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1437732 Item(s)

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  2. 28
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  4. 30
  5. 31
Name PDF Type Clone Specific against Appl. Host Item no. Amount ✓ Price
TDI-­011536 Chemicals Other TDI-011536 is a potent Lats kinase inhibitor, interrupts Hippo-Yap signaling and initiates the proliferation of lesioned heartmuscle cells. TDI-011536 can be used in studies of organ conservation and regeneration. DCC-DC72006-100mg

DCChemicals 		100 mg Login
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TDI-­011536 Chemicals Other TDI-011536 is a potent Lats kinase inhibitor, interrupts Hippo-Yap signaling and initiates the proliferation of lesioned heartmuscle cells. TDI-011536 can be used in studies of organ conservation and regeneration. DCC-DC72006-250mg

DCChemicals 		250 mg Login
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TDI-­011536 Chemicals Other TDI-011536 is a potent Lats kinase inhibitor, interrupts Hippo-Yap signaling and initiates the proliferation of lesioned heartmuscle cells. TDI-011536 can be used in studies of organ conservation and regeneration. DCC-DC72006-1g

DCChemicals 		1 g Login
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VK-­II-­86 Chemicals Other other DCC-DC70883-100mg

DCChemicals 		100 mg Login
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VK-­II-­86 Chemicals Other other DCC-DC70883-250mg

DCChemicals 		250 mg Login
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VK-­II-­86 Chemicals Other other DCC-DC70883-1g

DCChemicals 		1 g Login
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ML353 (VU0478006) Chemicals Other ML353 (VU0478006) is a ovel Silent Allosteric Modulator (SAM) of the Metabotropic Glutamate Receptor 5. DCC-DC60171-10mg

DCChemicals 		10 mg Login
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ML353 (VU0478006) Chemicals Other ML353 (VU0478006) is a ovel Silent Allosteric Modulator (SAM) of the Metabotropic Glutamate Receptor 5. DCC-DC60171-50mg

DCChemicals 		50 mg Login
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ML353 (VU0478006) Chemicals Other ML353 (VU0478006) is a ovel Silent Allosteric Modulator (SAM) of the Metabotropic Glutamate Receptor 5. DCC-DC60171-100mg

DCChemicals 		100 mg Login
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GR-­103545 fumarate Chemicals Other DCC-DC60183-100mg

DCChemicals 		100 mg Login
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Y 39983HCl Chemicals Other Y-39983, also known as Y-33075, is a potent and selective inhibitor of ROCK family with IC50 value of 3.6nM for ROCK. Y-39983 attenuates experimental autoimmune encephalomyelitis via inhibition of demyelination. Y-39983 downregulates RhoA/Rho-associated kinase expression during its prom, promotes regeneration of crushed axons of retinal ganglion cells into the optic nerve of adult cats. DCC-DC60182-100mg

DCChemicals 		100 mg Login
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Y 39983HCl Chemicals Other Y-39983, also known as Y-33075, promotes regeneration of crushed axons of retinal ganglion cells into the optic nerve of adult cats., is a potent and selective inhibitor of ROCK family with IC50 value of 3.6nM for ROCK. Y-39983 attenuates experimental autoimmune encephalomyelitis via inhibition of demyelination. Y-39983 downregulates RhoA/Rho-associated kinase expression during its prom DCC-DC60182-250mg

DCChemicals 		250 mg Login
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Y 39983HCl Chemicals Other Y-39983, also known as Y-33075, promotes regeneration of crushed axons of retinal ganglion cells into the optic nerve of adult cats., is a potent and selective inhibitor of ROCK family with IC50 value of 3.6nM for ROCK. Y-39983 attenuates experimental autoimmune encephalomyelitis via inhibition of demyelination. Y-39983 downregulates RhoA/Rho-associated kinase expression during its prom DCC-DC60182-1g

DCChemicals 		1 g Login
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dCBP-­1 Chemicals Other dCBP-1 is a potent and selective heterobifunctional degrader of p300/CBP based on Cereblon ligand. dCBP-1 is exceptionally potent at killing multiple myeloma cells and can abolish the enhancer that drives MYC oncogene expression. As an efficient degrader , dCBP-1 is a useful tool alongside domain inhibitors for dissecting the mechanism by which these factors coordinate enhancer activity in normal and diseased cells. DCC-DC60181-100mg

DCChemicals 		100 mg Login
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Tuspetinib(HM43239) Chemicals Other HM43239 is an orally active small molecule inhibitor of FLT3 that selectively inhibits not only FLT3 wild type, ITD mutants or TKD mutations, but also FLT3 ITD/TKD double mutations. HM43239 directly inhibits the kinase activity of FLT3 as a reversible Type I inhibitor and effectively modulates downstream p-STAT5 and p-ERK. HM43239 also demonstrated inhibition of SYK, JAK1/2 and TAK1, known to be involved in tumor cell proliferation and/or differentiation HM43239 monotherapy induced dose-dependent regression of tumor growth in FLT3 wild-type and FLT3 mutated leukemia cancer cell line. DCC-DC60179-100mg

DCChemicals 		100 mg Login
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Tuspetinib(HM43239) Chemicals Other HM43239 is an orally active small molecule inhibitor of FLT3 that selectively inhibits not only FLT3 wild type, ITD mutants or TKD mutations, but also FLT3 ITD/TKD double mutations. HM43239 directly inhibits the kinase activity of FLT3 as a reversible Type I inhibitor and effectively modulates downstream p-STAT5 and p-ERK. HM43239 also demonstrated inhibition of SYK, JAK1/2 and TAK1, known to be involved in tumor cell proliferation and/or differentiation HM43239 monotherapy induced dose-dependent regression of tumor growth in FLT3 wild-type and FLT3 mutated leukemia cancer cell line. DCC-DC60179-250mg

DCChemicals 		250 mg Login
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Tuspetinib(HM43239) Chemicals Other HM43239 is an orally active small molecule inhibitor of FLT3 that selectively inhibits not only FLT3 wild type, ITD mutants or TKD mutations, but also FLT3 ITD/TKD double mutations. HM43239 directly inhibits the kinase activity of FLT3 as a reversible Type I inhibitor and effectively modulates downstream p-STAT5 and p-ERK. HM43239 also demonstrated inhibition of SYK, JAK1/2 and TAK1, known to be involved in tumor cell proliferation and/or differentiation HM43239 monotherapy induced dose-dependent regression of tumor growth in FLT3 wild-type and FLT3 mutated leukemia cancer cell line. DCC-DC60179-1g

DCChemicals 		1 g Login
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MCULE-­3408819416 Chemicals Other MCULE-3408819416|DC Chemicals DCC-DC60144-100mg

DCChemicals 		100 mg Login
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GW805758X Chemicals Other GW805758|DC Chemicals DCC-DC60145-100mg

DCChemicals 		100 mg Login
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VK-­28 Chemicals Other DCC-DC60175-100mg

DCChemicals 		100 mg Login
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Propanoic acid, 3-­[[[(phenylmethyl)thio]thioxomethyl]thio]-­ Chemicals Other DCC-DC60170-100mg

DCChemicals 		100 mg Login
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ethyl 2-­ethoxycarbothioylsulfanylpropanoate Chemicals Other DCC-DC60168-100mg

DCChemicals 		100 mg Login
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Benzene, 1-­[(1R)-­1-­(bromomethoxy)ethyl]-­3,5-­bis(trifluoromethyl)-­ Chemicals Other DCC-DC60167-100mg

DCChemicals 		100 mg Login
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Benzenecarbodithioicacid, phenylmethyl ester Chemicals Other DCC-DC60166-100mg

DCChemicals 		100 mg Login
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FPPS-­IN-­11 Chemicals Other DCC-DC60163-100mg

DCChemicals 		100 mg Login
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Name Price
TDI-­011536 Login TDI-011536
Type Chemicals
Clone
Specific against Other
Appl. TDI-011536 is a potent Lats kinase inhibitor, interrupts Hippo-Yap signaling and initiates the proliferation of lesioned heartmuscle cells. TDI-011536 can be used in studies of organ conservation and regeneration.
Host
Item no.
Amount 100 mg
Available
TDI-­011536 Login TDI-011536
Type Chemicals
Clone
Specific against Other
Appl. TDI-011536 is a potent Lats kinase inhibitor, interrupts Hippo-Yap signaling and initiates the proliferation of lesioned heartmuscle cells. TDI-011536 can be used in studies of organ conservation and regeneration.
Host
Item no.
Amount 250 mg
Available
TDI-­011536 Login TDI-011536
Type Chemicals
Clone
Specific against Other
Appl. TDI-011536 is a potent Lats kinase inhibitor, interrupts Hippo-Yap signaling and initiates the proliferation of lesioned heartmuscle cells. TDI-011536 can be used in studies of organ conservation and regeneration.
Host
Item no.
Amount 1 g
Available
VK-­II-­86 Login VK-II-86
Type Chemicals
Clone
Specific against Other
Appl. other
Host
Item no.
Amount 100 mg
Available
VK-­II-­86 Login VK-II-86
Type Chemicals
Clone
Specific against Other
Appl. other
Host
Item no.
Amount 250 mg
Available
VK-­II-­86 Login VK-II-86
Type Chemicals
Clone
Specific against Other
Appl. other
Host
Item no.
Amount 1 g
Available
ML353 (VU0478006) Login ML353 (VU0478006)
Type Chemicals
Clone
Specific against Other
Appl. ML353 (VU0478006) is a ovel Silent Allosteric Modulator (SAM) of the Metabotropic Glutamate Receptor 5.
Host
Item no.
Amount 10 mg
Available
ML353 (VU0478006) Login ML353 (VU0478006)
Type Chemicals
Clone
Specific against Other
Appl. ML353 (VU0478006) is a ovel Silent Allosteric Modulator (SAM) of the Metabotropic Glutamate Receptor 5.
Host
Item no.
Amount 50 mg
Available
ML353 (VU0478006) Login ML353 (VU0478006)
Type Chemicals
Clone
Specific against Other
Appl. ML353 (VU0478006) is a ovel Silent Allosteric Modulator (SAM) of the Metabotropic Glutamate Receptor 5.
Host
Item no.
Amount 100 mg
Available
GR-­103545 fumarate Login GR-103545 fumarate
Type Chemicals
Clone
Specific against Other
Appl.
Host
Item no.
Amount 100 mg
Available
Y 39983HCl Login Y 39983HCl
Type Chemicals
Clone
Specific against Other
Appl. Y-39983, also known as Y-33075, is a potent and selective inhibitor of ROCK family with IC50 value of 3.6nM for ROCK. Y-39983 attenuates experimental autoimmune encephalomyelitis via inhibition of demyelination. Y-39983 downregulates RhoA/Rho-associated kinase expression during its prom, promotes regeneration of crushed axons of retinal ganglion cells into the optic nerve of adult cats.
Host
Item no.
Amount 100 mg
Available
Y 39983HCl Login Y 39983HCl
Type Chemicals
Clone
Specific against Other
Appl. Y-39983, also known as Y-33075, promotes regeneration of crushed axons of retinal ganglion cells into the optic nerve of adult cats., is a potent and selective inhibitor of ROCK family with IC50 value of 3.6nM for ROCK. Y-39983 attenuates experimental autoimmune encephalomyelitis via inhibition of demyelination. Y-39983 downregulates RhoA/Rho-associated kinase expression during its prom
Host
Item no.
Amount 250 mg
Available
Y 39983HCl Login Y 39983HCl
Type Chemicals
Clone
Specific against Other
Appl. Y-39983, also known as Y-33075, promotes regeneration of crushed axons of retinal ganglion cells into the optic nerve of adult cats., is a potent and selective inhibitor of ROCK family with IC50 value of 3.6nM for ROCK. Y-39983 attenuates experimental autoimmune encephalomyelitis via inhibition of demyelination. Y-39983 downregulates RhoA/Rho-associated kinase expression during its prom
Host
Item no.
Amount 1 g
Available
dCBP-­1 Login dCBP-1
Type Chemicals
Clone
Specific against Other
Appl. dCBP-1 is a potent and selective heterobifunctional degrader of p300/CBP based on Cereblon ligand. dCBP-1 is exceptionally potent at killing multiple myeloma cells and can abolish the enhancer that drives MYC oncogene expression. As an efficient degrader , dCBP-1 is a useful tool alongside domain inhibitors for dissecting the mechanism by which these factors coordinate enhancer activity in normal and diseased cells.
Host
Item no.
Amount 100 mg
Available
Tuspetinib(HM43239) Login Tuspetinib(HM43239)
Type Chemicals
Clone
Specific against Other
Appl. HM43239 is an orally active small molecule inhibitor of FLT3 that selectively inhibits not only FLT3 wild type, ITD mutants or TKD mutations, but also FLT3 ITD/TKD double mutations. HM43239 directly inhibits the kinase activity of FLT3 as a reversible Type I inhibitor and effectively modulates downstream p-STAT5 and p-ERK. HM43239 also demonstrated inhibition of SYK, JAK1/2 and TAK1, known to be involved in tumor cell proliferation and/or differentiation HM43239 monotherapy induced dose-dependent regression of tumor growth in FLT3 wild-type and FLT3 mutated leukemia cancer cell line.
Host
Item no.
Amount 100 mg
Available
Tuspetinib(HM43239) Login Tuspetinib(HM43239)
Type Chemicals
Clone
Specific against Other
Appl. HM43239 is an orally active small molecule inhibitor of FLT3 that selectively inhibits not only FLT3 wild type, ITD mutants or TKD mutations, but also FLT3 ITD/TKD double mutations. HM43239 directly inhibits the kinase activity of FLT3 as a reversible Type I inhibitor and effectively modulates downstream p-STAT5 and p-ERK. HM43239 also demonstrated inhibition of SYK, JAK1/2 and TAK1, known to be involved in tumor cell proliferation and/or differentiation HM43239 monotherapy induced dose-dependent regression of tumor growth in FLT3 wild-type and FLT3 mutated leukemia cancer cell line.
Host
Item no.
Amount 250 mg
Available
Tuspetinib(HM43239) Login Tuspetinib(HM43239)
Type Chemicals
Clone
Specific against Other
Appl. HM43239 is an orally active small molecule inhibitor of FLT3 that selectively inhibits not only FLT3 wild type, ITD mutants or TKD mutations, but also FLT3 ITD/TKD double mutations. HM43239 directly inhibits the kinase activity of FLT3 as a reversible Type I inhibitor and effectively modulates downstream p-STAT5 and p-ERK. HM43239 also demonstrated inhibition of SYK, JAK1/2 and TAK1, known to be involved in tumor cell proliferation and/or differentiation HM43239 monotherapy induced dose-dependent regression of tumor growth in FLT3 wild-type and FLT3 mutated leukemia cancer cell line.
Host
Item no.
Amount 1 g
Available
MCULE-­3408819416 Login MCULE-3408819416
Type Chemicals
Clone
Specific against Other
Appl. MCULE-3408819416|DC Chemicals
Host
Item no.
Amount 100 mg
Available
GW805758X Login GW805758X
Type Chemicals
Clone
Specific against Other
Appl. GW805758|DC Chemicals
Host
Item no.
Amount 100 mg
Available
VK-­28 Login VK-28
Type Chemicals
Clone
Specific against Other
Appl.
Host
Item no.
Amount 100 mg
Available
Propanoic acid, 3-­[[[(phenylmethyl)thio]thioxomethyl]thio]-­ Login Propanoic acid, 3-[[[(phenylmethyl)thio]thioxomethyl]thio]-
Type Chemicals
Clone
Specific against Other
Appl.
Host
Item no.
Amount 100 mg
Available
ethyl 2-­ethoxycarbothioylsulfanylpropanoate Login ethyl 2-ethoxycarbothioylsulfanylpropanoate
Type Chemicals
Clone
Specific against Other
Appl.
Host
Item no.
Amount 100 mg
Available
Benzene, 1-­[(1R)-­1-­(bromomethoxy)ethyl]-­3,5-­bis(trifluoromethyl)-­ Login Benzene, 1-[(1R)-1-(bromomethoxy)ethyl]-3,5-bis(trifluoromethyl)-
Type Chemicals
Clone
Specific against Other
Appl.
Host
Item no.
Amount 100 mg
Available
Benzenecarbodithioicacid, phenylmethyl ester Login Benzenecarbodithioicacid, phenylmethyl ester
Type Chemicals
Clone
Specific against Other
Appl.
Host
Item no.
Amount 100 mg
Available
FPPS-­IN-­11 Login FPPS-IN-11
Type Chemicals
Clone
Specific against Other
Appl.
Host
Item no.
Amount 100 mg
Available

1437732 Item(s)

per page

Page:
  1. 27
  2. 28
  3. 29
  4. 30
  5. 31
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