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(+)-trans-C75 (+)-trans-C75

(+)-trans-C75

Reference: 9000783-5
€0.00 (tax incl.)
An enantiomer of C75, which in racemic form is a stable FASN inhibitor that when administered leads to profound weight loss and feeding inhibition in both high-fat diet wild type obese and leptin-deficient ob/ob mice
(−)-trans-C75 (−)-trans-C75

(−)-trans-C75

Reference: 9000784-1
€0.00 (tax incl.)
An enantiomer of C75, which in racemic form is a stable FASN inhibitor that when administered leads to profound weight loss and feeding inhibition in both high-fat diet wild type obese and leptin-deficient ob/ob mice
(−)-trans-C75 (−)-trans-C75

(−)-trans-C75

Reference: 9000784-10
€0.00 (tax incl.)
An enantiomer of C75, which in racemic form is a stable FASN inhibitor that when administered leads to profound weight loss and feeding inhibition in both high-fat diet wild type obese and leptin-deficient ob/ob mice
(−)-trans-C75 (−)-trans-C75

(−)-trans-C75

Reference: 9000784-5
€0.00 (tax incl.)
An enantiomer of C75, which in racemic form is a stable FASN inhibitor that when administered leads to profound weight loss and feeding inhibition in both high-fat diet wild type obese and leptin-deficient ob/ob mice
3-Deazaadenosine 3-Deazaadenosine

3-Deazaadenosine

Reference: 9000785-1
€0.00 (tax incl.)
An inhibitor of SAH hydrolase (Ki = 3.9 μM); has anti-inflammatory, antiviral, and antibacterial activities
3-Deazaadenosine 3-Deazaadenosine

3-Deazaadenosine

Reference: 9000785-10
€0.00 (tax incl.)
An inhibitor of SAH hydrolase (Ki = 3.9 μM); has anti-inflammatory, antiviral, and antibacterial activities
3-Deazaadenosine 3-Deazaadenosine

3-Deazaadenosine

Reference: 9000785-5
€0.00 (tax incl.)
An inhibitor of SAH hydrolase (Ki = 3.9 μM); has anti-inflammatory, antiviral, and antibacterial activities
3-Deaza-2'-deoxyadenosine 3-Deaza-2'-deoxyadenosine

3-Deaza-2'-deoxyadenosine

Reference: 9000786-1
€0.00 (tax incl.)
Strongly inhibits lymphocyte-mediated cytolysis with low cytotoxicity when applied at 100 μM; can also be used to evaluate the role of the adenine N3 nitrogen in DNA structure and function
3-Deaza-2'-deoxyadenosine 3-Deaza-2'-deoxyadenosine

3-Deaza-2'-deoxyadenosine

Reference: 9000786-10
€0.00 (tax incl.)
Strongly inhibits lymphocyte-mediated cytolysis with low cytotoxicity when applied at 100 μM; can also be used to evaluate the role of the adenine N3 nitrogen in DNA structure and function
3-Deaza-2'-deoxyadenosine 3-Deaza-2'-deoxyadenosine

3-Deaza-2'-deoxyadenosine

Reference: 9000786-25
€0.00 (tax incl.)
Strongly inhibits lymphocyte-mediated cytolysis with low cytotoxicity when applied at 100 μM; can also be used to evaluate the role of the adenine N3 nitrogen in DNA structure and function
3-Deaza-2'-deoxyadenosine 3-Deaza-2'-deoxyadenosine

3-Deaza-2'-deoxyadenosine

Reference: 9000786-5
€0.00 (tax incl.)
Strongly inhibits lymphocyte-mediated cytolysis with low cytotoxicity when applied at 100 μM; can also be used to evaluate the role of the adenine N3 nitrogen in DNA structure and function
2-chloro-3-Deazaadenosine 2-chloro-3-Deazaadenosine

2-chloro-3-Deazaadenosine

Reference: 9000787-1
€0.00 (tax incl.)
A stable analog of adenosine that acts as an agonist for adenosine receptors (Ki = 0.3, 0.08, 25.5, and 1.9 μM for A1, A2A, A2B, and A3 receptors, respectively); modulates neurotransmission release and blocks seizures...
2-chloro-3-Deazaadenosine 2-chloro-3-Deazaadenosine

2-chloro-3-Deazaadenosine

Reference: 9000787-10
€0.00 (tax incl.)
A stable analog of adenosine that acts as an agonist for adenosine receptors (Ki = 0.3, 0.08, 25.5, and 1.9 μM for A1, A2A, A2B, and A3 receptors, respectively); modulates neurotransmission release and blocks seizures...
2-chloro-3-Deazaadenosine 2-chloro-3-Deazaadenosine

2-chloro-3-Deazaadenosine

Reference: 9000787-5
€0.00 (tax incl.)
A stable analog of adenosine that acts as an agonist for adenosine receptors (Ki = 0.3, 0.08, 25.5, and 1.9 μM for A1, A2A, A2B, and A3 receptors, respectively); modulates neurotransmission release and blocks seizures...
KN-92 (hydrochloride) KN-92 (hydrochloride)

KN-92 (hydrochloride)

Reference: 9000890-1
€0.00 (tax incl.)
An inactive derivative of KN-93, the selective inhibitor of CaMKII; ineffective at inhibiting CaMKII or arresting cell growth of NIH 3T3 fibroblasts at concentrations up to 25 μM
KN-92 (hydrochloride) KN-92 (hydrochloride)

KN-92 (hydrochloride)

Reference: 9000890-10
€0.00 (tax incl.)
An inactive derivative of KN-93, the selective inhibitor of CaMKII; ineffective at inhibiting CaMKII or arresting cell growth of NIH 3T3 fibroblasts at concentrations up to 25 μM
KN-92 (hydrochloride) KN-92 (hydrochloride)

KN-92 (hydrochloride)

Reference: 9000890-5
€0.00 (tax incl.)
An inactive derivative of KN-93, the selective inhibitor of CaMKII; ineffective at inhibiting CaMKII or arresting cell growth of NIH 3T3 fibroblasts at concentrations up to 25 μM
Progesterone-3-biotinyl Photoaffinity Probe Progesterone-3-biotinyl Photoaffinity Probe

Progesterone-3-biotinyl Photoaffinity Probe

Reference: 9000891-1
€0.00 (tax incl.)
A photoaffinity probe that consists of active progesterone, a diazirine-UV (312 nm)-sensitive moiety, and a biotin tag; can be used to detect and observe the interaction of progesterone with target proteins
Progesterone-3-biotinyl Photoaffinity Probe Progesterone-3-biotinyl Photoaffinity Probe

Progesterone-3-biotinyl Photoaffinity Probe

Reference: 9000891-5
€0.00 (tax incl.)
A photoaffinity probe that consists of active progesterone, a diazirine-UV (312 nm)-sensitive moiety, and a biotin tag; can be used to detect and observe the interaction of progesterone with target proteins
Progesterone-3-biotinyl Photoaffinity Probe Progesterone-3-biotinyl Photoaffinity Probe

Progesterone-3-biotinyl Photoaffinity Probe

Reference: 9000891-500
€0.00 (tax incl.)
A photoaffinity probe that consists of active progesterone, a diazirine-UV (312 nm)-sensitive moiety, and a biotin tag; can be used to detect and observe the interaction of progesterone with target proteins
Arachidonoyl-L-carnitine (chloride) Arachidonoyl-L-carnitine (chloride)

Arachidonoyl-L-carnitine (chloride)

Reference: 9000939-10
€0.00 (tax incl.)
An acylcarnitine formed from carnitine conjugated to arachidonic acid; may be useful as a marker of mitochondrial dysfunction
Arachidonoyl-L-carnitine (chloride) Arachidonoyl-L-carnitine (chloride)

Arachidonoyl-L-carnitine (chloride)

Reference: 9000939-25
€0.00 (tax incl.)
An acylcarnitine formed from carnitine conjugated to arachidonic acid; may be useful as a marker of mitochondrial dysfunction
Arachidonoyl-L-carnitine (chloride) Arachidonoyl-L-carnitine (chloride)

Arachidonoyl-L-carnitine (chloride)

Reference: 9000939-50
€0.00 (tax incl.)
An acylcarnitine formed from carnitine conjugated to arachidonic acid; may be useful as a marker of mitochondrial dysfunction
Vigabatrin Vigabatrin

Vigabatrin

Reference: 9000976-10
€0.00 (tax incl.)
A structural analog of the inhibitory neurotransmitter GABA that irreversibly inhibits its catabolism by GABA transaminase; produces a dose-dependent increase in extracellular GABA, and has been shown to result in...
Vigabatrin Vigabatrin

Vigabatrin

Reference: 9000976-25
€0.00 (tax incl.)
A structural analog of the inhibitory neurotransmitter GABA that irreversibly inhibits its catabolism by GABA transaminase; produces a dose-dependent increase in extracellular GABA, and has been shown to result in...
Vigabatrin Vigabatrin

Vigabatrin

Reference: 9000976-5
€0.00 (tax incl.)
A structural analog of the inhibitory neurotransmitter GABA that irreversibly inhibits its catabolism by GABA transaminase; produces a dose-dependent increase in extracellular GABA, and has been shown to result in...
Vigabatrin Vigabatrin

Vigabatrin

Reference: 9000976-50
€0.00 (tax incl.)
A structural analog of the inhibitory neurotransmitter GABA that irreversibly inhibits its catabolism by GABA transaminase; produces a dose-dependent increase in extracellular GABA, and has been shown to result in...
AS-605240 (potassium salt) AS-605240 (potassium salt)

AS-605240 (potassium salt)

Reference: 9000980-1
€0.00 (tax incl.)
An orally active inhibitor of PI3-kinase γ that suppresses joint inflammation in mouse models of rheumatoid arthritis; inhibits human recombinant PI3Kγ, α, β, and δ in an ATP-competitive manner with IC50 values of 8,...
AS-605240 (potassium salt) AS-605240 (potassium salt)

AS-605240 (potassium salt)

Reference: 9000980-10
€0.00 (tax incl.)
An orally active inhibitor of PI3-kinase γ that suppresses joint inflammation in mouse models of rheumatoid arthritis; inhibits human recombinant PI3Kγ, α, β, and δ in an ATP-competitive manner with IC50 values of 8,...
AS-605240 (potassium salt) AS-605240 (potassium salt)

AS-605240 (potassium salt)

Reference: 9000980-25
€0.00 (tax incl.)
An orally active inhibitor of PI3-kinase γ that suppresses joint inflammation in mouse models of rheumatoid arthritis; inhibits human recombinant PI3Kγ, α, β, and δ in an ATP-competitive manner with IC50 values of 8,...
AS-605240 (potassium salt) AS-605240 (potassium salt)

AS-605240 (potassium salt)

Reference: 9000980-5
€0.00 (tax incl.)
An orally active inhibitor of PI3-kinase γ that suppresses joint inflammation in mouse models of rheumatoid arthritis; inhibits human recombinant PI3Kγ, α, β, and δ in an ATP-competitive manner with IC50 values of 8,...
PD 166326 PD 166326

PD 166326

Reference: 9000988-1
€0.00 (tax incl.)
A pyridopyrimidine-type inhibitor of receptor tyrosine kinases that inhibits c-abl (IC50 = 8 nM) and Bcr/Abl-dependent cell growth (IC50 = 0.4 nM); also potently inhibits c-src (IC50 = 6 nM); effectively blocks...
PD 166326 PD 166326

PD 166326

Reference: 9000988-10
€0.00 (tax incl.)
A pyridopyrimidine-type inhibitor of receptor tyrosine kinases that inhibits c-abl (IC50 = 8 nM) and Bcr/Abl-dependent cell growth (IC50 = 0.4 nM); also potently inhibits c-src (IC50 = 6 nM); effectively blocks...
PD 166326 PD 166326

PD 166326

Reference: 9000988-5
€0.00 (tax incl.)
A pyridopyrimidine-type inhibitor of receptor tyrosine kinases that inhibits c-abl (IC50 = 8 nM) and Bcr/Abl-dependent cell growth (IC50 = 0.4 nM); also potently inhibits c-src (IC50 = 6 nM); effectively blocks...
N-3-hydroxydecanoyl-L-Homoserine lactone N-3-hydroxydecanoyl-L-Homoserine lactone

N-3-hydroxydecanoyl-L-Homoserine lactone

Reference: 9001147-1
€0.00 (tax incl.)
A small diffusible signaling molecule secreted by various bacteria; produced via lactonolysis from 3-oxodecanoyl-homoserine lactone
N-3-hydroxydecanoyl-L-Homoserine lactone N-3-hydroxydecanoyl-L-Homoserine lactone

N-3-hydroxydecanoyl-L-Homoserine lactone

Reference: 9001147-10
€0.00 (tax incl.)
A small diffusible signaling molecule secreted by various bacteria; produced via lactonolysis from 3-oxodecanoyl-homoserine lactone
N-3-hydroxydecanoyl-L-Homoserine lactone N-3-hydroxydecanoyl-L-Homoserine lactone

N-3-hydroxydecanoyl-L-Homoserine lactone

Reference: 9001147-5
€0.00 (tax incl.)
A small diffusible signaling molecule secreted by various bacteria; produced via lactonolysis from 3-oxodecanoyl-homoserine lactone
Ketorolac Ketorolac

Ketorolac

Reference: 9001148-1
€0.00 (tax incl.)
An NSAID and COX inhibitor (IC50s = 20 nM for both COX-1 and COX-2); prevents increases in paw swelling, increases paw withdrawal latency in a hot-plate test, and decreases PGE2 levels in paw tissue in a mouse model...
Ketorolac Ketorolac

Ketorolac

Reference: 9001148-100
€0.00 (tax incl.)
An NSAID and COX inhibitor (IC50s = 20 nM for both COX-1 and COX-2); prevents increases in paw swelling, increases paw withdrawal latency in a hot-plate test, and decreases PGE2 levels in paw tissue in a mouse model...
Ketorolac Ketorolac

Ketorolac

Reference: 9001148-50
€0.00 (tax incl.)
An NSAID and COX inhibitor (IC50s = 20 nM for both COX-1 and COX-2); prevents increases in paw swelling, increases paw withdrawal latency in a hot-plate test, and decreases PGE2 levels in paw tissue in a mouse model...
Ketorolac Ketorolac

Ketorolac

Reference: 9001148-500
€0.00 (tax incl.)
An NSAID and COX inhibitor (IC50s = 20 nM for both COX-1 and COX-2); prevents increases in paw swelling, increases paw withdrawal latency in a hot-plate test, and decreases PGE2 levels in paw tissue in a mouse model...
N-3-hydroxyoctanoyl-L-Homoserine lactone N-3-hydroxyoctanoyl-L-Homoserine lactone

N-3-hydroxyoctanoyl-L-Homoserine lactone

Reference: 9001150-1
€0.00 (tax incl.)
A small diffusible signaling molecule secreted by various bacteria; can have activating or suppressing effects on gene expression and biofilm formation, respectively; produced via lactonolysis from...
N-3-hydroxyoctanoyl-L-Homoserine lactone N-3-hydroxyoctanoyl-L-Homoserine lactone

N-3-hydroxyoctanoyl-L-Homoserine lactone

Reference: 9001150-10
€0.00 (tax incl.)
A small diffusible signaling molecule secreted by various bacteria; can have activating or suppressing effects on gene expression and biofilm formation, respectively; produced via lactonolysis from...
N-3-hydroxyoctanoyl-L-Homoserine lactone N-3-hydroxyoctanoyl-L-Homoserine lactone

N-3-hydroxyoctanoyl-L-Homoserine lactone

Reference: 9001150-25
€0.00 (tax incl.)
A small diffusible signaling molecule secreted by various bacteria; can have activating or suppressing effects on gene expression and biofilm formation, respectively; produced via lactonolysis from...
N-3-hydroxyoctanoyl-L-Homoserine lactone N-3-hydroxyoctanoyl-L-Homoserine lactone

N-3-hydroxyoctanoyl-L-Homoserine lactone

Reference: 9001150-5
€0.00 (tax incl.)
A small diffusible signaling molecule secreted by various bacteria; can have activating or suppressing effects on gene expression and biofilm formation, respectively; produced via lactonolysis from...
Piperlonguminine Piperlonguminine

Piperlonguminine

Reference: 9001155-10
€0.00 (tax incl.)
An alkaloid amide from species of the genus Piper, a plant used in traditional medicine that demonstrates antifungal, anticancer, antihyperlipidemic, and anti-inflammatory properties
Piperlonguminine Piperlonguminine

Piperlonguminine

Reference: 9001155-25
€0.00 (tax incl.)
An alkaloid amide from species of the genus Piper, a plant used in traditional medicine that demonstrates antifungal, anticancer, antihyperlipidemic, and anti-inflammatory properties
Piperlonguminine Piperlonguminine

Piperlonguminine

Reference: 9001155-5
€0.00 (tax incl.)
An alkaloid amide from species of the genus Piper, a plant used in traditional medicine that demonstrates antifungal, anticancer, antihyperlipidemic, and anti-inflammatory properties
Piperlonguminine Piperlonguminine

Piperlonguminine

Reference: 9001155-50
€0.00 (tax incl.)
An alkaloid amide from species of the genus Piper, a plant used in traditional medicine that demonstrates antifungal, anticancer, antihyperlipidemic, and anti-inflammatory properties
Atipamezole (hydrochloride) Atipamezole (hydrochloride)

Atipamezole (hydrochloride)

Reference: 9001181-10
€0.00 (tax incl.)
An imidazole that potently antagonizes the α2-adrenoceptor (Ki = 1.6 nM); shows selectivity over the α1-adrenoceptor (Ki = 13,300 nM) and is a poor antagonist at a wide variety of other receptors and channels
Atipamezole (hydrochloride) Atipamezole (hydrochloride)

Atipamezole (hydrochloride)

Reference: 9001181-25
€0.00 (tax incl.)
An imidazole that potently antagonizes the α2-adrenoceptor (Ki = 1.6 nM); shows selectivity over the α1-adrenoceptor (Ki = 13,300 nM) and is a poor antagonist at a wide variety of other receptors and channels
Atipamezole (hydrochloride) Atipamezole (hydrochloride)

Atipamezole (hydrochloride)

Reference: 9001181-5
€0.00 (tax incl.)
An imidazole that potently antagonizes the α2-adrenoceptor (Ki = 1.6 nM); shows selectivity over the α1-adrenoceptor (Ki = 13,300 nM) and is a poor antagonist at a wide variety of other receptors and channels
Atipamezole (hydrochloride) Atipamezole (hydrochloride)

Atipamezole (hydrochloride)

Reference: 9001181-50
€0.00 (tax incl.)
An imidazole that potently antagonizes the α2-adrenoceptor (Ki = 1.6 nM); shows selectivity over the α1-adrenoceptor (Ki = 13,300 nM) and is a poor antagonist at a wide variety of other receptors and channels
Nat-20(S)-yne Nat-20(S)-yne

Nat-20(S)-yne

Reference: 9001369-1
€0.00 (tax incl.)
A form of nat-20(S)-OHC with a terminal alkyne group, which can be used in linking reactions known as click chemistry; has been conjugated with magnetic beads to demonstrate that nat-20(S)-OHC directly binds SMO
Nat-20(S)-yne Nat-20(S)-yne

Nat-20(S)-yne

Reference: 9001369-10
€0.00 (tax incl.)
A form of nat-20(S)-OHC with a terminal alkyne group, which can be used in linking reactions known as click chemistry; has been conjugated with magnetic beads to demonstrate that nat-20(S)-OHC directly binds SMO
Nat-20(S)-yne Nat-20(S)-yne

Nat-20(S)-yne

Reference: 9001369-25
€0.00 (tax incl.)
A form of nat-20(S)-OHC with a terminal alkyne group, which can be used in linking reactions known as click chemistry; has been conjugated with magnetic beads to demonstrate that nat-20(S)-OHC directly binds SMO
Nat-20(S)-yne Nat-20(S)-yne

Nat-20(S)-yne

Reference: 9001369-5
€0.00 (tax incl.)
A form of nat-20(S)-OHC with a terminal alkyne group, which can be used in linking reactions known as click chemistry; has been conjugated with magnetic beads to demonstrate that nat-20(S)-OHC directly binds SMO
N-Acetyltyramine N-Acetyltyramine

N-Acetyltyramine

Reference: 9001373-25
€0.00 (tax incl.)
A tyramine metabolite; enhances cytotoxicity of doxorubicin in resistant P388 murine leukemia cells (IC50s = 0.13 and 0.48 μg/ml for doxorubicin plus N-acetyltyramine and doxorubicin alone, respectively)
N-Acetyltyramine N-Acetyltyramine

N-Acetyltyramine

Reference: 9001373-5
€0.00 (tax incl.)
A tyramine metabolite; enhances cytotoxicity of doxorubicin in resistant P388 murine leukemia cells (IC50s = 0.13 and 0.48 μg/ml for doxorubicin plus N-acetyltyramine and doxorubicin alone, respectively)
CAY10679 CAY10679

CAY10679

Reference: 9001475-10
€0.00 (tax incl.)
An anionic oligopeptide-based bola-amphiphile that contains a hexane moiety flanked by a glycylglycine group at each end, which creates distinct hydrophilic and hydrophobic regions
CAY10679 CAY10679

CAY10679

Reference: 9001475-100
€0.00 (tax incl.)
An anionic oligopeptide-based bola-amphiphile that contains a hexane moiety flanked by a glycylglycine group at each end, which creates distinct hydrophilic and hydrophobic regions
CAY10679 CAY10679

CAY10679

Reference: 9001475-25
€0.00 (tax incl.)
An anionic oligopeptide-based bola-amphiphile that contains a hexane moiety flanked by a glycylglycine group at each end, which creates distinct hydrophilic and hydrophobic regions
CAY10679 CAY10679

CAY10679

Reference: 9001475-50
€0.00 (tax incl.)
An anionic oligopeptide-based bola-amphiphile that contains a hexane moiety flanked by a glycylglycine group at each end, which creates distinct hydrophilic and hydrophobic regions
Nanaomycin A Nanaomycin A

Nanaomycin A

Reference: 9001479-5
€0.00 (tax incl.)
A quinone bacterial metabolite; inhibits the growth of a variety of bacteria (MICs = P. falciparum (IC80 = 0.0033 µM); inhibits proliferation of HCT116, A549, and HL-60 cancer cells (IC50s = 0.4, 4.1, and 0.8 µM,...
4-methyl Erlotinib 4-methyl Erlotinib

4-methyl Erlotinib

Reference: 9001510-1
€0.00 (tax incl.)
An erlotinib analog characterized by the addition of a methyl group at the four position of the phenyl group
4-methyl Erlotinib 4-methyl Erlotinib

4-methyl Erlotinib

Reference: 9001510-10
€0.00 (tax incl.)
An erlotinib analog characterized by the addition of a methyl group at the four position of the phenyl group
4-methyl Erlotinib 4-methyl Erlotinib

4-methyl Erlotinib

Reference: 9001510-5
€0.00 (tax incl.)
An erlotinib analog characterized by the addition of a methyl group at the four position of the phenyl group
β-Tocotrienol β-Tocotrienol

β-Tocotrienol

Reference: 9001533-1
€0.00 (tax incl.)
An isomer of Vitamin E that has less potent antioxidant properties than α-tocotrienol
β-Tocotrienol β-Tocotrienol

β-Tocotrienol

Reference: 9001533-10
€0.00 (tax incl.)
An isomer of Vitamin E that has less potent antioxidant properties than α-tocotrienol
β-Tocotrienol β-Tocotrienol

β-Tocotrienol

Reference: 9001533-25
€0.00 (tax incl.)
An isomer of Vitamin E that has less potent antioxidant properties than α-tocotrienol
β-Tocotrienol β-Tocotrienol

β-Tocotrienol

Reference: 9001533-5
€0.00 (tax incl.)
An isomer of Vitamin E that has less potent antioxidant properties than α-tocotrienol
N1-Acetylspermidine (hydrochloride) N1-Acetylspermidine (hydrochloride)

N1-Acetylspermidine (hydrochloride)

Reference: 9001535-1
€0.00 (tax incl.)
A substrate for polyamine oxidase that is oxidized to 3-acetamidopropanal and putrescine, a polyamine involved in the division, differentiation, and membrane function of cells; used to examine the interaction between...
N1-Acetylspermidine (hydrochloride) N1-Acetylspermidine (hydrochloride)

N1-Acetylspermidine (hydrochloride)

Reference: 9001535-10
€0.00 (tax incl.)
A substrate for polyamine oxidase that is oxidized to 3-acetamidopropanal and putrescine, a polyamine involved in the division, differentiation, and membrane function of cells; used to examine the interaction between...
N1-Acetylspermidine (hydrochloride) N1-Acetylspermidine (hydrochloride)

N1-Acetylspermidine (hydrochloride)

Reference: 9001535-5
€0.00 (tax incl.)
A substrate for polyamine oxidase that is oxidized to 3-acetamidopropanal and putrescine, a polyamine involved in the division, differentiation, and membrane function of cells; used to examine the interaction between...
Deltarasin (hydrochloride) Deltarasin (hydrochloride)

Deltarasin (hydrochloride)

Reference: 9001536-1
€0.00 (tax incl.)
A small molecule that binds to the farnesyl-binding pocket of PDEδ (Kd = 41 nM) in cells thus inhibiting its interaction with KRAS and disrupting RAS signaling; reduces proliferation and increases cell death of...
Deltarasin (hydrochloride) Deltarasin (hydrochloride)

Deltarasin (hydrochloride)

Reference: 9001536-10
€0.00 (tax incl.)
A small molecule that binds to the farnesyl-binding pocket of PDEδ (Kd = 41 nM) in cells thus inhibiting its interaction with KRAS and disrupting RAS signaling; reduces proliferation and increases cell death of...
Deltarasin (hydrochloride) Deltarasin (hydrochloride)

Deltarasin (hydrochloride)

Reference: 9001536-5
€0.00 (tax incl.)
A small molecule that binds to the farnesyl-binding pocket of PDEδ (Kd = 41 nM) in cells thus inhibiting its interaction with KRAS and disrupting RAS signaling; reduces proliferation and increases cell death of...
Salvianolic Acid B Salvianolic Acid B

Salvianolic Acid B

Reference: 9001577-1
€0.00 (tax incl.)
An antioxidant and free radical scavenging compound extracted from S. miltiorrhiza that has been investigated for its cardioprotective and chemopreventative properties
Salvianolic Acid B Salvianolic Acid B

Salvianolic Acid B

Reference: 9001577-10
€0.00 (tax incl.)
An antioxidant and free radical scavenging compound extracted from S. miltiorrhiza that has been investigated for its cardioprotective and chemopreventative properties
Salvianolic Acid B Salvianolic Acid B

Salvianolic Acid B

Reference: 9001577-25
€0.00 (tax incl.)
An antioxidant and free radical scavenging compound extracted from S. miltiorrhiza that has been investigated for its cardioprotective and chemopreventative properties
Salvianolic Acid B Salvianolic Acid B

Salvianolic Acid B

Reference: 9001577-5
€0.00 (tax incl.)
An antioxidant and free radical scavenging compound extracted from S. miltiorrhiza that has been investigated for its cardioprotective and chemopreventative properties
APY0201 APY0201

APY0201

Reference: 9001589-1
€0.00 (tax incl.)
An inhibitor of PIKFYVE (IC50 = 5.2 nM); selectively inhibits IL-12 family inflammatory cytokine production (IC50s = 8, 99, and >10,000 nM for IL-12p70, IL-12p40, and TNF-α in stimulated human PBMCs); selective for...
APY0201 APY0201

APY0201

Reference: 9001589-10
€0.00 (tax incl.)
An inhibitor of PIKFYVE (IC50 = 5.2 nM); selectively inhibits IL-12 family inflammatory cytokine production (IC50s = 8, 99, and >10,000 nM for IL-12p70, IL-12p40, and TNF-α in stimulated human PBMCs); selective for...
APY0201 APY0201

APY0201

Reference: 9001589-25
€0.00 (tax incl.)
An inhibitor of PIKFYVE (IC50 = 5.2 nM); selectively inhibits IL-12 family inflammatory cytokine production (IC50s = 8, 99, and >10,000 nM for IL-12p70, IL-12p40, and TNF-α in stimulated human PBMCs); selective for...
APY0201 APY0201

APY0201

Reference: 9001589-5
€0.00 (tax incl.)
An inhibitor of PIKFYVE (IC50 = 5.2 nM); selectively inhibits IL-12 family inflammatory cytokine production (IC50s = 8, 99, and >10,000 nM for IL-12p70, IL-12p40, and TNF-α in stimulated human PBMCs); selective for...
N-phenylacetyl-L-Homoserine lactone N-phenylacetyl-L-Homoserine lactone

N-phenylacetyl-L-Homoserine lactone

Reference: 9001737-1
€0.00 (tax incl.)
A small diffusible signaling molecule involved in quorum sensing in the model symbiont V. fischeri and the pathogens A. tumefaciens and P. aeruginosa
N-phenylacetyl-L-Homoserine lactone N-phenylacetyl-L-Homoserine lactone

N-phenylacetyl-L-Homoserine lactone

Reference: 9001737-10
€0.00 (tax incl.)
A small diffusible signaling molecule involved in quorum sensing in the model symbiont V. fischeri and the pathogens A. tumefaciens and P. aeruginosa
N-phenylacetyl-L-Homoserine lactone N-phenylacetyl-L-Homoserine lactone

N-phenylacetyl-L-Homoserine lactone

Reference: 9001737-25
€0.00 (tax incl.)
A small diffusible signaling molecule involved in quorum sensing in the model symbiont V. fischeri and the pathogens A. tumefaciens and P. aeruginosa
N-phenylacetyl-L-Homoserine lactone N-phenylacetyl-L-Homoserine lactone

N-phenylacetyl-L-Homoserine lactone

Reference: 9001737-5
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A small diffusible signaling molecule involved in quorum sensing in the model symbiont V. fischeri and the pathogens A. tumefaciens and P. aeruginosa
A 83-01 A 83-01

A 83-01

Reference: 9001799-1
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An inhibitor of ALK5, ALK4, and ALK7 (IC50s = 12, 45, and 7.5 nM, respectively); blocks the phosphorylation of SMAD2/3 and inhibits TGF-β-induced epithelial-to-mesenchymal transition; used to reprogram fibroblasts...

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