Reagents (3)

(±)-Nutlin-3

Reference: 10004372-50

€0.00 (tax incl.)

An inhibitor of p53-Mdm2 interaction (IC50 = 0.09 µM); induces the expression of p53-regulated genes and exhibits potent antiproliferative activity in cells with functional p53

Sulindac

Reference: 10004386-1

€0.00 (tax incl.)

A non-selective inhibitor of both COX-1 and COX-2 with extensive epidemiology documenting its effective reduction of human colorectal cancer

Sulindac

Reference: 10004386-10

€0.00 (tax incl.)

A non-selective inhibitor of both COX-1 and COX-2 with extensive epidemiology documenting its effective reduction of human colorectal cancer

Sulindac

Reference: 10004386-5

€0.00 (tax incl.)

A non-selective inhibitor of both COX-1 and COX-2 with extensive epidemiology documenting its effective reduction of human colorectal cancer

Sulindac

Reference: 10004386-50

€0.00 (tax incl.)

A non-selective inhibitor of both COX-1 and COX-2 with extensive epidemiology documenting its effective reduction of human colorectal cancer

A metabolite of sulindac that inhibits both COX-1 and COX-2 (IC50s = 1.9 and 1.21 µM, respectively); also inhibits aldose reductase (IC50 = 279 nM), blocking NADPH-dependent reduction of glucose to sorbitol, and...

Sulindac sulfide

Reference: 10004387-10

€0.00 (tax incl.)

A metabolite of sulindac that inhibits both COX-1 and COX-2 (IC50s = 1.9 and 1.21 µM, respectively); also inhibits aldose reductase (IC50 = 279 nM), blocking NADPH-dependent reduction of glucose to sorbitol, and...

Sulindac sulfide

Reference: 10004387-25

€0.00 (tax incl.)

A metabolite of sulindac that inhibits both COX-1 and COX-2 (IC50s = 1.9 and 1.21 µM, respectively); also inhibits aldose reductase (IC50 = 279 nM), blocking NADPH-dependent reduction of glucose to sorbitol, and...

Sulindac sulfide

Reference: 10004387-5

€0.00 (tax incl.)

A metabolite of sulindac that inhibits both COX-1 and COX-2 (IC50s = 1.9 and 1.21 µM, respectively); also inhibits aldose reductase (IC50 = 279 nM), blocking NADPH-dependent reduction of glucose to sorbitol, and...

Reversine

Reference: 10004412-1

€0.00 (tax incl.)

A purine derivative; induces differentiation or dedifferentiation, depending on cell type; inhibits the Aurora A, B, and C kinases with IC50 values of 98-876 nM; A3 receptor antagonist (Ki = 0.66 µM); inhibits MPS1...

Reversine

Reference: 10004412-10

€0.00 (tax incl.)

A purine derivative; induces differentiation or dedifferentiation, depending on cell type; inhibits the Aurora A, B, and C kinases with IC50 values of 98-876 nM; A3 receptor antagonist (Ki = 0.66 µM); inhibits MPS1...

Reversine

Reference: 10004412-25

€0.00 (tax incl.)

A purine derivative; induces differentiation or dedifferentiation, depending on cell type; inhibits the Aurora A, B, and C kinases with IC50 values of 98-876 nM; A3 receptor antagonist (Ki = 0.66 µM); inhibits MPS1...

Reversine

Reference: 10004412-5

€0.00 (tax incl.)

A purine derivative; induces differentiation or dedifferentiation, depending on cell type; inhibits the Aurora A, B, and C kinases with IC50 values of 98-876 nM; A3 receptor antagonist (Ki = 0.66 µM); inhibits MPS1...

NADP+ (sodium salt hydrate)

Reference: 10004675-1

€0.00 (tax incl.)

The oxidized form of NADPH; serves as a cofactor in various biological reactions

NADP+ (sodium salt hydrate)

Reference: 10004675-100

€0.00 (tax incl.)

The oxidized form of NADPH; serves as a cofactor in various biological reactions

NADP+ (sodium salt hydrate)

Reference: 10004675-250

€0.00 (tax incl.)

The oxidized form of NADPH; serves as a cofactor in various biological reactions

NADP+ (sodium salt hydrate)

Reference: 10004675-50

€0.00 (tax incl.)

The oxidized form of NADPH; serves as a cofactor in various biological reactions

FMOC-L-Leucine

Reference: 10004888-100

€0.00 (tax incl.)

A partial agonist of PPARγ; activates PPARγ with a lower potency (Ki = 15 versus 0.035 µM) but a similar maximal efficacy compared to rosiglitazone; improves insulin resistance in normal, diet-induced...

FMOC-L-Leucine

Reference: 10004888-25

€0.00 (tax incl.)

A partial agonist of PPARγ; activates PPARγ with a lower potency (Ki = 15 versus 0.035 µM) but a similar maximal efficacy compared to rosiglitazone; improves insulin resistance in normal, diet-induced...

FMOC-L-Leucine

Reference: 10004888-50

€0.00 (tax incl.)

A partial agonist of PPARγ; activates PPARγ with a lower potency (Ki = 15 versus 0.035 µM) but a similar maximal efficacy compared to rosiglitazone; improves insulin resistance in normal, diet-induced...

O-1918

Reference: 10004914-1

€0.00 (tax incl.)

A cannabidiol (CBD) analog that acts as a selective antagonist of abnormal CBD (Abn-CBD) at the non-CB1/CB2 endothelial receptor; does not bind to CB1 or CB2 receptors at concentrations up to 30 µM and inhibits the...

O-1918

Reference: 10004914-10

€0.00 (tax incl.)

A cannabidiol (CBD) analog that acts as a selective antagonist of abnormal CBD (Abn-CBD) at the non-CB1/CB2 endothelial receptor; does not bind to CB1 or CB2 receptors at concentrations up to 30 µM and inhibits the...

O-1918

Reference: 10004914-25

€0.00 (tax incl.)

A cannabidiol (CBD) analog that acts as a selective antagonist of abnormal CBD (Abn-CBD) at the non-CB1/CB2 endothelial receptor; does not bind to CB1 or CB2 receptors at concentrations up to 30 µM and inhibits the...

O-1918

Reference: 10004914-5

€0.00 (tax incl.)

A cannabidiol (CBD) analog that acts as a selective antagonist of abnormal CBD (Abn-CBD) at the non-CB1/CB2 endothelial receptor; does not bind to CB1 or CB2 receptors at concentrations up to 30 µM and inhibits the...

N,N'-Dicyclohexylurea

Reference: 10004971-10

€0.00 (tax incl.)

A selective sEH inhibitor with IC50 values of 160 and 90 nM for recombinant human and mouse sEH, respectively; at 10 µM, blocks the hydrolysis of cis- and trans-EETs and completely inhibits 14,(15)-EET-induced PPAR...

N,N'-Dicyclohexylurea

Reference: 10004971-25

€0.00 (tax incl.)

A selective sEH inhibitor with IC50 values of 160 and 90 nM for recombinant human and mouse sEH, respectively; at 10 µM, blocks the hydrolysis of cis- and trans-EETs and completely inhibits 14,(15)-EET-induced PPAR...

Ionomycin

Reference: 10004974-1

€0.00 (tax incl.)

A selective calcium ionophore that mobilizes intracellular calcium stores. It is used as a research tool to raise the intracellular level of calcium, to study calcium transport across biological membranes, and to...

Ionomycin

Reference: 10004974-10

€0.00 (tax incl.)

A selective calcium ionophore that mobilizes intracellular calcium stores. It is used as a research tool to raise the intracellular level of calcium, to study calcium transport across biological membranes, and to...

Ionomycin

Reference: 10004974-25

€0.00 (tax incl.)

A selective calcium ionophore that mobilizes intracellular calcium stores. It is used as a research tool to raise the intracellular level of calcium, to study calcium transport across biological membranes, and to...

Ionomycin

Reference: 10004974-5

€0.00 (tax incl.)

A selective calcium ionophore that mobilizes intracellular calcium stores. It is used as a research tool to raise the intracellular level of calcium, to study calcium transport across biological membranes, and to...

Leptomycin B

Reference: 10004976-10

€0.00 (tax incl.)

A potent anti-fungal antibiotic that can directly block nuclear transport by inhibiting the action of CRM1

Leptomycin B

Reference: 10004976-25

€0.00 (tax incl.)

A potent anti-fungal antibiotic that can directly block nuclear transport by inhibiting the action of CRM1

Leptomycin B

Reference: 10004976-5

€0.00 (tax incl.)

A potent anti-fungal antibiotic that can directly block nuclear transport by inhibiting the action of CRM1

Caylin-1

Reference: 10004985-1

€0.00 (tax incl.)

A nutlin-3 analog; inhibits the growth of HCT116 cells at high concentrations (IC50 = ~7 µM); promotes the growth of HCT-116 cells ~20% at concentrations at or below 1 µM

Caylin-1

Reference: 10004985-10

€0.00 (tax incl.)

A nutlin-3 analog; inhibits the growth of HCT116 cells at high concentrations (IC50 = ~7 µM); promotes the growth of HCT-116 cells ~20% at concentrations at or below 1 µM

Caylin-1

Reference: 10004985-5

€0.00 (tax incl.)

A nutlin-3 analog; inhibits the growth of HCT116 cells at high concentrations (IC50 = ~7 µM); promotes the growth of HCT-116 cells ~20% at concentrations at or below 1 µM

Caylin-2

Reference: 10005002-1

€0.00 (tax incl.)

A nutlin-3 analog; inhibits the growth of HCT116 cells at high concentrations (IC50 = ~8 µM); promotes the growth of HCT116 cells ~40% at concentrations between 5-100 nM

Caylin-2

Reference: 10005002-10

€0.00 (tax incl.)

A nutlin-3 analog; inhibits the growth of HCT116 cells at high concentrations (IC50 = ~8 µM); promotes the growth of HCT116 cells ~40% at concentrations between 5-100 nM

Caylin-2

Reference: 10005002-5

€0.00 (tax incl.)

A nutlin-3 analog; inhibits the growth of HCT116 cells at high concentrations (IC50 = ~8 µM); promotes the growth of HCT116 cells ~40% at concentrations between 5-100 nM

BML-210

Reference: 10005019-1

€0.00 (tax incl.)

An HDAC inhibitor with an IC50 value of 30 µM when tested in HeLa cell nuclear extracts using 200 µM acetylated fluorometric substrate

BML-210

Reference: 10005019-10

€0.00 (tax incl.)

An HDAC inhibitor with an IC50 value of 30 µM when tested in HeLa cell nuclear extracts using 200 µM acetylated fluorometric substrate

BML-210

Reference: 10005019-25

€0.00 (tax incl.)

An HDAC inhibitor with an IC50 value of 30 µM when tested in HeLa cell nuclear extracts using 200 µM acetylated fluorometric substrate

BML-210

Reference: 10005019-5

€0.00 (tax incl.)

An HDAC inhibitor with an IC50 value of 30 µM when tested in HeLa cell nuclear extracts using 200 µM acetylated fluorometric substrate

L-NMMA (acetate)

Reference: 10005031-100

€0.00 (tax incl.)

A relatively non-selective inhibitor of all NOS isoforms with Ki values 0.18, 0.4, and 6 µM for nNOs (rat), eNOS (human), and iNOS (mouse), respectively

L-NMMA (acetate)

Reference: 10005031-25

€0.00 (tax incl.)

A relatively non-selective inhibitor of all NOS isoforms with Ki values 0.18, 0.4, and 6 µM for nNOs (rat), eNOS (human), and iNOS (mouse), respectively

L-NMMA (acetate)

Reference: 10005031-5

€0.00 (tax incl.)

A relatively non-selective inhibitor of all NOS isoforms with Ki values 0.18, 0.4, and 6 µM for nNOs (rat), eNOS (human), and iNOS (mouse), respectively

L-NMMA (acetate)

Reference: 10005031-50

€0.00 (tax incl.)

A relatively non-selective inhibitor of all NOS isoforms with Ki values 0.18, 0.4, and 6 µM for nNOs (rat), eNOS (human), and iNOS (mouse), respectively

CAY10444

Reference: 10005033-10

€0.00 (tax incl.)

A selective antagonist of S1P binding to the S1P3 receptor; blocks calcium increase in HeLa cells by about 40% at 10 µM

CAY10444

Reference: 10005033-25

€0.00 (tax incl.)

A selective antagonist of S1P binding to the S1P3 receptor; blocks calcium increase in HeLa cells by about 40% at 10 µM

CAY10444

Reference: 10005033-5

€0.00 (tax incl.)

A selective antagonist of S1P binding to the S1P3 receptor; blocks calcium increase in HeLa cells by about 40% at 10 µM

CAY10444

Reference: 10005033-50

€0.00 (tax incl.)

A selective antagonist of S1P binding to the S1P3 receptor; blocks calcium increase in HeLa cells by about 40% at 10 µM

CAY10434

Reference: 10005067-1

€0.00 (tax incl.)

A selective inhibitor of the 20-HETE synthase, CYP4A11, exhibiting an IC50 values of 8.8 nM when tested in human renal microsomes

CAY10434

Reference: 10005067-10

€0.00 (tax incl.)

A selective inhibitor of the 20-HETE synthase, CYP4A11, exhibiting an IC50 values of 8.8 nM when tested in human renal microsomes

CAY10434

Reference: 10005067-5

€0.00 (tax incl.)

A selective inhibitor of the 20-HETE synthase, CYP4A11, exhibiting an IC50 values of 8.8 nM when tested in human renal microsomes

CAY10434

Reference: 10005067-50

€0.00 (tax incl.)

A selective inhibitor of the 20-HETE synthase, CYP4A11, exhibiting an IC50 values of 8.8 nM when tested in human renal microsomes

CAY10455

Reference: 10005072-1

€0.00 (tax incl.)

A labeled analog of AEA that is non-fluorescent when outside the cell but upon transport into the cell, is cleaved by esterases to give a bright fluorescence at 530 nm; used as an alternative substrate to study AEA...

CAY10455

Reference: 10005072-100

€0.00 (tax incl.)

A labeled analog of AEA that is non-fluorescent when outside the cell but upon transport into the cell, is cleaved by esterases to give a bright fluorescence at 530 nm; used as an alternative substrate to study AEA...

CAY10455

Reference: 10005072-500

€0.00 (tax incl.)

A labeled analog of AEA that is non-fluorescent when outside the cell but upon transport into the cell, is cleaved by esterases to give a bright fluorescence at 530 nm; used as an alternative substrate to study AEA...

CAY10435

Reference: 10005102-1

€0.00 (tax incl.)

A selective, potent inhibitor of rat FAAH (Ki = 0.57 nM); exhibited IC50 values of 0.81, 83 nM, and 50 µM for FAAH, TGH, and an uncharacterized hydrolase (KIAA1363), respectively, when screened against the serine...

CAY10435

Reference: 10005102-10

€0.00 (tax incl.)

A selective, potent inhibitor of rat FAAH (Ki = 0.57 nM); exhibited IC50 values of 0.81, 83 nM, and 50 µM for FAAH, TGH, and an uncharacterized hydrolase (KIAA1363), respectively, when screened against the serine...

CAY10435

Reference: 10005102-5

€0.00 (tax incl.)

A selective, potent inhibitor of rat FAAH (Ki = 0.57 nM); exhibited IC50 values of 0.81, 83 nM, and 50 µM for FAAH, TGH, and an uncharacterized hydrolase (KIAA1363), respectively, when screened against the serine...

CAY10435

Reference: 10005102-500

€0.00 (tax incl.)

A selective, potent inhibitor of rat FAAH (Ki = 0.57 nM); exhibited IC50 values of 0.81, 83 nM, and 50 µM for FAAH, TGH, and an uncharacterized hydrolase (KIAA1363), respectively, when screened against the serine...

Daidzein

Reference: 10005166-100

€0.00 (tax incl.)

An isoflavone; binds to ERβ (Ki = 2.8 µM) but not ERα up to 1 mM; estrogenic in vitro, increasing ERE-mediated gene transcription via ERβ (EC50 = 2.8 µM); an inhibitor of CAVII and CAXII (Kis = 4.2 and 56 nM,...

Daidzein

Reference: 10005166-1

€0.00 (tax incl.)

An isoflavone; binds to ERβ (Ki = 2.8 µM) but not ERα up to 1 mM; estrogenic in vitro, increasing ERE-mediated gene transcription via ERβ (EC50 = 2.8 µM); an inhibitor of CAVII and CAXII (Kis = 4.2 and 56 nM,...

Daidzein

Reference: 10005166-500

€0.00 (tax incl.)

An isoflavone; binds to ERβ (Ki = 2.8 µM) but not ERα up to 1 mM; estrogenic in vitro, increasing ERE-mediated gene transcription via ERβ (EC50 = 2.8 µM); an inhibitor of CAVII and CAXII (Kis = 4.2 and 56 nM,...

Daidzein

Reference: 10005166-5

€0.00 (tax incl.)

An isoflavone; binds to ERβ (Ki = 2.8 µM) but not ERα up to 1 mM; estrogenic in vitro, increasing ERE-mediated gene transcription via ERβ (EC50 = 2.8 µM); an inhibitor of CAVII and CAXII (Kis = 4.2 and 56 nM,...

Genistein

Reference: 10005167-100

€0.00 (tax incl.)

An isoflavonoid phytoestrogen with kinase inhibitory, anticancer, pro-cancer, hepatoprotective, and antiviral properties; inhibits EGFR, pp50v-Src, and pp110gag-fes (IC50s = 6, 7-8, and 6.5 µg/ml, respectively);...

Genistein

Reference: 10005167-1

€0.00 (tax incl.)

An isoflavonoid phytoestrogen with kinase inhibitory, anticancer, pro-cancer, hepatoprotective, and antiviral properties; inhibits EGFR, pp50v-Src, and pp110gag-fes (IC50s = 6, 7-8, and 6.5 µg/ml, respectively);...

Genistein

Reference: 10005167-250

€0.00 (tax incl.)

An isoflavonoid phytoestrogen with kinase inhibitory, anticancer, pro-cancer, hepatoprotective, and antiviral properties; inhibits EGFR, pp50v-Src, and pp110gag-fes (IC50s = 6, 7-8, and 6.5 µg/ml, respectively);...

Genistein

Reference: 10005167-500

€0.00 (tax incl.)

An isoflavonoid phytoestrogen with kinase inhibitory, anticancer, pro-cancer, hepatoprotective, and antiviral properties; inhibits EGFR, pp50v-Src, and pp110gag-fes (IC50s = 6, 7-8, and 6.5 µg/ml, respectively);...

Quercetin (hydrate)

Reference: 10005169-10

€0.00 (tax incl.)

A flavonoid; reduces autophagy, decreases the levels of ROS and MDA content, and increases total antioxidant capacity in the kidney in a mouse model of cadmium-induced autophagy at 5-100 mg/kg; reduces tumor growth in...

Quercetin (hydrate)

Reference: 10005169-100

€0.00 (tax incl.)

A flavonoid; reduces autophagy, decreases the levels of ROS and MDA content, and increases total antioxidant capacity in the kidney in a mouse model of cadmium-induced autophagy at 5-100 mg/kg; reduces tumor growth in...

Quercetin (hydrate)

Reference: 10005169-5

€0.00 (tax incl.)

A flavonoid; reduces autophagy, decreases the levels of ROS and MDA content, and increases total antioxidant capacity in the kidney in a mouse model of cadmium-induced autophagy at 5-100 mg/kg; reduces tumor growth in...

Quercetin (hydrate)

Reference: 10005169-50

€0.00 (tax incl.)

A flavonoid; reduces autophagy, decreases the levels of ROS and MDA content, and increases total antioxidant capacity in the kidney in a mouse model of cadmium-induced autophagy at 5-100 mg/kg; reduces tumor growth in...

Matairesinol

Reference: 10005174-1

€0.00 (tax incl.)

A lignan with diverse biological activities; reduces LPS-induced production of NO and PGE2 in RAW 264.7 cells; cytotoxic to colon 26 cancer cells (LC50 = 9 µg/ml); increases the lifespan of C. elegans at 100 µM;...

Matairesinol

Reference: 10005174-10

€0.00 (tax incl.)

A lignan with diverse biological activities; reduces LPS-induced production of NO and PGE2 in RAW 264.7 cells; cytotoxic to colon 26 cancer cells (LC50 = 9 µg/ml); increases the lifespan of C. elegans at 100 µM;...

Matairesinol

Reference: 10005174-25

€0.00 (tax incl.)

A lignan with diverse biological activities; reduces LPS-induced production of NO and PGE2 in RAW 264.7 cells; cytotoxic to colon 26 cancer cells (LC50 = 9 µg/ml); increases the lifespan of C. elegans at 100 µM;...

Matairesinol

Reference: 10005174-5

€0.00 (tax incl.)

A lignan with diverse biological activities; reduces LPS-induced production of NO and PGE2 in RAW 264.7 cells; cytotoxic to colon 26 cancer cells (LC50 = 9 µg/ml); increases the lifespan of C. elegans at 100 µM;...

CAY10441

Reference: 10005186-10

€0.00 (tax incl.)

A potent antagonist for the human IP (prostacyclin) receptor that antagonizes the carbaprostacyclin-induced activation of human neuroblastoma adenylate cyclase, blocking cAMP accumulation in a dose-dependent manner;...

CAY10441

Reference: 10005186-25

€0.00 (tax incl.)

A potent antagonist for the human IP (prostacyclin) receptor that antagonizes the carbaprostacyclin-induced activation of human neuroblastoma adenylate cyclase, blocking cAMP accumulation in a dose-dependent manner;...

CAY10441

Reference: 10005186-5

€0.00 (tax incl.)

A potent antagonist for the human IP (prostacyclin) receptor that antagonizes the carbaprostacyclin-induced activation of human neuroblastoma adenylate cyclase, blocking cAMP accumulation in a dose-dependent manner;...

CAY10441

Reference: 10005186-50

€0.00 (tax incl.)

A potent antagonist for the human IP (prostacyclin) receptor that antagonizes the carbaprostacyclin-induced activation of human neuroblastoma adenylate cyclase, blocking cAMP accumulation in a dose-dependent manner;...

PX-478

Reference: 10005189-1

€0.00 (tax incl.)

Suppresses both constitutive and hypoxia-induced levels of HIF-1α in cancer cells, resulting in reduced expression of HIF-1α target genes; increases chemo- or radiosensitivity of tumors

PX-478

Reference: 10005189-10

€0.00 (tax incl.)

Suppresses both constitutive and hypoxia-induced levels of HIF-1α in cancer cells, resulting in reduced expression of HIF-1α target genes; increases chemo- or radiosensitivity of tumors

PX-478

Reference: 10005189-25

€0.00 (tax incl.)

Suppresses both constitutive and hypoxia-induced levels of HIF-1α in cancer cells, resulting in reduced expression of HIF-1α target genes; increases chemo- or radiosensitivity of tumors

PX-478

Reference: 10005189-5

€0.00 (tax incl.)

Suppresses both constitutive and hypoxia-induced levels of HIF-1α in cancer cells, resulting in reduced expression of HIF-1α target genes; increases chemo- or radiosensitivity of tumors

2,3-DCPE (hydrochloride)

Reference: 10005229-10

€0.00 (tax incl.)

A proapoptoic compound with selectivity for cancer cells; induces apoptosis in vitro in various cancer cell lines (IC50 = 0.89-2.69 µM)

2,3-DCPE (hydrochloride)

Reference: 10005229-5

€0.00 (tax incl.)

A proapoptoic compound with selectivity for cancer cells; induces apoptosis in vitro in various cancer cell lines (IC50 = 0.89-2.69 µM)

2,3-DCPE (hydrochloride)

Reference: 10005229-50

€0.00 (tax incl.)

A proapoptoic compound with selectivity for cancer cells; induces apoptosis in vitro in various cancer cell lines (IC50 = 0.89-2.69 µM)

AFMK

Reference: 10005254-1

€0.00 (tax incl.)

A melatonin metabolite first identified in rat brain that has antioxidant and free radical scavenging activities in several experimental models; may be measured in plasma as an index of melatonin synthesis and...

AFMK

Reference: 10005254-10

€0.00 (tax incl.)

A melatonin metabolite first identified in rat brain that has antioxidant and free radical scavenging activities in several experimental models; may be measured in plasma as an index of melatonin synthesis and...

AFMK

Reference: 10005254-5

€0.00 (tax incl.)

A melatonin metabolite first identified in rat brain that has antioxidant and free radical scavenging activities in several experimental models; may be measured in plasma as an index of melatonin synthesis and...

AFMK

Reference: 10005254-50

€0.00 (tax incl.)

A melatonin metabolite first identified in rat brain that has antioxidant and free radical scavenging activities in several experimental models; may be measured in plasma as an index of melatonin synthesis and...

TOFA

Reference: 10005263-10

€0.00 (tax incl.)

An inhibitor of fatty acid synthesis that blocks the synthesis of malonyl-CoA by acetyl-CoA carboxylase (ACC)

TOFA

Reference: 10005263-100

€0.00 (tax incl.)

An inhibitor of fatty acid synthesis that blocks the synthesis of malonyl-CoA by acetyl-CoA carboxylase (ACC)

TOFA

Reference: 10005263-5

€0.00 (tax incl.)

An inhibitor of fatty acid synthesis that blocks the synthesis of malonyl-CoA by acetyl-CoA carboxylase (ACC)

TOFA

Reference: 10005263-50

€0.00 (tax incl.)

An inhibitor of fatty acid synthesis that blocks the synthesis of malonyl-CoA by acetyl-CoA carboxylase (ACC)

(±)-C75

Reference: 10005270-1

€0.00 (tax incl.)

A stable inhibitor of FASN that leads to profound weight loss and feeding inhibition in both high-fat diet wild type obese and leptin-deficient ob/ob mice

(±)-C75

Reference: 10005270-10

€0.00 (tax incl.)

A stable inhibitor of FASN that leads to profound weight loss and feeding inhibition in both high-fat diet wild type obese and leptin-deficient ob/ob mice

(±)-C75

Reference: 10005270-5

€0.00 (tax incl.)

A stable inhibitor of FASN that leads to profound weight loss and feeding inhibition in both high-fat diet wild type obese and leptin-deficient ob/ob mice

Category: Reagents

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