment of Alzheimer’s disease (AD). IC50 value: Target: AChE Huperzine A exhibited protective effects against d-gal-induced hepatotoxicity and inflamm-aging by inhibiting AChE activity and via the […]

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(-)-Huperzine A 10mg  | ≥98%

MedChem Express

Huperzine A, an active Lycopodium alkaloid extracted from traditional Chinese herb, is a potent, selective and reversible acetylcholinesterase (AChE) inhibitor and has been widely used in China for the treatment of Alzheimer’s disease (AD). IC50 value: Target: AChE Huperzine A exhibited protective effects against d-gal-induced hepatotoxicity and inflamm-aging by inhibiting AChE activity and via the […]

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