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1437732 Item(s)

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  2. 27
  3. 28
  4. 29
  5. 30
Name PDF Type Clone Specific against Appl. Host Item no. Amount ✓ Price
Elacestrant Chemicals Other Elacestrant (RAD-1901) is a novel, orally bioavailable small-molecule selective estrogen receptor degrader (SERD). DCC-DC70104-100mg

DCChemicals 		100 mg Login
Compare
Elacestrant Chemicals Other Elacestrant (RAD-1901) is a novel, orally bioavailable small-molecule selective estrogen receptor degrader (SERD). DCC-DC70104-250mg

DCChemicals 		250 mg Login
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Elacestrant Chemicals Other Elacestrant (RAD-1901) is a novel, orally bioavailable small-molecule selective estrogen receptor degrader (SERD). DCC-DC70104-1g

DCChemicals 		1 g Login
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AC1-­IN-­38 Chemicals Other other DCC-DC70169-100mg

DCChemicals 		100 mg Login
Compare
AC1-­IN-­38 Chemicals Other other DCC-DC70169-250mg

DCChemicals 		250 mg Login
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AC1-­IN-­38 Chemicals Other other DCC-DC70169-1g

DCChemicals 		1 g Login
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FGIN-­1-­27 Chemicals Other FGIN-1-27 is an anxiolytic compound that acts as a selective agonist at the peripheral benzodiazepine receptor (TSPO).FGIN-1-27 inhibited Th17 cell differentiation, significantly downregulated the expression of RORγt target genes, notably Il17a, Il17f, Il23r, Ltb4r1, Ccr6.FGIN-1-27 protected mice against EAE, induced amino acid starvation response (AAR), FGIN-1-27 produced anti-anxiety and anti-panic effects in non-mammalian models. DCC-DC70409-100mg

DCChemicals 		100 mg Login
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FGIN-­1-­27 Chemicals Other FGIN-1-27 is an anxiolytic compound that acts as a selective agonist at the peripheral benzodiazepine receptor (TSPO).FGIN-1-27 inhibited Th17 cell differentiation, significantly downregulated the expression of RORγt target genes, notably Il17a, Il17f, Il23r, Ltb4r1, Ccr6.FGIN-1-27 protected mice against EAE, induced amino acid starvation response (AAR), FGIN-1-27 produced anti-anxiety and anti-panic effects in non-mammalian models. DCC-DC70409-250mg

DCChemicals 		250 mg Login
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Bemcentinib（R428，BGB324) Inhibitors Other DCC-DC7258-250mg

DCChemicals 		250 mg Login
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Bemcentinib（R428，BGB324) Inhibitors Other DCC-DC7258-1g

DCChemicals 		1 g Login
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Resminostat hydrochloride (4SC-­201) Inhibitors Other DCC-DC7261-100mg

DCChemicals 		100 mg Login
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Resminostat hydrochloride (4SC-­201) Inhibitors Other DCC-DC7261-250mg

DCChemicals 		250 mg Login
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Resminostat hydrochloride (4SC-­201) Inhibitors Other DCC-DC7261-1g

DCChemicals 		1 g Login
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LCS3 Chemicals Other LCS3 inhibits glutathione disulfide reductase (GSR) and thioredoxin reductase 1 (TXNRD1) (IC50=3.3 µM and 3.8 µM, respectively) synergistically. LCS3 shows anti-tumor activity, and induces apoptosis. LCS3 can be used in lung adenocarcinoma (LUAD) research. DCC-DC71723-100mg

DCChemicals 		100 mg Login
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LCS3 Chemicals Other LCS3 inhibits glutathione disulfide reductase (GSR) and thioredoxin reductase 1 (TXNRD1) (IC50=3.3 µM and 3.8 µM, respectively) synergistically. LCS3 shows anti-tumor activity, and induces apoptosis. LCS3 can be used in lung adenocarcinoma (LUAD) research. DCC-DC71723-250mg

DCChemicals 		250 mg Login
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LCS3 Chemicals Other LCS3 inhibits glutathione disulfide reductase (GSR) and thioredoxin reductase 1 (TXNRD1) (IC50=3.3 µM and 3.8 µM, respectively) synergistically. LCS3 shows anti-tumor activity, and induces apoptosis. LCS3 can be used in lung adenocarcinoma (LUAD) research. DCC-DC71723-1g

DCChemicals 		1 g Login
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LDCA Chemicals Other LDCA is a dual-hit metabolic modulator and inhibits LDH-A enzyme activity to stimulate apoptosis in the malignant population. LDCA can be used for the research of oncogenic progression. DCC-DC71724-100mg

DCChemicals 		100 mg Login
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LDCA Chemicals Other LDCA is a dual-hit metabolic modulator and inhibits LDH-A enzyme activity to stimulate apoptosis in the malignant population. LDCA can be used for the research of oncogenic progression. DCC-DC71724-250mg

DCChemicals 		250 mg Login
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LDCA Chemicals Other LDCA is a dual-hit metabolic modulator and inhibits LDH-A enzyme activity to stimulate apoptosis in the malignant population. LDCA can be used for the research of oncogenic progression. DCC-DC71724-1g

DCChemicals 		1 g Login
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GLN-­1062 Chemicals Other GLN-1062 (Memogain) is an inactive pro-drug of galantamine, the latter being a plant alkaloid approved for the treatment of mild to moderate Alzheimer's disease. DCC-DC71898-100mg

DCChemicals 		100 mg Login
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GLN-­1062 Chemicals Other GLN-1062 (Memogain) is an inactive pro-drug of galantamine, the latter being a plant alkaloid approved for the treatment of mild to moderate Alzheimer's disease. DCC-DC71898-250mg

DCChemicals 		250 mg Login
Compare
GLN-­1062 Chemicals Other GLN-1062 (Memogain) is an inactive pro-drug of galantamine, the latter being a plant alkaloid approved for the treatment of mild to moderate Alzheimer's disease. DCC-DC71898-1g

DCChemicals 		1 g Login
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WAY-­296817 Chemicals Other WAY-296817 is casein kinase 1 (CK1) inhibitor and can be used for research on the treatment or prevention. DCC-DC71902-100mg

DCChemicals 		100 mg Login
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WAY-­296817 Chemicals Other WAY-296817 is casein kinase 1 (CK1) inhibitor and can be used for research on the treatment or prevention. DCC-DC71902-250mg

DCChemicals 		250 mg Login
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WAY-­296817 Chemicals Other WAY-296817 is casein kinase 1 (CK1) inhibitor and can be used for research on the treatment or prevention. DCC-DC71902-1g

DCChemicals 		1 g Login
Compare
Name Price
Elacestrant Login Elacestrant
Type Chemicals
Clone
Specific against Other
Appl. Elacestrant (RAD-1901) is a novel, orally bioavailable small-molecule selective estrogen receptor degrader (SERD).
Host
Item no.
Amount 100 mg
Available
Elacestrant Login Elacestrant
Type Chemicals
Clone
Specific against Other
Appl. Elacestrant (RAD-1901) is a novel, orally bioavailable small-molecule selective estrogen receptor degrader (SERD).
Host
Item no.
Amount 250 mg
Available
Elacestrant Login Elacestrant
Type Chemicals
Clone
Specific against Other
Appl. Elacestrant (RAD-1901) is a novel, orally bioavailable small-molecule selective estrogen receptor degrader (SERD).
Host
Item no.
Amount 1 g
Available
AC1-­IN-­38 Login AC1-IN-38
Type Chemicals
Clone
Specific against Other
Appl. other
Host
Item no.
Amount 100 mg
Available
AC1-­IN-­38 Login AC1-IN-38
Type Chemicals
Clone
Specific against Other
Appl. other
Host
Item no.
Amount 250 mg
Available
AC1-­IN-­38 Login AC1-IN-38
Type Chemicals
Clone
Specific against Other
Appl. other
Host
Item no.
Amount 1 g
Available
FGIN-­1-­27 Login FGIN-1-27
Type Chemicals
Clone
Specific against Other
Appl. FGIN-1-27 is an anxiolytic compound that acts as a selective agonist at the peripheral benzodiazepine receptor (TSPO).FGIN-1-27 inhibited Th17 cell differentiation, significantly downregulated the expression of RORγt target genes, notably Il17a, Il17f, Il23r, Ltb4r1, Ccr6.FGIN-1-27 protected mice against EAE, induced amino acid starvation response (AAR), FGIN-1-27 produced anti-anxiety and anti-panic effects in non-mammalian models.
Host
Item no.
Amount 100 mg
Available
FGIN-­1-­27 Login FGIN-1-27
Type Chemicals
Clone
Specific against Other
Appl. FGIN-1-27 is an anxiolytic compound that acts as a selective agonist at the peripheral benzodiazepine receptor (TSPO).FGIN-1-27 inhibited Th17 cell differentiation, significantly downregulated the expression of RORγt target genes, notably Il17a, Il17f, Il23r, Ltb4r1, Ccr6.FGIN-1-27 protected mice against EAE, induced amino acid starvation response (AAR), FGIN-1-27 produced anti-anxiety and anti-panic effects in non-mammalian models.
Host
Item no.
Amount 250 mg
Available
Bemcentinib（R428，BGB324) Login Bemcentinib（R428，BGB324)
Type Inhibitors
Clone
Specific against Other
Appl.
Host
Item no.
Amount 250 mg
Available
Bemcentinib（R428，BGB324) Login Bemcentinib（R428，BGB324)
Type Inhibitors
Clone
Specific against Other
Appl.
Host
Item no.
Amount 1 g
Available
Resminostat hydrochloride (4SC-­201) Login Resminostat hydrochloride (4SC-201)
Type Inhibitors
Clone
Specific against Other
Appl.
Host
Item no.
Amount 100 mg
Available
Resminostat hydrochloride (4SC-­201) Login Resminostat hydrochloride (4SC-201)
Type Inhibitors
Clone
Specific against Other
Appl.
Host
Item no.
Amount 250 mg
Available
Resminostat hydrochloride (4SC-­201) Login Resminostat hydrochloride (4SC-201)
Type Inhibitors
Clone
Specific against Other
Appl.
Host
Item no.
Amount 1 g
Available
LCS3 Login LCS3
Type Chemicals
Clone
Specific against Other
Appl. LCS3 inhibits glutathione disulfide reductase (GSR) and thioredoxin reductase 1 (TXNRD1) (IC50=3.3 µM and 3.8 µM, respectively) synergistically. LCS3 shows anti-tumor activity, and induces apoptosis. LCS3 can be used in lung adenocarcinoma (LUAD) research.
Host
Item no.
Amount 100 mg
Available
LCS3 Login LCS3
Type Chemicals
Clone
Specific against Other
Appl. LCS3 inhibits glutathione disulfide reductase (GSR) and thioredoxin reductase 1 (TXNRD1) (IC50=3.3 µM and 3.8 µM, respectively) synergistically. LCS3 shows anti-tumor activity, and induces apoptosis. LCS3 can be used in lung adenocarcinoma (LUAD) research.
Host
Item no.
Amount 250 mg
Available
LCS3 Login LCS3
Type Chemicals
Clone
Specific against Other
Appl. LCS3 inhibits glutathione disulfide reductase (GSR) and thioredoxin reductase 1 (TXNRD1) (IC50=3.3 µM and 3.8 µM, respectively) synergistically. LCS3 shows anti-tumor activity, and induces apoptosis. LCS3 can be used in lung adenocarcinoma (LUAD) research.
Host
Item no.
Amount 1 g
Available
LDCA Login LDCA
Type Chemicals
Clone
Specific against Other
Appl. LDCA is a dual-hit metabolic modulator and inhibits LDH-A enzyme activity to stimulate apoptosis in the malignant population. LDCA can be used for the research of oncogenic progression.
Host
Item no.
Amount 100 mg
Available
LDCA Login LDCA
Type Chemicals
Clone
Specific against Other
Appl. LDCA is a dual-hit metabolic modulator and inhibits LDH-A enzyme activity to stimulate apoptosis in the malignant population. LDCA can be used for the research of oncogenic progression.
Host
Item no.
Amount 250 mg
Available
LDCA Login LDCA
Type Chemicals
Clone
Specific against Other
Appl. LDCA is a dual-hit metabolic modulator and inhibits LDH-A enzyme activity to stimulate apoptosis in the malignant population. LDCA can be used for the research of oncogenic progression.
Host
Item no.
Amount 1 g
Available
GLN-­1062 Login GLN-1062
Type Chemicals
Clone
Specific against Other
Appl. GLN-1062 (Memogain) is an inactive pro-drug of galantamine, the latter being a plant alkaloid approved for the treatment of mild to moderate Alzheimer's disease.
Host
Item no.
Amount 100 mg
Available
GLN-­1062 Login GLN-1062
Type Chemicals
Clone
Specific against Other
Appl. GLN-1062 (Memogain) is an inactive pro-drug of galantamine, the latter being a plant alkaloid approved for the treatment of mild to moderate Alzheimer's disease.
Host
Item no.
Amount 250 mg
Available
GLN-­1062 Login GLN-1062
Type Chemicals
Clone
Specific against Other
Appl. GLN-1062 (Memogain) is an inactive pro-drug of galantamine, the latter being a plant alkaloid approved for the treatment of mild to moderate Alzheimer's disease.
Host
Item no.
Amount 1 g
Available
WAY-­296817 Login WAY-296817
Type Chemicals
Clone
Specific against Other
Appl. WAY-296817 is casein kinase 1 (CK1) inhibitor and can be used for research on the treatment or prevention.
Host
Item no.
Amount 100 mg
Available
WAY-­296817 Login WAY-296817
Type Chemicals
Clone
Specific against Other
Appl. WAY-296817 is casein kinase 1 (CK1) inhibitor and can be used for research on the treatment or prevention.
Host
Item no.
Amount 250 mg
Available
WAY-­296817 Login WAY-296817
Type Chemicals
Clone
Specific against Other
Appl. WAY-296817 is casein kinase 1 (CK1) inhibitor and can be used for research on the treatment or prevention.
Host
Item no.
Amount 1 g
Available

1437732 Item(s)

per page

Page:
  1. 26
  2. 27
  3. 28
  4. 29
  5. 30
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F +49 221 126 02 67

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