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1437732 Item(s)

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  2. 39
  3. 40
  4. 41
  5. 42
Name PDF Type Clone Specific against Appl. Host Item no. Amount ✓ Price
JH-­X-­119-­01 Chemicals Other Jh-X-119-01 is a novel potent and selective interleukin-1 receptor-associated kinases 1 (IRAK1) inhibitor. JH-X-119-01 irreversibly labels IRAK1 at C302. This compound exhibited cytotoxic activity at single digit micromolar concentrations in a panel of WM, DLBCL, and lymphoma cell lines expressing MYD88. Cotreatment of JH-X-119-01 with the BTK inhibitor ibrutinib resulted in synergistic killing effects in these systems. DCC-DC60125-1g

DCChemicals 		1 g Login
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ML303 Chemicals Other IC DCC-DC60130-100mg

DCChemicals 		100 mg Login
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ML303 Chemicals Other IC DCC-DC60130-250mg

DCChemicals 		250 mg Login
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ML303 Chemicals Other IC DCC-DC60130-1g

DCChemicals 		1 g Login
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SAR405 R enantiomer Chemicals Other SAR405 R enantiomer is the less active enantiomer of SAR405. SAR405 is an inhibitor of PIK3C3/Vps34. DCC-DC60133-100mg

DCChemicals 		100 mg Login
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SAR405 R enantiomer Chemicals Other SAR405 R enantiomer is the less active enantiomer of SAR405. SAR405 is an inhibitor of PIK3C3/Vps34. DCC-DC60133-250mg

DCChemicals 		250 mg Login
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SAR405 R enantiomer Chemicals Other SAR405 R enantiomer is the less active enantiomer of SAR405. SAR405 is an inhibitor of PIK3C3/Vps34. DCC-DC60133-1g

DCChemicals 		1 g Login
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Soporidine Chemicals Other Soporidine is a strigolactone (SL) antagonist and inhibitor of germination in their biological assays. It binds AtHTL and specifically interferes with SL signaling. DCC-DC60134-100mg

DCChemicals 		100 mg Login
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Soporidine Chemicals Other Soporidine is a strigolactone (SL) antagonist and inhibitor of germination in their biological assays. It binds AtHTL and specifically interferes with SL signaling. DCC-DC60134-250mg

DCChemicals 		250 mg Login
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Soporidine Chemicals Other Soporidine is a strigolactone (SL) antagonist and inhibitor of germination in their biological assays. It binds AtHTL and specifically interferes with SL signaling. DCC-DC60134-1g

DCChemicals 		1 g Login
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MT 63-­78 Chemicals Other MT 63-78 is a specific and effective direct AMPK activator (EC50: 25 μM). MT 63-78 blocks prostate cancer growth by inhibiting the lipogenesis and mTORC1 pathways. MT 63-78 has antitumor effects. MT 63–78 also causes cell mitotic arrest and apoptosis. DCC-DC60143-100mg

DCChemicals 		100 mg Login
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MT 63-­78 Chemicals Other MT 63-78 is a specific and effective direct AMPK activator (EC50: 25 μM). MT 63-78 blocks prostate cancer growth by inhibiting the lipogenesis and mTORC1 pathways. MT 63-78 has antitumor effects. MT 63–78 also causes cell mitotic arrest and apoptosis. DCC-DC60143-250mg

DCChemicals 		250 mg Login
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MT 63-­78 Chemicals Other MT 63-78 is a specific and effective direct AMPK activator (EC50: 25 μM). MT 63-78 blocks prostate cancer growth by inhibiting the lipogenesis and mTORC1 pathways. MT 63-78 has antitumor effects. MT 63–78 also causes cell mitotic arrest and apoptosis. DCC-DC60143-1g

DCChemicals 		1 g Login
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Lu AF27139 Chemicals Other IV DCC-DC60155-100mg

DCChemicals 		100 mg Login
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Lu AF27139 Chemicals Other IV DCC-DC60155-250mg

DCChemicals 		250 mg Login
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Lu AF27139 Chemicals Other IV DCC-DC60155-1g

DCChemicals 		1 g Login
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Rasarfin Chemicals Other other DCC-DC60156-100mg

DCChemicals 		100 mg Login
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Rasarfin Chemicals Other other DCC-DC60156-250mg

DCChemicals 		250 mg Login
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Rasarfin Chemicals Other other DCC-DC60156-1g

DCChemicals 		1 g Login
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K-­975 Chemicals Other K-975 is a first-in-class TEAD inhibitor, directly inhibiting YAP/TAZ-TEAD protein-protein interaction and showing a potent anti-tumor effect in malignant pleural mesothelioma. K-975 was covalently bound to an internal cysteine residue located in the palmitate-binding pocket of TEAD. K-975 had a DCC-DC60158-100mg

DCChemicals 		100 mg Login
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K-­975 Chemicals Other K-975 is a first-in-class TEAD inhibitor, directly inhibiting YAP/TAZ-TEAD protein-protein interaction and showing a potent anti-tumor effect in malignant pleural mesothelioma. K-975 was covalently bound to an internal cysteine residue located in the palmitate-binding pocket of TEAD. K-975 had a DCC-DC60158-250mg

DCChemicals 		250 mg Login
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K-­975 Chemicals Other K-975 is a first-in-class TEAD inhibitor, directly inhibiting YAP/TAZ-TEAD protein-protein interaction and showing a potent anti-tumor effect in malignant pleural mesothelioma. K-975 was covalently bound to an internal cysteine residue located in the palmitate-binding pocket of TEAD. K-975 had a DCC-DC60158-1g

DCChemicals 		1 g Login
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GPR52-­IN-­43(CAY10786) Chemicals Other GPR52-IN-43(CAY10786) is a novel GPR52 antagonist, reducing mHTT levels by targeting GPR52 and promoting survival of mouse primary striatal neurons, and also reducing HD-related phenotypes in HdhQ140. DCC-DC60162-100mg

DCChemicals 		100 mg Login
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GPR52-­IN-­43(CAY10786) Chemicals Other GPR52-IN-43(CAY10786) is a novel GPR52 antagonist, reducing mHTT levels by targeting GPR52 and promoting survival of mouse primary striatal neurons, and also reducing HD-related phenotypes in HdhQ140. DCC-DC60162-250mg

DCChemicals 		250 mg Login
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GPR52-­IN-­43(CAY10786) Chemicals Other GPR52-IN-43(CAY10786) is a novel GPR52 antagonist, reducing mHTT levels by targeting GPR52 and promoting survival of mouse primary striatal neurons, and also reducing HD-related phenotypes in HdhQ140. DCC-DC60162-1g

DCChemicals 		1 g Login
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Name Price
JH-­X-­119-­01 Login JH-X-119-01
Type Chemicals
Clone
Specific against Other
Appl. Jh-X-119-01 is a novel potent and selective interleukin-1 receptor-associated kinases 1 (IRAK1) inhibitor. JH-X-119-01 irreversibly labels IRAK1 at C302. This compound exhibited cytotoxic activity at single digit micromolar concentrations in a panel of WM, DLBCL, and lymphoma cell lines expressing MYD88. Cotreatment of JH-X-119-01 with the BTK inhibitor ibrutinib resulted in synergistic killing effects in these systems.
Host
Item no.
Amount 1 g
Available
ML303 Login ML303
Type Chemicals
Clone
Specific against Other
Appl. IC
Host
Item no.
Amount 100 mg
Available
ML303 Login ML303
Type Chemicals
Clone
Specific against Other
Appl. IC
Host
Item no.
Amount 250 mg
Available
ML303 Login ML303
Type Chemicals
Clone
Specific against Other
Appl. IC
Host
Item no.
Amount 1 g
Available
SAR405 R enantiomer Login SAR405 R enantiomer
Type Chemicals
Clone
Specific against Other
Appl. SAR405 R enantiomer is the less active enantiomer of SAR405. SAR405 is an inhibitor of PIK3C3/Vps34.
Host
Item no.
Amount 100 mg
Available
SAR405 R enantiomer Login SAR405 R enantiomer
Type Chemicals
Clone
Specific against Other
Appl. SAR405 R enantiomer is the less active enantiomer of SAR405. SAR405 is an inhibitor of PIK3C3/Vps34.
Host
Item no.
Amount 250 mg
Available
SAR405 R enantiomer Login SAR405 R enantiomer
Type Chemicals
Clone
Specific against Other
Appl. SAR405 R enantiomer is the less active enantiomer of SAR405. SAR405 is an inhibitor of PIK3C3/Vps34.
Host
Item no.
Amount 1 g
Available
Soporidine Login Soporidine
Type Chemicals
Clone
Specific against Other
Appl. Soporidine is a strigolactone (SL) antagonist and inhibitor of germination in their biological assays. It binds AtHTL and specifically interferes with SL signaling.
Host
Item no.
Amount 100 mg
Available
Soporidine Login Soporidine
Type Chemicals
Clone
Specific against Other
Appl. Soporidine is a strigolactone (SL) antagonist and inhibitor of germination in their biological assays. It binds AtHTL and specifically interferes with SL signaling.
Host
Item no.
Amount 250 mg
Available
Soporidine Login Soporidine
Type Chemicals
Clone
Specific against Other
Appl. Soporidine is a strigolactone (SL) antagonist and inhibitor of germination in their biological assays. It binds AtHTL and specifically interferes with SL signaling.
Host
Item no.
Amount 1 g
Available
MT 63-­78 Login MT 63-78
Type Chemicals
Clone
Specific against Other
Appl. MT 63-78 is a specific and effective direct AMPK activator (EC50: 25 μM). MT 63-78 blocks prostate cancer growth by inhibiting the lipogenesis and mTORC1 pathways. MT 63-78 has antitumor effects. MT 63–78 also causes cell mitotic arrest and apoptosis.
Host
Item no.
Amount 100 mg
Available
MT 63-­78 Login MT 63-78
Type Chemicals
Clone
Specific against Other
Appl. MT 63-78 is a specific and effective direct AMPK activator (EC50: 25 μM). MT 63-78 blocks prostate cancer growth by inhibiting the lipogenesis and mTORC1 pathways. MT 63-78 has antitumor effects. MT 63–78 also causes cell mitotic arrest and apoptosis.
Host
Item no.
Amount 250 mg
Available
MT 63-­78 Login MT 63-78
Type Chemicals
Clone
Specific against Other
Appl. MT 63-78 is a specific and effective direct AMPK activator (EC50: 25 μM). MT 63-78 blocks prostate cancer growth by inhibiting the lipogenesis and mTORC1 pathways. MT 63-78 has antitumor effects. MT 63–78 also causes cell mitotic arrest and apoptosis.
Host
Item no.
Amount 1 g
Available
Lu AF27139 Login Lu AF27139
Type Chemicals
Clone
Specific against Other
Appl. IV
Host
Item no.
Amount 100 mg
Available
Lu AF27139 Login Lu AF27139
Type Chemicals
Clone
Specific against Other
Appl. IV
Host
Item no.
Amount 250 mg
Available
Lu AF27139 Login Lu AF27139
Type Chemicals
Clone
Specific against Other
Appl. IV
Host
Item no.
Amount 1 g
Available
Rasarfin Login Rasarfin
Type Chemicals
Clone
Specific against Other
Appl. other
Host
Item no.
Amount 100 mg
Available
Rasarfin Login Rasarfin
Type Chemicals
Clone
Specific against Other
Appl. other
Host
Item no.
Amount 250 mg
Available
Rasarfin Login Rasarfin
Type Chemicals
Clone
Specific against Other
Appl. other
Host
Item no.
Amount 1 g
Available
K-­975 Login K-975
Type Chemicals
Clone
Specific against Other
Appl. K-975 is a first-in-class TEAD inhibitor, directly inhibiting YAP/TAZ-TEAD protein-protein interaction and showing a potent anti-tumor effect in malignant pleural mesothelioma. K-975 was covalently bound to an internal cysteine residue located in the palmitate-binding pocket of TEAD. K-975 had a
Host
Item no.
Amount 100 mg
Available
K-­975 Login K-975
Type Chemicals
Clone
Specific against Other
Appl. K-975 is a first-in-class TEAD inhibitor, directly inhibiting YAP/TAZ-TEAD protein-protein interaction and showing a potent anti-tumor effect in malignant pleural mesothelioma. K-975 was covalently bound to an internal cysteine residue located in the palmitate-binding pocket of TEAD. K-975 had a
Host
Item no.
Amount 250 mg
Available
K-­975 Login K-975
Type Chemicals
Clone
Specific against Other
Appl. K-975 is a first-in-class TEAD inhibitor, directly inhibiting YAP/TAZ-TEAD protein-protein interaction and showing a potent anti-tumor effect in malignant pleural mesothelioma. K-975 was covalently bound to an internal cysteine residue located in the palmitate-binding pocket of TEAD. K-975 had a
Host
Item no.
Amount 1 g
Available
GPR52-­IN-­43(CAY10786) Login GPR52-IN-43(CAY10786)
Type Chemicals
Clone
Specific against Other
Appl. GPR52-IN-43(CAY10786) is a novel GPR52 antagonist, reducing mHTT levels by targeting GPR52 and promoting survival of mouse primary striatal neurons, and also reducing HD-related phenotypes in HdhQ140.
Host
Item no.
Amount 100 mg
Available
GPR52-­IN-­43(CAY10786) Login GPR52-IN-43(CAY10786)
Type Chemicals
Clone
Specific against Other
Appl. GPR52-IN-43(CAY10786) is a novel GPR52 antagonist, reducing mHTT levels by targeting GPR52 and promoting survival of mouse primary striatal neurons, and also reducing HD-related phenotypes in HdhQ140.
Host
Item no.
Amount 250 mg
Available
GPR52-­IN-­43(CAY10786) Login GPR52-IN-43(CAY10786)
Type Chemicals
Clone
Specific against Other
Appl. GPR52-IN-43(CAY10786) is a novel GPR52 antagonist, reducing mHTT levels by targeting GPR52 and promoting survival of mouse primary striatal neurons, and also reducing HD-related phenotypes in HdhQ140.
Host
Item no.
Amount 1 g
Available

1437732 Item(s)

per page

Page:
  1. 38
  2. 39
  3. 40
  4. 41
  5. 42
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