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1437732 Item(s)

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  2. 30
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  4. 32
  5. 33
Name PDF Type Clone Specific against Appl. Host Item no. Amount ✓ Price
API-­1(NSC 177223) Chemicals Other API-1 is a potent Akt inhibitor, which induces GSK3-dependent, β-TrCP- and FBXW7-mediated Mcl-1 degradation, resulting in induction of apoptosis . API-1 rapidly and potently reduced the levels of Mcl-1 primarily in API-1-senstive lung cancer cell lines. Ectopic expression of Mcl-1 protected cells from induction of apoptosis by API-1. DCC-DC60132-100mg

DCChemicals 		100 mg Login
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API-­1(NSC 177223) Chemicals Other API-1 is a potent Akt inhibitor, which induces GSK3-dependent, β-TrCP- and FBXW7-mediated Mcl-1 degradation, resulting in induction of apoptosis . API-1 rapidly and potently reduced the levels of Mcl-1 primarily in API-1-senstive lung cancer cell lines. Ectopic expression of Mcl-1 protected cells from induction of apoptosis by API-1. DCC-DC60132-250mg

DCChemicals 		250 mg Login
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API-­1(NSC 177223) Chemicals Other API-1 is a potent Akt inhibitor, which induces GSK3-dependent, β-TrCP- and FBXW7-mediated Mcl-1 degradation, resulting in induction of apoptosis . API-1 rapidly and potently reduced the levels of Mcl-1 primarily in API-1-senstive lung cancer cell lines. Ectopic expression of Mcl-1 protected cells from induction of apoptosis by API-1. DCC-DC60132-1g

DCChemicals 		1 g Login
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G244-­LM Chemicals Other G244-LM is a potent and specific inhibitor of tankyrase 1/2 that inhibits Wnt signaling. DCC-DC60131-100mg

DCChemicals 		100 mg Login
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G244-­LM Chemicals Other G244-LM is a potent and specific inhibitor of tankyrase 1/2 that inhibits Wnt signaling. DCC-DC60131-250mg

DCChemicals 		250 mg Login
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G244-­LM Chemicals Other G244-LM is a potent and specific inhibitor of tankyrase 1/2 that inhibits Wnt signaling. DCC-DC60131-1g

DCChemicals 		1 g Login
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KB-­0742 HCl Chemicals Other KB-0742 is an orally bioavailable, selective CDK9 inhibitor with potent anti-tumor activity in CRPC models. DCC-DC60126-100mg

DCChemicals 		100 mg Login
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KB-­0742 HCl Chemicals Other KB-0742 is an orally bioavailable, selective CDK9 inhibitor with potent anti-tumor activity in CRPC models. DCC-DC60126-250mg

DCChemicals 		250 mg Login
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KB-­0742 HCl Chemicals Other KB-0742 is an orally bioavailable, selective CDK9 inhibitor with potent anti-tumor activity in CRPC models. DCC-DC60126-1g

DCChemicals 		1 g Login
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NVP-­BHG712 isomer Chemicals Other other DCC-DC60121-100mg

DCChemicals 		100 mg Login
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NVP-­BHG712 isomer Chemicals Other other DCC-DC60121-250mg

DCChemicals 		250 mg Login
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NVP-­BHG712 isomer Chemicals Other other DCC-DC60121-1g

DCChemicals 		1 g Login
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YQ128 Chemicals Other IV DCC-DC60119-100mg

DCChemicals 		100 mg Login
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YQ128 Chemicals Other IV DCC-DC60119-250mg

DCChemicals 		250 mg Login
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YQ128 Chemicals Other IV DCC-DC60119-1g

DCChemicals 		1 g Login
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Fezolinetant HCl Chemicals Other Fezolinetant, also known as ESN-364, is Neurokinin-3 (NK-3) receptor antagonist which has been optimized for use in women’s health, and is being developed for sex-hormone related disorders such as endometriosis, polycystic ovarian syndrome and uterine fibroids. DCC-DC60118-100mg

DCChemicals 		100 mg Login
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Fezolinetant HCl Chemicals Other Fezolinetant, also known as ESN-364, is Neurokinin-3 (NK-3) receptor antagonist which has been optimized for use in women’s health, and is being developed for sex-hormone related disorders such as endometriosis, polycystic ovarian syndrome and uterine fibroids. DCC-DC60118-250mg

DCChemicals 		250 mg Login
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Fezolinetant HCl Chemicals Other Fezolinetant, also known as ESN-364, is Neurokinin-3 (NK-3) receptor antagonist which has been optimized for use in women’s health, and is being developed for sex-hormone related disorders such as endometriosis, polycystic ovarian syndrome and uterine fibroids. DCC-DC60118-1g

DCChemicals 		1 g Login
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Enfuvirtide Acetate Chemicals Other Enfuvirtide acetate salt is a linear synthetic peptide made of 36 amino acids. It has an acetylated N-terminus and a carboxamide C-terminus. DCC-DC60115-100mg

DCChemicals 		100 mg Login
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Enfuvirtide Acetate Chemicals Other Enfuvirtide acetate salt is a linear synthetic peptide made of 36 amino acids. It has an acetylated N-terminus and a carboxamide C-terminus. DCC-DC60115-250mg

DCChemicals 		250 mg Login
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Enfuvirtide Acetate Chemicals Other Enfuvirtide acetate salt is a linear synthetic peptide made of 36 amino acids. It has an acetylated N-terminus and a carboxamide C-terminus. DCC-DC60115-1g

DCChemicals 		1 g Login
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Ginkgolic acid C17:1 Chemicals Other Ginkgolic acid C17:1 (GAC 17:1) 通过废除上游的 JAK2 和 Src 来抑制 STAT3 的组成性激活。Ginkgolic acid C17:1 可以诱导 PTEN 和 SHP-1 的大量表达。Ginkgolic acid C17:1 诱导肿瘤细胞凋亡。 DCC-DC60112-100mg

DCChemicals 		100 mg Login
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Ginkgolic acid C17:1 Chemicals Other Ginkgolic acid C17:1 (GAC 17:1) 通过废除上游的 JAK2 和 Src 来抑制 STAT3 的组成性激活。Ginkgolic acid C17:1 可以诱导 PTEN 和 SHP-1 的大量表达。Ginkgolic acid C17:1 诱导肿瘤细胞凋亡。 DCC-DC60112-250mg

DCChemicals 		250 mg Login
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Ginkgolic acid C17:1 Chemicals Other Ginkgolic acid C17:1 (GAC 17:1) 通过废除上游的 JAK2 和 Src 来抑制 STAT3 的组成性激活。Ginkgolic acid C17:1 可以诱导 PTEN 和 SHP-1 的大量表达。Ginkgolic acid C17:1 诱导肿瘤细胞凋亡。 DCC-DC60112-1g

DCChemicals 		1 g Login
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CAY10781 Chemicals Other DCC-DC60110-100mg

DCChemicals 		100 mg Login
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Name Price
API-­1(NSC 177223) Login API-1(NSC 177223)
Type Chemicals
Clone
Specific against Other
Appl. API-1 is a potent Akt inhibitor, which induces GSK3-dependent, β-TrCP- and FBXW7-mediated Mcl-1 degradation, resulting in induction of apoptosis . API-1 rapidly and potently reduced the levels of Mcl-1 primarily in API-1-senstive lung cancer cell lines. Ectopic expression of Mcl-1 protected cells from induction of apoptosis by API-1.
Host
Item no.
Amount 100 mg
Available
API-­1(NSC 177223) Login API-1(NSC 177223)
Type Chemicals
Clone
Specific against Other
Appl. API-1 is a potent Akt inhibitor, which induces GSK3-dependent, β-TrCP- and FBXW7-mediated Mcl-1 degradation, resulting in induction of apoptosis . API-1 rapidly and potently reduced the levels of Mcl-1 primarily in API-1-senstive lung cancer cell lines. Ectopic expression of Mcl-1 protected cells from induction of apoptosis by API-1.
Host
Item no.
Amount 250 mg
Available
API-­1(NSC 177223) Login API-1(NSC 177223)
Type Chemicals
Clone
Specific against Other
Appl. API-1 is a potent Akt inhibitor, which induces GSK3-dependent, β-TrCP- and FBXW7-mediated Mcl-1 degradation, resulting in induction of apoptosis . API-1 rapidly and potently reduced the levels of Mcl-1 primarily in API-1-senstive lung cancer cell lines. Ectopic expression of Mcl-1 protected cells from induction of apoptosis by API-1.
Host
Item no.
Amount 1 g
Available
G244-­LM Login G244-LM
Type Chemicals
Clone
Specific against Other
Appl. G244-LM is a potent and specific inhibitor of tankyrase 1/2 that inhibits Wnt signaling.
Host
Item no.
Amount 100 mg
Available
G244-­LM Login G244-LM
Type Chemicals
Clone
Specific against Other
Appl. G244-LM is a potent and specific inhibitor of tankyrase 1/2 that inhibits Wnt signaling.
Host
Item no.
Amount 250 mg
Available
G244-­LM Login G244-LM
Type Chemicals
Clone
Specific against Other
Appl. G244-LM is a potent and specific inhibitor of tankyrase 1/2 that inhibits Wnt signaling.
Host
Item no.
Amount 1 g
Available
KB-­0742 HCl Login KB-0742 HCl
Type Chemicals
Clone
Specific against Other
Appl. KB-0742 is an orally bioavailable, selective CDK9 inhibitor with potent anti-tumor activity in CRPC models.
Host
Item no.
Amount 100 mg
Available
KB-­0742 HCl Login KB-0742 HCl
Type Chemicals
Clone
Specific against Other
Appl. KB-0742 is an orally bioavailable, selective CDK9 inhibitor with potent anti-tumor activity in CRPC models.
Host
Item no.
Amount 250 mg
Available
KB-­0742 HCl Login KB-0742 HCl
Type Chemicals
Clone
Specific against Other
Appl. KB-0742 is an orally bioavailable, selective CDK9 inhibitor with potent anti-tumor activity in CRPC models.
Host
Item no.
Amount 1 g
Available
NVP-­BHG712 isomer Login NVP-BHG712 isomer
Type Chemicals
Clone
Specific against Other
Appl. other
Host
Item no.
Amount 100 mg
Available
NVP-­BHG712 isomer Login NVP-BHG712 isomer
Type Chemicals
Clone
Specific against Other
Appl. other
Host
Item no.
Amount 250 mg
Available
NVP-­BHG712 isomer Login NVP-BHG712 isomer
Type Chemicals
Clone
Specific against Other
Appl. other
Host
Item no.
Amount 1 g
Available
YQ128 Login YQ128
Type Chemicals
Clone
Specific against Other
Appl. IV
Host
Item no.
Amount 100 mg
Available
YQ128 Login YQ128
Type Chemicals
Clone
Specific against Other
Appl. IV
Host
Item no.
Amount 250 mg
Available
YQ128 Login YQ128
Type Chemicals
Clone
Specific against Other
Appl. IV
Host
Item no.
Amount 1 g
Available
Fezolinetant HCl Login Fezolinetant HCl
Type Chemicals
Clone
Specific against Other
Appl. Fezolinetant, also known as ESN-364, is Neurokinin-3 (NK-3) receptor antagonist which has been optimized for use in women’s health, and is being developed for sex-hormone related disorders such as endometriosis, polycystic ovarian syndrome and uterine fibroids.
Host
Item no.
Amount 100 mg
Available
Fezolinetant HCl Login Fezolinetant HCl
Type Chemicals
Clone
Specific against Other
Appl. Fezolinetant, also known as ESN-364, is Neurokinin-3 (NK-3) receptor antagonist which has been optimized for use in women’s health, and is being developed for sex-hormone related disorders such as endometriosis, polycystic ovarian syndrome and uterine fibroids.
Host
Item no.
Amount 250 mg
Available
Fezolinetant HCl Login Fezolinetant HCl
Type Chemicals
Clone
Specific against Other
Appl. Fezolinetant, also known as ESN-364, is Neurokinin-3 (NK-3) receptor antagonist which has been optimized for use in women’s health, and is being developed for sex-hormone related disorders such as endometriosis, polycystic ovarian syndrome and uterine fibroids.
Host
Item no.
Amount 1 g
Available
Enfuvirtide Acetate Login Enfuvirtide Acetate
Type Chemicals
Clone
Specific against Other
Appl. Enfuvirtide acetate salt is a linear synthetic peptide made of 36 amino acids. It has an acetylated N-terminus and a carboxamide C-terminus.
Host
Item no.
Amount 100 mg
Available
Enfuvirtide Acetate Login Enfuvirtide Acetate
Type Chemicals
Clone
Specific against Other
Appl. Enfuvirtide acetate salt is a linear synthetic peptide made of 36 amino acids. It has an acetylated N-terminus and a carboxamide C-terminus.
Host
Item no.
Amount 250 mg
Available
Enfuvirtide Acetate Login Enfuvirtide Acetate
Type Chemicals
Clone
Specific against Other
Appl. Enfuvirtide acetate salt is a linear synthetic peptide made of 36 amino acids. It has an acetylated N-terminus and a carboxamide C-terminus.
Host
Item no.
Amount 1 g
Available
Ginkgolic acid C17:1 Login Ginkgolic acid C17:1
Type Chemicals
Clone
Specific against Other
Appl. Ginkgolic acid C17:1 (GAC 17:1) 通过废除上游的 JAK2 和 Src 来抑制 STAT3 的组成性激活。Ginkgolic acid C17:1 可以诱导 PTEN 和 SHP-1 的大量表达。Ginkgolic acid C17:1 诱导肿瘤细胞凋亡。
Host
Item no.
Amount 100 mg
Available
Ginkgolic acid C17:1 Login Ginkgolic acid C17:1
Type Chemicals
Clone
Specific against Other
Appl. Ginkgolic acid C17:1 (GAC 17:1) 通过废除上游的 JAK2 和 Src 来抑制 STAT3 的组成性激活。Ginkgolic acid C17:1 可以诱导 PTEN 和 SHP-1 的大量表达。Ginkgolic acid C17:1 诱导肿瘤细胞凋亡。
Host
Item no.
Amount 250 mg
Available
Ginkgolic acid C17:1 Login Ginkgolic acid C17:1
Type Chemicals
Clone
Specific against Other
Appl. Ginkgolic acid C17:1 (GAC 17:1) 通过废除上游的 JAK2 和 Src 来抑制 STAT3 的组成性激活。Ginkgolic acid C17:1 可以诱导 PTEN 和 SHP-1 的大量表达。Ginkgolic acid C17:1 诱导肿瘤细胞凋亡。
Host
Item no.
Amount 1 g
Available
CAY10781 Login CAY10781
Type Chemicals
Clone
Specific against Other
Appl.
Host
Item no.
Amount 100 mg
Available

1437732 Item(s)

per page

Page:
  1. 29
  2. 30
  3. 31
  4. 32
  5. 33
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