MedChem Express

MedChem Express logo

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.

Company Website

Product Listing

VAL-083 5mg  | ≥98%

MedChem Express

VAL-083 is an alkylating agent that creates N7 methylation on DNA, with antitumor activity. IC50 & Target: DNA Alkylator[1] In Vitro: VAL-083 is an alkylating agent that creates N7 methylation on DNA. VAL-083 suppresses U251 and SF188 cell growth and induces apoptosis after 72 h. VAL-083 (5 μM) inhibits the growth of SF188 by ∼95%. […]

More Information Supplier Page

VAL-083 10mg  | ≥98%

MedChem Express

VAL-083 is an alkylating agent that creates N7 methylation on DNA, with antitumor activity. IC50 & Target: DNA Alkylator[1] In Vitro: VAL-083 is an alkylating agent that creates N7 methylation on DNA. VAL-083 suppresses U251 and SF188 cell growth and induces apoptosis after 72 h. VAL-083 (5 μM) inhibits the growth of SF188 by ∼95%. […]

More Information Supplier Page

VAL-083 50mg  | ≥98%

MedChem Express

VAL-083 is an alkylating agent that creates N7 methylation on DNA, with antitumor activity. IC50 & Target: DNA Alkylator[1] In Vitro: VAL-083 is an alkylating agent that creates N7 methylation on DNA. VAL-083 suppresses U251 and SF188 cell growth and induces apoptosis after 72 h. VAL-083 (5 μM) inhibits the growth of SF188 by ∼95%. […]

More Information Supplier Page

Val-Cit-PAB-MMAE 1mg  | ≥98%

MedChem Express

Val-Cit-PAB-MMAE is a drug-linker conjugate for ADC by using the anti-mitotic agent, monomethyl auristatin E (MMAE), linked via the peptide Val-Cit-PAB.

More Information Supplier Page

Val-Cit-PAB-MMAE 10mg  | ≥98%

MedChem Express

Val-Cit-PAB-MMAE is a drug-linker conjugate for ADC by using the anti-mitotic agent, monomethyl auristatin E (MMAE), linked via the peptide Val-Cit-PAB.

More Information Supplier Page

Val-Cit-PAB-MMAE 5mg  | ≥98%

MedChem Express

Val-Cit-PAB-MMAE is a drug-linker conjugate for ADC by using the anti-mitotic agent, monomethyl auristatin E (MMAE), linked via the peptide Val-Cit-PAB.

More Information Supplier Page

Val-Cit-PAB-MMAE 10mM/1mL  | ≥98%

MedChem Express

Val-Cit-PAB-MMAE is a drug-linker conjugate for ADC by using the anti-mitotic agent, monomethyl auristatin E (MMAE), linked via the peptide Val-Cit-PAB.

More Information Supplier Page

Valacyclovir 10mg  | ≥98%

MedChem Express

Valacyclovir is an antiviral drug used in the management of herpes simplex, herpes zoster, and herpes B. IC50 Value: 2.9 microg/ml (for HSV-1 W)[4]. Target: HSV infection in vitro: VACV uptake was concentration dependent and saturable with a Michaelis-Menten constant and maximum velocity of 1.64 +/- 0.06 mM and 23.34 +/- 0.36 nmol/mg protein/5 min, […]

More Information Supplier Page

Valacyclovir 50mg  | ≥98%

MedChem Express

Valacyclovir is an antiviral drug used in the management of herpes simplex, herpes zoster, and herpes B. IC50 Value: 2.9 microg/ml (for HSV-1 W)[4]. Target: HSV infection in vitro: VACV uptake was concentration dependent and saturable with a Michaelis-Menten constant and maximum velocity of 1.64 +/- 0.06 mM and 23.34 +/- 0.36 nmol/mg protein/5 min, […]

More Information Supplier Page

Valacyclovir (hydrochloride) 50mg  | ≥98%

MedChem Express

Valacyclovir hydrochloride is an antiviral drug used in the management of herpes simplex, herpes zoster, and herpes B. Target: HSV Valacyclovir is an antiviral drug used in the management of herpes simplex, herpes zoster, and herpes B. VACV uptake was concentration dependent and saturable with a Michaelis-Menten constant and maximum velocity of 1.64 +/- 0.06 […]

More Information Supplier Page

Valacyclovir (hydrochloride) 10mg  | ≥98%

MedChem Express

Valacyclovir hydrochloride is an antiviral drug used in the management of herpes simplex, herpes zoster, and herpes B. Target: HSV Valacyclovir is an antiviral drug used in the management of herpes simplex, herpes zoster, and herpes B. VACV uptake was concentration dependent and saturable with a Michaelis-Menten constant and maximum velocity of 1.64 +/- 0.06 […]

More Information Supplier Page

Valacyclovir (hydrochloride) 10mM/1mL  | ≥98%

MedChem Express

Valacyclovir hydrochloride is an antiviral drug used in the management of herpes simplex, herpes zoster, and herpes B. Target: HSV Valacyclovir is an antiviral drug used in the management of herpes simplex, herpes zoster, and herpes B. VACV uptake was concentration dependent and saturable with a Michaelis-Menten constant and maximum velocity of 1.64 +/- 0.06 […]

More Information Supplier Page

Valbenazine 10mM/1mL  | ≥98%

MedChem Express

Valbenazine is a prodrug of the (+)-α isomer of tetrabenazine for tardive syndrome therapy, and inhibits VMAT2 function. In Vivo: Valbenazine shows a distinctive improvement in tardive dyskinesia symptoms during the successful Phase II trial[1].

More Information Supplier Page

Valbenazine 50mg  | ≥98%

MedChem Express

Valbenazine is a prodrug of the (+)-α isomer of tetrabenazine for tardive syndrome therapy, and inhibits VMAT2 function. In Vivo: Valbenazine shows a distinctive improvement in tardive dyskinesia symptoms during the successful Phase II trial[1].

More Information Supplier Page

Valbenazine 2mg  | ≥98%

MedChem Express

Valbenazine is a prodrug of the (+)-α isomer of tetrabenazine for tardive syndrome therapy, and inhibits VMAT2 function. In Vivo: Valbenazine shows a distinctive improvement in tardive dyskinesia symptoms during the successful Phase II trial[1].

More Information Supplier Page

Valbenazine 5mg  | ≥98%

MedChem Express

Valbenazine is a prodrug of the (+)-α isomer of tetrabenazine for tardive syndrome therapy, and inhibits VMAT2 function. In Vivo: Valbenazine shows a distinctive improvement in tardive dyskinesia symptoms during the successful Phase II trial[1].

More Information Supplier Page

Valbenazine 10mg  | ≥98%

MedChem Express

Valbenazine is a prodrug of the (+)-α isomer of tetrabenazine for tardive syndrome therapy, and inhibits VMAT2 function. In Vivo: Valbenazine shows a distinctive improvement in tardive dyskinesia symptoms during the successful Phase II trial[1].

More Information Supplier Page

Valbenazine 25mg  | ≥98%

MedChem Express

Valbenazine is a prodrug of the (+)-α isomer of tetrabenazine for tardive syndrome therapy, and inhibits VMAT2 function. In Vivo: Valbenazine shows a distinctive improvement in tardive dyskinesia symptoms during the successful Phase II trial[1].

More Information Supplier Page

Valbenazine 100mg  | ≥98%

MedChem Express

Valbenazine is a prodrug of the (+)-α isomer of tetrabenazine for tardive syndrome therapy, and inhibits VMAT2 function. In Vivo: Valbenazine shows a distinctive improvement in tardive dyskinesia symptoms during the successful Phase II trial[1].

More Information Supplier Page

Valdecoxib 50mg  | ≥98%

MedChem Express

Valdecoxib (SC 65872) is a COX-2 selective inhibitor with an IC50 value of 5 nM. IC50 Value: 5 nM (COX-2) [1] Target: COX-2 Valdecoxib is a non-steroidal anti-inflammatory drug (NSAID) used in the treatment of osteoarthritis, rheumatoid arthritis, and painful menstruation and menstrual symptoms. in vitro: The overall saturation binding affinity for COX-2 of valdecoxib […]

More Information Supplier Page

Valdecoxib 10mg  | ≥98%

MedChem Express

Valdecoxib (SC 65872) is a COX-2 selective inhibitor with an IC50 value of 5 nM. IC50 Value: 5 nM (COX-2) [1] Target: COX-2 Valdecoxib is a non-steroidal anti-inflammatory drug (NSAID) used in the treatment of osteoarthritis, rheumatoid arthritis, and painful menstruation and menstrual symptoms. in vitro: The overall saturation binding affinity for COX-2 of valdecoxib […]

More Information Supplier Page

Valdecoxib 10mM/1mL  | ≥98%

MedChem Express

Valdecoxib (SC 65872) is a COX-2 selective inhibitor with an IC50 value of 5 nM. IC50 Value: 5 nM (COX-2) [1] Target: COX-2 Valdecoxib is a non-steroidal anti-inflammatory drug (NSAID) used in the treatment of osteoarthritis, rheumatoid arthritis, and painful menstruation and menstrual symptoms. in vitro: The overall saturation binding affinity for COX-2 of valdecoxib […]

More Information Supplier Page

Valganciclovir 50mg  | ≥98%

MedChem Express

Valganciclovir, the L-valyl ester of ganciclovir, is actually a prodrug for ganciclovir. Valganciclovir is an antiviral medication used to treat cytomegalovirus infections. IC50 Value: Target: CMV in vitro: In cell culture model systems using Caco-2 cells for PEPT1 and SKPT cells for PEPT2, valganciclovir inhibited glycylsarcosine transport mediated by PEPT1 and PEPT2 with K(i) values […]

More Information Supplier Page

Valganciclovir 100mg  | ≥98%

MedChem Express

Valganciclovir, the L-valyl ester of ganciclovir, is actually a prodrug for ganciclovir. Valganciclovir is an antiviral medication used to treat cytomegalovirus infections. IC50 Value: Target: CMV in vitro: In cell culture model systems using Caco-2 cells for PEPT1 and SKPT cells for PEPT2, valganciclovir inhibited glycylsarcosine transport mediated by PEPT1 and PEPT2 with K(i) values […]

More Information Supplier Page

Valganciclovir (hydrochloride) 100mg  | ≥98%

MedChem Express

Valganciclovir (hydrochloride), the L-valyl ester of ganciclovir, is actually a prodrug for ganciclovir. Valganciclovir is an antiviral medication used to treat cytomegalovirus infections. IC50 Value: Target: CMV in vitro: In cell culture model systems using Caco-2 cells for PEPT1 and SKPT cells for PEPT2, valganciclovir inhibited glycylsarcosine transport mediated by PEPT1 and PEPT2 with K(i) […]

More Information Supplier Page

Valganciclovir (hydrochloride) 50mg  | ≥98%

MedChem Express

Valganciclovir (hydrochloride), the L-valyl ester of ganciclovir, is actually a prodrug for ganciclovir. Valganciclovir is an antiviral medication used to treat cytomegalovirus infections. IC50 Value: Target: CMV in vitro: In cell culture model systems using Caco-2 cells for PEPT1 and SKPT cells for PEPT2, valganciclovir inhibited glycylsarcosine transport mediated by PEPT1 and PEPT2 with K(i) […]

More Information Supplier Page

Valganciclovir (hydrochloride) 10mM/1mL  | ≥98%

MedChem Express

Valganciclovir (hydrochloride), the L-valyl ester of ganciclovir, is actually a prodrug for ganciclovir. Valganciclovir is an antiviral medication used to treat cytomegalovirus infections. IC50 Value: Target: CMV in vitro: In cell culture model systems using Caco-2 cells for PEPT1 and SKPT cells for PEPT2, valganciclovir inhibited glycylsarcosine transport mediated by PEPT1 and PEPT2 with K(i) […]

More Information Supplier Page

Valifenalate 1g  | ≥98%

MedChem Express

Valifenalate(IR5885; Valiphenal), which is approved for application on high-value crops such as grapes, tomatoes and other vegetables, is effective against various types of mildew and is currently marketed primarily under the Valis moniker; insecticide agent.

More Information Supplier Page

Valifenalate 5g  | ≥98%

MedChem Express

Valifenalate(IR5885; Valiphenal), which is approved for application on high-value crops such as grapes, tomatoes and other vegetables, is effective against various types of mildew and is currently marketed primarily under the Valis moniker; insecticide agent.

More Information Supplier Page

Valifenalate 10mM/1mL  | ≥98%

MedChem Express

Valifenalate(IR5885; Valiphenal), which is approved for application on high-value crops such as grapes, tomatoes and other vegetables, is effective against various types of mildew and is currently marketed primarily under the Valis moniker; insecticide agent.

More Information Supplier Page

Valorphin 25mg  | ≥98%

MedChem Express

Valorphin is an endogenous hemoglobin β-chain (33-39) fragment with opioid analgesic activity, binds to rat mu-opioid receptor, with an IC50 of 14 nM; Valorphin also shows anti-tumor activity. IC50 & Target: IC50: 14 nM (mu-opioid receptor), 200 nM (δ-opioid receptor)[1] In Vitro: Valorphin is a derivative of dihydrovaltrate with opioid analgesic activity, binds to rat […]

More Information Supplier Page

Valorphin 5mg  | ≥98%

MedChem Express

Valorphin is an endogenous hemoglobin β-chain (33-39) fragment with opioid analgesic activity, binds to rat mu-opioid receptor, with an IC50 of 14 nM; Valorphin also shows anti-tumor activity. IC50 & Target: IC50: 14 nM (mu-opioid receptor), 200 nM (δ-opioid receptor)[1] In Vitro: Valorphin is a derivative of dihydrovaltrate with opioid analgesic activity, binds to rat […]

More Information Supplier Page

Valorphin 10mg  | ≥98%

MedChem Express

Valorphin is an endogenous hemoglobin β-chain (33-39) fragment with opioid analgesic activity, binds to rat mu-opioid receptor, with an IC50 of 14 nM; Valorphin also shows anti-tumor activity. IC50 & Target: IC50: 14 nM (mu-opioid receptor), 200 nM (δ-opioid receptor)[1] In Vitro: Valorphin is a derivative of dihydrovaltrate with opioid analgesic activity, binds to rat […]

More Information Supplier Page

Valproic acid 10mM/1mL  | ≥98%

MedChem Express

Valproic acid is an HDAC inhibitor, with IC50 in the range of 0.5 and 2 mM, also inhibits HDAC1 (IC50, 400 μM), and induces proteasomal degradation of HDAC2; Valproic acid sodium salt is used in the treatment of epilepsy, bipolar disorder and prevention of migraine headaches. IC50 & Target: IC50: 400 μM (HDAC1), 0.5-2 mM […]

More Information Supplier Page

Valproic acid 5g  | ≥98%

MedChem Express

Valproic acid is an HDAC inhibitor, with IC50 in the range of 0.5 and 2 mM, also inhibits HDAC1 (IC50, 400 μM), and induces proteasomal degradation of HDAC2; Valproic acid sodium salt is used in the treatment of epilepsy, bipolar disorder and prevention of migraine headaches. IC50 & Target: IC50: 400 μM (HDAC1), 0.5-2 mM […]

More Information Supplier Page

Valproic acid 1g  | ≥98%

MedChem Express

Valproic acid is an HDAC inhibitor, with IC50 in the range of 0.5 and 2 mM, also inhibits HDAC1 (IC50, 400 μM), and induces proteasomal degradation of HDAC2; Valproic acid sodium salt is used in the treatment of epilepsy, bipolar disorder and prevention of migraine headaches. IC50 & Target: IC50: 400 μM (HDAC1), 0.5-2 mM […]

More Information Supplier Page

Valproic acid (sodium salt) 10mM/1mL  | ≥98%

MedChem Express

Valproic acid sodium salt is an HDAC inhibitor, with IC50 in the range of 0.5 and 2 mM, also inhibits HDAC1 (IC50, 400 μM), and induces proteasomal degradation of HDAC2; Valproic acid sodium salt is used in the treatment of epilepsy, bipolar disorder and prevention of migraine headaches. IC50 & Target: IC50: 400 μM (HDAC1), […]

More Information Supplier Page

Valproic acid (sodium salt) 1g  | ≥98%

MedChem Express

Valproic acid sodium salt is an HDAC inhibitor, with IC50 in the range of 0.5 and 2 mM, also inhibits HDAC1 (IC50, 400 μM), and induces proteasomal degradation of HDAC2; Valproic acid sodium salt is used in the treatment of epilepsy, bipolar disorder and prevention of migraine headaches. IC50 & Target: IC50: 400 μM (HDAC1), […]

More Information Supplier Page

Valproic acid (sodium salt) 5g  | ≥98%

MedChem Express

Valproic acid sodium salt is an HDAC inhibitor, with IC50 in the range of 0.5 and 2 mM, also inhibits HDAC1 (IC50, 400 μM), and induces proteasomal degradation of HDAC2; Valproic acid sodium salt is used in the treatment of epilepsy, bipolar disorder and prevention of migraine headaches. IC50 & Target: IC50: 400 μM (HDAC1), […]

More Information Supplier Page

Valpromide 10mM/1mL  | ≥98%

MedChem Express

Valpromide is an amide derivative of valproic acid and inhibits human epoxide hydrolase. IC50 & Target: epoxide hydrolase[1]

More Information Supplier Page

Valpromide 10mg  | ≥98%

MedChem Express

Valpromide is an amide derivative of valproic acid and inhibits human epoxide hydrolase. IC50 & Target: epoxide hydrolase[1]

More Information Supplier Page

Valpromide 50mg  | ≥98%

MedChem Express

Valpromide is an amide derivative of valproic acid and inhibits human epoxide hydrolase. IC50 & Target: epoxide hydrolase[1]

More Information Supplier Page