Comparison

Molecules

1437732 Item(s)

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Name PDF Type Clone Specific against Appl. Host Item no. Amount Price
VP-­4604 Chemicals Other VP-4604 is a potent anti-methicillin-resistant Staphylococcus aureus (MRSA) agent. VP-4604 exhibits significant microbial growth inhibition toward Staphylococcus aureus (ATCC 43300) with MIC of 4-8 µg/mL. VP-4604 inhibits the growth of methicillin‐resista DCC-DC71474-100mg

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VP-­4604 Chemicals Other VP-4604 is a potent anti-methicillin-resistant Staphylococcus aureus (MRSA) agent. VP-4604 exhibits significant microbial growth inhibition toward Staphylococcus aureus (ATCC 43300) with MIC of 4-8 µg/mL. VP-4604 inhibits the growth of methicillin‐resista DCC-DC71474-250mg

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VP-­4604 Chemicals Other VP-4604 is a potent anti-methicillin-resistant Staphylococcus aureus (MRSA) agent. VP-4604 exhibits significant microbial growth inhibition toward Staphylococcus aureus (ATCC 43300) with MIC of 4-8 µg/mL. VP-4604 inhibits the growth of methicillin‐resista DCC-DC71474-1g

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Norastemizole Chemicals Other Tecastemizole (Norastemizole), a major metabolite of Astemizole, is a potent and selective H1 receptor antagonist. Tecastemizole shows anti-inflammatory activities. DCC-DC71335-100mg

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Norastemizole Chemicals Other Tecastemizole (Norastemizole), a major metabolite of Astemizole, is a potent and selective H1 receptor antagonist. Tecastemizole shows anti-inflammatory activities. DCC-DC71335-250mg

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Norastemizole Chemicals Other Tecastemizole (Norastemizole), a major metabolite of Astemizole, is a potent and selective H1 receptor antagonist. Tecastemizole shows anti-inflammatory activities. DCC-DC71335-1g

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LY-­3537982 Chemicals Other other, IV DCC-DC70578-100mg

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LY-­3537982 Chemicals Other other, IV DCC-DC70578-250mg

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LY-­3537982 Chemicals Other other, IV DCC-DC70578-1g

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YSK 05 Chemicals Other IV DCC-DC71417-100mg

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Branaplam hydrochloride Chemicals Other Branaplam (LMI070; NVS-SM1) hydrochloride is a highly potent, selective and orally active survival motor neuron-2 (SMN2) splicing modulator with an EC50 of 20 nM for SMN. Branaplam hydrochloride inhibits human-ether-a-go-go-related gene (hERG) with an IC50 of 6.3 μM. Branaplam hydrochloride elevates full-length SMN DCC-DC71300-100mg

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Branaplam hydrochloride Chemicals Other Branaplam (LMI070; NVS-SM1) hydrochloride is a highly potent, selective and orally active survival motor neuron-2 (SMN2) splicing modulator with an EC50 of 20 nM for SMN. Branaplam hydrochloride inhibits human-ether-a-go-go-related gene (hERG) with an IC50 of 6.3 μM. Branaplam hydrochloride elevates full-length SMN DCC-DC71300-250mg

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Branaplam hydrochloride Chemicals Other Branaplam (LMI070; NVS-SM1) hydrochloride is a highly potent, selective and orally active survival motor neuron-2 (SMN2) splicing modulator with an EC50 of 20 nM for SMN. Branaplam hydrochloride inhibits human-ether-a-go-go-related gene (hERG) with an IC50 of 6.3 μM. Branaplam hydrochloride elevates full-length SMN DCC-DC71300-1g

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CJ033466 Chemicals Other CJ033466 is a novel and selective 5-HT4 receptor partial agonist with an EC50 of 9 nM and has gastroprokinetic effect. DCC-DC71221-100mg

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CJ033466 Chemicals Other CJ033466 is a novel and selective 5-HT4 receptor partial agonist with an EC50 of 9 nM and has gastroprokinetic effect. DCC-DC71221-250mg

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CJ033466 Chemicals Other CJ033466 is a novel and selective 5-HT4 receptor partial agonist with an EC50 of 9 nM and has gastroprokinetic effect. DCC-DC71221-1g

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GSK329 Chemicals Other GSK329 is a potent and selective diarylurea inhibitor of the cardiac-specific kinase TNNI3K. GSK329 exhibits positive cardioprotective outcomes in the model of ischemia/reperfusion cardiac injury. DCC-DC71188-100mg

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GSK329 Chemicals Other GSK329 is a potent and selective diarylurea inhibitor of the cardiac-specific kinase TNNI3K. GSK329 exhibits positive cardioprotective outcomes in the model of ischemia/reperfusion cardiac injury. DCC-DC71188-250mg

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GSK329 Chemicals Other GSK329 is a potent and selective diarylurea inhibitor of the cardiac-specific kinase TNNI3K. GSK329 exhibits positive cardioprotective outcomes in the model of ischemia/reperfusion cardiac injury. DCC-DC71188-1g

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GRK6 inhibitor 18 Chemicals Other GRK6 inhibitor 18 is a potent, and selective GRK6 inhibitor with IC50 of 8 nM.GRK6 inhibitor 18 displays >1, 000-fold selectivity over Aurora A, as well as high selectivity against a panel of 85 kinases.GRK6 inhibitor 18 has potent cellular target engagement and antiproliferative activity against MM cells (IC50=0.4-0.46 uM) and is synergistic with bortezomib. DCC-DC70442-5mg

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MCI-­INI-­3 Chemicals Other other DCC-DC70590-5mg

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SR2640 hydrochloride Chemicals Other ELISA, other DCC-DC71156-100mg

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SR2640 hydrochloride Chemicals Other ELISA, other DCC-DC71156-250mg

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SR2640 hydrochloride Chemicals Other ELISA, other DCC-DC71156-1g

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Lysyllysyllysine Chemicals Other Lysyllysyllysine is a cationic moietie that may be used in the construction of gene delivery vectors and DNA nanoparticles. DCC-DC70000-1g

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Name Price
VP-­4604 Login
Type Chemicals
Clone
Specific against Other
Appl. VP-4604 is a potent anti-methicillin-resistant Staphylococcus aureus (MRSA) agent. VP-4604 exhibits significant microbial growth inhibition toward Staphylococcus aureus (ATCC 43300) with MIC of 4-8 µg/mL. VP-4604 inhibits the growth of methicillin‐resista
Host
Item no.
Amount 100 mg
Available
VP-­4604 Login
Type Chemicals
Clone
Specific against Other
Appl. VP-4604 is a potent anti-methicillin-resistant Staphylococcus aureus (MRSA) agent. VP-4604 exhibits significant microbial growth inhibition toward Staphylococcus aureus (ATCC 43300) with MIC of 4-8 µg/mL. VP-4604 inhibits the growth of methicillin‐resista
Host
Item no.
Amount 250 mg
Available
VP-­4604 Login
Type Chemicals
Clone
Specific against Other
Appl. VP-4604 is a potent anti-methicillin-resistant Staphylococcus aureus (MRSA) agent. VP-4604 exhibits significant microbial growth inhibition toward Staphylococcus aureus (ATCC 43300) with MIC of 4-8 µg/mL. VP-4604 inhibits the growth of methicillin‐resista
Host
Item no.
Amount 1 g
Available
Norastemizole Login
Type Chemicals
Clone
Specific against Other
Appl. Tecastemizole (Norastemizole), a major metabolite of Astemizole, is a potent and selective H1 receptor antagonist. Tecastemizole shows anti-inflammatory activities.
Host
Item no.
Amount 100 mg
Available
Norastemizole Login
Type Chemicals
Clone
Specific against Other
Appl. Tecastemizole (Norastemizole), a major metabolite of Astemizole, is a potent and selective H1 receptor antagonist. Tecastemizole shows anti-inflammatory activities.
Host
Item no.
Amount 250 mg
Available
Norastemizole Login
Type Chemicals
Clone
Specific against Other
Appl. Tecastemizole (Norastemizole), a major metabolite of Astemizole, is a potent and selective H1 receptor antagonist. Tecastemizole shows anti-inflammatory activities.
Host
Item no.
Amount 1 g
Available
LY-­3537982 Login
Type Chemicals
Clone
Specific against Other
Appl. other, IV
Host
Item no.
Amount 100 mg
Available
LY-­3537982 Login
Type Chemicals
Clone
Specific against Other
Appl. other, IV
Host
Item no.
Amount 250 mg
Available
LY-­3537982 Login
Type Chemicals
Clone
Specific against Other
Appl. other, IV
Host
Item no.
Amount 1 g
Available
YSK 05 Login
Type Chemicals
Clone
Specific against Other
Appl. IV
Host
Item no.
Amount 100 mg
Available
Branaplam hydrochloride Login
Type Chemicals
Clone
Specific against Other
Appl. Branaplam (LMI070; NVS-SM1) hydrochloride is a highly potent, selective and orally active survival motor neuron-2 (SMN2) splicing modulator with an EC50 of 20 nM for SMN. Branaplam hydrochloride inhibits human-ether-a-go-go-related gene (hERG) with an IC50 of 6.3 μM. Branaplam hydrochloride elevates full-length SMN
Host
Item no.
Amount 100 mg
Available
Branaplam hydrochloride Login
Type Chemicals
Clone
Specific against Other
Appl. Branaplam (LMI070; NVS-SM1) hydrochloride is a highly potent, selective and orally active survival motor neuron-2 (SMN2) splicing modulator with an EC50 of 20 nM for SMN. Branaplam hydrochloride inhibits human-ether-a-go-go-related gene (hERG) with an IC50 of 6.3 μM. Branaplam hydrochloride elevates full-length SMN
Host
Item no.
Amount 250 mg
Available
Branaplam hydrochloride Login
Type Chemicals
Clone
Specific against Other
Appl. Branaplam (LMI070; NVS-SM1) hydrochloride is a highly potent, selective and orally active survival motor neuron-2 (SMN2) splicing modulator with an EC50 of 20 nM for SMN. Branaplam hydrochloride inhibits human-ether-a-go-go-related gene (hERG) with an IC50 of 6.3 μM. Branaplam hydrochloride elevates full-length SMN
Host
Item no.
Amount 1 g
Available
CJ033466 Login
Type Chemicals
Clone
Specific against Other
Appl. CJ033466 is a novel and selective 5-HT4 receptor partial agonist with an EC50 of 9 nM and has gastroprokinetic effect.
Host
Item no.
Amount 100 mg
Available
CJ033466 Login
Type Chemicals
Clone
Specific against Other
Appl. CJ033466 is a novel and selective 5-HT4 receptor partial agonist with an EC50 of 9 nM and has gastroprokinetic effect.
Host
Item no.
Amount 250 mg
Available
CJ033466 Login
Type Chemicals
Clone
Specific against Other
Appl. CJ033466 is a novel and selective 5-HT4 receptor partial agonist with an EC50 of 9 nM and has gastroprokinetic effect.
Host
Item no.
Amount 1 g
Available
GSK329 Login
Type Chemicals
Clone
Specific against Other
Appl. GSK329 is a potent and selective diarylurea inhibitor of the cardiac-specific kinase TNNI3K. GSK329 exhibits positive cardioprotective outcomes in the model of ischemia/reperfusion cardiac injury.
Host
Item no.
Amount 100 mg
Available
GSK329 Login
Type Chemicals
Clone
Specific against Other
Appl. GSK329 is a potent and selective diarylurea inhibitor of the cardiac-specific kinase TNNI3K. GSK329 exhibits positive cardioprotective outcomes in the model of ischemia/reperfusion cardiac injury.
Host
Item no.
Amount 250 mg
Available
GSK329 Login
Type Chemicals
Clone
Specific against Other
Appl. GSK329 is a potent and selective diarylurea inhibitor of the cardiac-specific kinase TNNI3K. GSK329 exhibits positive cardioprotective outcomes in the model of ischemia/reperfusion cardiac injury.
Host
Item no.
Amount 1 g
Available
GRK6 inhibitor 18 Login
Type Chemicals
Clone
Specific against Other
Appl. GRK6 inhibitor 18 is a potent, and selective GRK6 inhibitor with IC50 of 8 nM.GRK6 inhibitor 18 displays >1, 000-fold selectivity over Aurora A, as well as high selectivity against a panel of 85 kinases.GRK6 inhibitor 18 has potent cellular target engagement and antiproliferative activity against MM cells (IC50=0.4-0.46 uM) and is synergistic with bortezomib.
Host
Item no.
Amount 5 mg
Available
MCI-­INI-­3 Login
Type Chemicals
Clone
Specific against Other
Appl. other
Host
Item no.
Amount 5 mg
Available
SR2640 hydrochloride Login
Type Chemicals
Clone
Specific against Other
Appl. ELISA, other
Host
Item no.
Amount 100 mg
Available
SR2640 hydrochloride Login
Type Chemicals
Clone
Specific against Other
Appl. ELISA, other
Host
Item no.
Amount 250 mg
Available
SR2640 hydrochloride Login
Type Chemicals
Clone
Specific against Other
Appl. ELISA, other
Host
Item no.
Amount 1 g
Available
Lysyllysyllysine Login
Type Chemicals
Clone
Specific against Other
Appl. Lysyllysyllysine is a cationic moietie that may be used in the construction of gene delivery vectors and DNA nanoparticles.
Host
Item no.
Amount 1 g
Available

1437732 Item(s)

per page