Comparison

Molecules

1437732 Item(s)

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Name PDF Type Clone Specific against Appl. Host Item no. Amount Price
DSPE-­PEG 2000 Chemicals Other PEG2000-DSPE is used for creating micelles that are able to carry drugs with low solubility. DCC-DC58047-1g

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GLPG2938 Chemicals Other GLPG2938 is an antagonists of sphingosine-​1-​phosphate (S1P) receptor for prophylaxis and​/or treatment of diseases including fibrotic, inflammatory, autoimmune, metabolic, cardiovascular, and​/or proliferative diseases. GLPG2938 displayed S1P inhibitory activity.with EC50 value of 9.5 nM (S1P2 antagonist EC50)​. DCC-DC57010-100mg

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GLPG2938 Chemicals Other GLPG2938 is an antagonists of sphingosine-​1-​phosphate (S1P) receptor for prophylaxis and​/or treatment of diseases including fibrotic, inflammatory, autoimmune, metabolic, cardiovascular, and​/or proliferative diseases. GLPG2938 displayed S1P inhibitory activity.with EC50 value of 9.5 nM (S1P2 antagonist EC50)​. DCC-DC57010-250mg

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GLPG2938 Chemicals Other GLPG2938 is an antagonists of sphingosine-​1-​phosphate (S1P) receptor for prophylaxis and​/or treatment of diseases including fibrotic, inflammatory, autoimmune, metabolic, cardiovascular, and​/or proliferative diseases. GLPG2938 displayed S1P inhibitory activity.with EC50 value of 9.5 nM (S1P2 antagonist EC50)​. DCC-DC57010-1g

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DDO-­5936 Chemicals Other IV DCC-DC57011-100mg

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DDO-­5936 Chemicals Other IV DCC-DC57011-250mg

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DDO-­5936 Chemicals Other IV DCC-DC57011-1g

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PF-­9363 Chemicals Other other DCC-DC57012-100mg

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PF-­9363 Chemicals Other other DCC-DC57012-250mg

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PF-­9363 Chemicals Other other DCC-DC57012-1g

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1,2-­DSPC Chemicals Other DCC-DC57005-1g

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Avatrombopag Chemicals Other ELISA, other DCC-DC57020-100mg

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Avatrombopag Chemicals Other ELISA, other DCC-DC57020-250mg

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Avatrombopag Chemicals Other ELISA, other DCC-DC57020-1g

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Rineterkib(ERK-­IN-­1;compound B) Chemicals Other Rineterkib, also known as LTT-462 or ERK-IN-1, is a RAF and ERK1/2 inhibitor which has demonstrated preclinical activity in multiple MAPK activated cancer cells and xenograft models. LTT462 binds to and inhibits ERK, thereby preventing the activation of ERK-mediated signal transduction pathways. This results in the inhibition of ERK-dependent tumor cell proliferation and survival. The mitogen-activated protein kinase (MAPK)/ERK pathway is upregulated in numerous tumor, differentiation and survival. DCC-DC57035-25mg

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UNC6934 Chemicals Other UNC6934 is a potent and selective drug-like chemical probe to interrogate the function of NSD2-PWWP1 with Kd of 91 nM.UNC6934 disrupts the NSD2-PWWP1 interaction with H3K36me2 nucleosomes in U2OS cells as measured by a NanoBret assay with an IC50 of 1.09 , a closely-related control compound, with an iso-propyl group replacing a cyclo-propyl group, is inactive by SPR and NanoBret assays. DCC-DC57111-100mg

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UNC6934 Chemicals Other a closely-related control compound, with an iso-propyl group replacing a cyclo-propyl group, is inactive by SPR and NanoBret assays., UNC6934 is a potent and selective drug-like chemical probe to interrogate the function of NSD2-PWWP1 with Kd of 91 nM.UNC6934 disrupts the NSD2-PWWP1 interaction with H3K36me2 nucleosomes in U2OS cells as measured by a NanoBret assay with an IC50 of 1.09 DCC-DC57111-250mg

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MRTX-­282 Chemicals Other MRTX-282 is a novel KRas G12D inhibitor. DCC-DC58042-5mg

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HG106 Chemicals Other HG106 is a potent SLC7A11 inhibitor and enhances ROS generation, ER stress, and ultimately growth arrest specifically in KRAS-mutant lung adenocarcinoma (LUAD). DCC-DC58063-10mg

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EUK-­134 Chemicals Other EUK-134 is an antioxidant compound with superoxide dismutase and catalase activity for oxidative species such as peroxynitrite, superoxide, and hydrogen peroxide. DCC-DC57040-100mg

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EUK-­134 Chemicals Other EUK-134 is an antioxidant compound with superoxide dismutase and catalase activity for oxidative species such as peroxynitrite, superoxide, and hydrogen peroxide. DCC-DC57040-250mg

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EUK-­134 Chemicals Other EUK-134 is an antioxidant compound with superoxide dismutase and catalase activity for oxidative species such as peroxynitrite, superoxide, and hydrogen peroxide. DCC-DC57040-1g

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N-­​Me-­​L-­​Ala-­​maytansinol Chemicals Other N-​Me-​L-​Ala-​maytansinol is a maytansine derivative. .N-​Me-​L-​Ala-​maytansinol can be used for synthesis of antibody-drug conjugate (ADC). DCC-DC57041-100mg

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DEOXYNIVALENOL Chemicals Other Deoxynivalenol, a mycotoxin of the trichothecenes family, crosses the intestinal mucosa by a paracellular pathway through the tight junctions. The Deoxynivalenol transport is not affected by P-glycoprotein (PgP) or multidrug resistance-associated proteins (MRPs) inhibitors[1]. DCC-DC57042-5mg

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AEOL-­10150 (pentachloride) Chemicals Other AEOL-10150 pentachloride is a metalloporphyrin catalytic antioxidant and is a superoxide dismutase mimetic, and protects lungs from radiation-induced injury[1]. DCC-DC59006-100mg

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Name Price
DSPE-­PEG 2000 Login
Type Chemicals
Clone
Specific against Other
Appl. PEG2000-DSPE is used for creating micelles that are able to carry drugs with low solubility.
Host
Item no.
Amount 1 g
Available
GLPG2938 Login
Type Chemicals
Clone
Specific against Other
Appl. GLPG2938 is an antagonists of sphingosine-​1-​phosphate (S1P) receptor for prophylaxis and​/or treatment of diseases including fibrotic, inflammatory, autoimmune, metabolic, cardiovascular, and​/or proliferative diseases. GLPG2938 displayed S1P inhibitory activity.with EC50 value of 9.5 nM (S1P2 antagonist EC50)​.
Host
Item no.
Amount 100 mg
Available
GLPG2938 Login
Type Chemicals
Clone
Specific against Other
Appl. GLPG2938 is an antagonists of sphingosine-​1-​phosphate (S1P) receptor for prophylaxis and​/or treatment of diseases including fibrotic, inflammatory, autoimmune, metabolic, cardiovascular, and​/or proliferative diseases. GLPG2938 displayed S1P inhibitory activity.with EC50 value of 9.5 nM (S1P2 antagonist EC50)​.
Host
Item no.
Amount 250 mg
Available
GLPG2938 Login
Type Chemicals
Clone
Specific against Other
Appl. GLPG2938 is an antagonists of sphingosine-​1-​phosphate (S1P) receptor for prophylaxis and​/or treatment of diseases including fibrotic, inflammatory, autoimmune, metabolic, cardiovascular, and​/or proliferative diseases. GLPG2938 displayed S1P inhibitory activity.with EC50 value of 9.5 nM (S1P2 antagonist EC50)​.
Host
Item no.
Amount 1 g
Available
DDO-­5936 Login
Type Chemicals
Clone
Specific against Other
Appl. IV
Host
Item no.
Amount 100 mg
Available
DDO-­5936 Login
Type Chemicals
Clone
Specific against Other
Appl. IV
Host
Item no.
Amount 250 mg
Available
DDO-­5936 Login
Type Chemicals
Clone
Specific against Other
Appl. IV
Host
Item no.
Amount 1 g
Available
PF-­9363 Login
Type Chemicals
Clone
Specific against Other
Appl. other
Host
Item no.
Amount 100 mg
Available
PF-­9363 Login
Type Chemicals
Clone
Specific against Other
Appl. other
Host
Item no.
Amount 250 mg
Available
PF-­9363 Login
Type Chemicals
Clone
Specific against Other
Appl. other
Host
Item no.
Amount 1 g
Available
1,2-­DSPC Login
Type Chemicals
Clone
Specific against Other
Appl.
Host
Item no.
Amount 1 g
Available
Avatrombopag Login
Type Chemicals
Clone
Specific against Other
Appl. ELISA, other
Host
Item no.
Amount 100 mg
Available
Avatrombopag Login
Type Chemicals
Clone
Specific against Other
Appl. ELISA, other
Host
Item no.
Amount 250 mg
Available
Avatrombopag Login
Type Chemicals
Clone
Specific against Other
Appl. ELISA, other
Host
Item no.
Amount 1 g
Available
Rineterkib(ERK-­IN-­1;compound B) Login
Type Chemicals
Clone
Specific against Other
Appl. Rineterkib, also known as LTT-462 or ERK-IN-1, is a RAF and ERK1/2 inhibitor which has demonstrated preclinical activity in multiple MAPK activated cancer cells and xenograft models. LTT462 binds to and inhibits ERK, thereby preventing the activation of ERK-mediated signal transduction pathways. This results in the inhibition of ERK-dependent tumor cell proliferation and survival. The mitogen-activated protein kinase (MAPK)/ERK pathway is upregulated in numerous tumor, differentiation and survival.
Host
Item no.
Amount 25 mg
Available
UNC6934 Login
Type Chemicals
Clone
Specific against Other
Appl. UNC6934 is a potent and selective drug-like chemical probe to interrogate the function of NSD2-PWWP1 with Kd of 91 nM.UNC6934 disrupts the NSD2-PWWP1 interaction with H3K36me2 nucleosomes in U2OS cells as measured by a NanoBret assay with an IC50 of 1.09 , a closely-related control compound, with an iso-propyl group replacing a cyclo-propyl group, is inactive by SPR and NanoBret assays.
Host
Item no.
Amount 100 mg
Available
UNC6934 Login
Type Chemicals
Clone
Specific against Other
Appl. a closely-related control compound, with an iso-propyl group replacing a cyclo-propyl group, is inactive by SPR and NanoBret assays., UNC6934 is a potent and selective drug-like chemical probe to interrogate the function of NSD2-PWWP1 with Kd of 91 nM.UNC6934 disrupts the NSD2-PWWP1 interaction with H3K36me2 nucleosomes in U2OS cells as measured by a NanoBret assay with an IC50 of 1.09
Host
Item no.
Amount 250 mg
Available
MRTX-­282 Login
Type Chemicals
Clone
Specific against Other
Appl. MRTX-282 is a novel KRas G12D inhibitor.
Host
Item no.
Amount 5 mg
Available
HG106 Login
Type Chemicals
Clone
Specific against Other
Appl. HG106 is a potent SLC7A11 inhibitor and enhances ROS generation, ER stress, and ultimately growth arrest specifically in KRAS-mutant lung adenocarcinoma (LUAD).
Host
Item no.
Amount 10 mg
Available
EUK-­134 Login
Type Chemicals
Clone
Specific against Other
Appl. EUK-134 is an antioxidant compound with superoxide dismutase and catalase activity for oxidative species such as peroxynitrite, superoxide, and hydrogen peroxide.
Host
Item no.
Amount 100 mg
Available
EUK-­134 Login
Type Chemicals
Clone
Specific against Other
Appl. EUK-134 is an antioxidant compound with superoxide dismutase and catalase activity for oxidative species such as peroxynitrite, superoxide, and hydrogen peroxide.
Host
Item no.
Amount 250 mg
Available
EUK-­134 Login
Type Chemicals
Clone
Specific against Other
Appl. EUK-134 is an antioxidant compound with superoxide dismutase and catalase activity for oxidative species such as peroxynitrite, superoxide, and hydrogen peroxide.
Host
Item no.
Amount 1 g
Available
N-­​Me-­​L-­​Ala-­​maytansinol Login
Type Chemicals
Clone
Specific against Other
Appl. N-​Me-​L-​Ala-​maytansinol is a maytansine derivative. .N-​Me-​L-​Ala-​maytansinol can be used for synthesis of antibody-drug conjugate (ADC).
Host
Item no.
Amount 100 mg
Available
DEOXYNIVALENOL Login
Type Chemicals
Clone
Specific against Other
Appl. Deoxynivalenol, a mycotoxin of the trichothecenes family, crosses the intestinal mucosa by a paracellular pathway through the tight junctions. The Deoxynivalenol transport is not affected by P-glycoprotein (PgP) or multidrug resistance-associated proteins (MRPs) inhibitors[1].
Host
Item no.
Amount 5 mg
Available
AEOL-­10150 (pentachloride) Login
Type Chemicals
Clone
Specific against Other
Appl. AEOL-10150 pentachloride is a metalloporphyrin catalytic antioxidant and is a superoxide dismutase mimetic, and protects lungs from radiation-induced injury[1].
Host
Item no.
Amount 100 mg
Available

1437732 Item(s)

per page