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1437728 Item(s)

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  2. 47
  3. 48
  4. 49
  5. 50
Name PDF Type Clone Specific against Appl. Host Item no. Amount ✓ Price
NSC 31152 Chemicals Other DCC-DC60209-100mg

DCChemicals 		100 mg Login
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NSC 31152 Chemicals Other DCC-DC60209-250mg

DCChemicals 		250 mg Login
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NSC 31152 Chemicals Other DCC-DC60209-1g

DCChemicals 		1 g Login
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NSC 31153 Chemicals Other DCC-DC60208-100mg

DCChemicals 		100 mg Login
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NSC 31153 Chemicals Other DCC-DC60208-250mg

DCChemicals 		250 mg Login
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NSC 31153 Chemicals Other DCC-DC60208-1g

DCChemicals 		1 g Login
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JNJ-­63576253 HCl Chemicals Other JNJ63576253, also known as TRC253, is a potent and orally active androgen receptor antagonist. TRC253 specifically binds to both wild-type and certain mutant forms of AR, thereby preventing androgen-induced receptor activation and facilitating the formation of inactive complexes that cannot translocate to the nucleus. DCC-DC60203-100mg

DCChemicals 		100 mg Login
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JNJ-­63576253 HCl Chemicals Other JNJ63576253, also known as TRC253, is a potent and orally active androgen receptor antagonist. TRC253 specifically binds to both wild-type and certain mutant forms of AR, thereby preventing androgen-induced receptor activation and facilitating the formation of inactive complexes that cannot translocate to the nucleus. DCC-DC60203-250mg

DCChemicals 		250 mg Login
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JNJ-­63576253 HCl Chemicals Other JNJ63576253, also known as TRC253, is a potent and orally active androgen receptor antagonist. TRC253 specifically binds to both wild-type and certain mutant forms of AR, thereby preventing androgen-induced receptor activation and facilitating the formation of inactive complexes that cannot translocate to the nucleus. DCC-DC60203-1g

DCChemicals 		1 g Login
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YUN35454 Chemicals Other YUN35454, also known as LMPTP INHIBITOR 1 is a selective inhibitor of low molecular weight protein tyrosine phosphatase (LMPTP), with an IC50 of 0.8 μM LMPTP-A. LMPTP is a key promoter of insulin resistance and that LMPTP inhibitors would be beneficial for treating type 2 diabetes. YUN35454 was first reported in Nature Chemical Biology (2017), 13(6), 624-632. DCC-DC60202-100mg

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YUN35454 Chemicals Other YUN35454, also known as LMPTP INHIBITOR 1 is a selective inhibitor of low molecular weight protein tyrosine phosphatase (LMPTP), with an IC50 of 0.8 μM LMPTP-A. LMPTP is a key promoter of insulin resistance and that LMPTP inhibitors would be beneficial for treating type 2 diabetes. YUN35454 was first reported in Nature Chemical Biology (2017), 13(6), 624-632. DCC-DC60202-250mg

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YUN35454 Chemicals Other YUN35454, also known as LMPTP INHIBITOR 1 is a selective inhibitor of low molecular weight protein tyrosine phosphatase (LMPTP), with an IC50 of 0.8 μM LMPTP-A. LMPTP is a key promoter of insulin resistance and that LMPTP inhibitors would be beneficial for treating type 2 diabetes. YUN35454 was first reported in Nature Chemical Biology (2017), 13(6), 624-632. DCC-DC60202-1g

DCChemicals 		1 g Login
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SR 18662 Chemicals Other FC, IV DCC-DC60201-100mg

DCChemicals 		100 mg Login
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SR 18662 Chemicals Other FC, IV DCC-DC60201-250mg

DCChemicals 		250 mg Login
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SR 18662 Chemicals Other FC, IV DCC-DC60201-1g

DCChemicals 		1 g Login
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K-­Ras G12C-­IN-­4 Chemicals Other DCC-DC60196-100mg

DCChemicals 		100 mg Login
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K-­Ras G12C-­IN-­4 Chemicals Other DCC-DC60196-250mg

DCChemicals 		250 mg Login
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K-­Ras G12C-­IN-­4 Chemicals Other DCC-DC60196-1g

DCChemicals 		1 g Login
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Bifluranol Chemicals Other Bifluranol (brand name Prostarex; former developmental code name BX-341) is a synthetic nonsteroidal estrogen of the stilbestrol group related to diethylstilbestrol that has been used as an antiandrogen in the United Kingdom in the treatment of benign pro, consequently suppressing the secretion of luteinizing hormone (and hence acting as an antigonadotropin) and thereby reducing gonadal androgen production and systemic androgen levels. DCC-DC60199-100mg

DCChemicals 		100 mg Login
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Bifluranol Chemicals Other consequently suppressing the secretion of luteinizing hormone (and hence acting as an antigonadotropin) and thereby reducing gonadal androgen production and systemic androgen levels., Bifluranol (brand name Prostarex; former developmental code name BX-341) is a synthetic nonsteroidal estrogen of the stilbestrol group related to diethylstilbestrol that has been used as an antiandrogen in the United Kingdom in the treatment of benign pro DCC-DC60199-250mg

DCChemicals 		250 mg Login
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Bifluranol Chemicals Other consequently suppressing the secretion of luteinizing hormone (and hence acting as an antigonadotropin) and thereby reducing gonadal androgen production and systemic androgen levels., Bifluranol (brand name Prostarex; former developmental code name BX-341) is a synthetic nonsteroidal estrogen of the stilbestrol group related to diethylstilbestrol that has been used as an antiandrogen in the United Kingdom in the treatment of benign pro DCC-DC60199-1g

DCChemicals 		1 g Login
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SEP-­363856 isomer Chemicals Other R isomer of SEP-363856. DCC-DC60200-100mg

DCChemicals 		100 mg Login
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SEP-­363856 isomer Chemicals Other R isomer of SEP-363856. DCC-DC60200-250mg

DCChemicals 		250 mg Login
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SEP-­363856 isomer Chemicals Other R isomer of SEP-363856. DCC-DC60200-1g

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GN44028 Chemicals Other GN44028 inhibits HIF-1α. GN44028 surpresses HIF-1α transcriptional activity without affecting both HIF-1α protein accumulation and HIF-1α/HIF-1β heterodimerization in nuclei under the hypoxic conditions, suggesting that GN44028 probably affectes the transcriptional pathway induced by the HIF-1α/HIF-1β heterodimer. DCC-DC60198-100mg

DCChemicals 		100 mg Login
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Name Price
NSC 31152 Login NSC 31152
Type Chemicals
Clone
Specific against Other
Appl.
Host
Item no.
Amount 100 mg
Available
NSC 31152 Login NSC 31152
Type Chemicals
Clone
Specific against Other
Appl.
Host
Item no.
Amount 250 mg
Available
NSC 31152 Login NSC 31152
Type Chemicals
Clone
Specific against Other
Appl.
Host
Item no.
Amount 1 g
Available
NSC 31153 Login NSC 31153
Type Chemicals
Clone
Specific against Other
Appl.
Host
Item no.
Amount 100 mg
Available
NSC 31153 Login NSC 31153
Type Chemicals
Clone
Specific against Other
Appl.
Host
Item no.
Amount 250 mg
Available
NSC 31153 Login NSC 31153
Type Chemicals
Clone
Specific against Other
Appl.
Host
Item no.
Amount 1 g
Available
JNJ-­63576253 HCl Login JNJ-63576253 HCl
Type Chemicals
Clone
Specific against Other
Appl. JNJ63576253, also known as TRC253, is a potent and orally active androgen receptor antagonist. TRC253 specifically binds to both wild-type and certain mutant forms of AR, thereby preventing androgen-induced receptor activation and facilitating the formation of inactive complexes that cannot translocate to the nucleus.
Host
Item no.
Amount 100 mg
Available
JNJ-­63576253 HCl Login JNJ-63576253 HCl
Type Chemicals
Clone
Specific against Other
Appl. JNJ63576253, also known as TRC253, is a potent and orally active androgen receptor antagonist. TRC253 specifically binds to both wild-type and certain mutant forms of AR, thereby preventing androgen-induced receptor activation and facilitating the formation of inactive complexes that cannot translocate to the nucleus.
Host
Item no.
Amount 250 mg
Available
JNJ-­63576253 HCl Login JNJ-63576253 HCl
Type Chemicals
Clone
Specific against Other
Appl. JNJ63576253, also known as TRC253, is a potent and orally active androgen receptor antagonist. TRC253 specifically binds to both wild-type and certain mutant forms of AR, thereby preventing androgen-induced receptor activation and facilitating the formation of inactive complexes that cannot translocate to the nucleus.
Host
Item no.
Amount 1 g
Available
YUN35454 Login YUN35454
Type Chemicals
Clone
Specific against Other
Appl. YUN35454, also known as LMPTP INHIBITOR 1 is a selective inhibitor of low molecular weight protein tyrosine phosphatase (LMPTP), with an IC50 of 0.8 μM LMPTP-A. LMPTP is a key promoter of insulin resistance and that LMPTP inhibitors would be beneficial for treating type 2 diabetes. YUN35454 was first reported in Nature Chemical Biology (2017), 13(6), 624-632.
Host
Item no.
Amount 100 mg
Available
YUN35454 Login YUN35454
Type Chemicals
Clone
Specific against Other
Appl. YUN35454, also known as LMPTP INHIBITOR 1 is a selective inhibitor of low molecular weight protein tyrosine phosphatase (LMPTP), with an IC50 of 0.8 μM LMPTP-A. LMPTP is a key promoter of insulin resistance and that LMPTP inhibitors would be beneficial for treating type 2 diabetes. YUN35454 was first reported in Nature Chemical Biology (2017), 13(6), 624-632.
Host
Item no.
Amount 250 mg
Available
YUN35454 Login YUN35454
Type Chemicals
Clone
Specific against Other
Appl. YUN35454, also known as LMPTP INHIBITOR 1 is a selective inhibitor of low molecular weight protein tyrosine phosphatase (LMPTP), with an IC50 of 0.8 μM LMPTP-A. LMPTP is a key promoter of insulin resistance and that LMPTP inhibitors would be beneficial for treating type 2 diabetes. YUN35454 was first reported in Nature Chemical Biology (2017), 13(6), 624-632.
Host
Item no.
Amount 1 g
Available
SR 18662 Login SR 18662
Type Chemicals
Clone
Specific against Other
Appl. FC, IV
Host
Item no.
Amount 100 mg
Available
SR 18662 Login SR 18662
Type Chemicals
Clone
Specific against Other
Appl. FC, IV
Host
Item no.
Amount 250 mg
Available
SR 18662 Login SR 18662
Type Chemicals
Clone
Specific against Other
Appl. FC, IV
Host
Item no.
Amount 1 g
Available
K-­Ras G12C-­IN-­4 Login K-Ras G12C-IN-4
Type Chemicals
Clone
Specific against Other
Appl.
Host
Item no.
Amount 100 mg
Available
K-­Ras G12C-­IN-­4 Login K-Ras G12C-IN-4
Type Chemicals
Clone
Specific against Other
Appl.
Host
Item no.
Amount 250 mg
Available
K-­Ras G12C-­IN-­4 Login K-Ras G12C-IN-4
Type Chemicals
Clone
Specific against Other
Appl.
Host
Item no.
Amount 1 g
Available
Bifluranol Login Bifluranol
Type Chemicals
Clone
Specific against Other
Appl. Bifluranol (brand name Prostarex; former developmental code name BX-341) is a synthetic nonsteroidal estrogen of the stilbestrol group related to diethylstilbestrol that has been used as an antiandrogen in the United Kingdom in the treatment of benign pro, consequently suppressing the secretion of luteinizing hormone (and hence acting as an antigonadotropin) and thereby reducing gonadal androgen production and systemic androgen levels.
Host
Item no.
Amount 100 mg
Available
Bifluranol Login Bifluranol
Type Chemicals
Clone
Specific against Other
Appl. consequently suppressing the secretion of luteinizing hormone (and hence acting as an antigonadotropin) and thereby reducing gonadal androgen production and systemic androgen levels., Bifluranol (brand name Prostarex; former developmental code name BX-341) is a synthetic nonsteroidal estrogen of the stilbestrol group related to diethylstilbestrol that has been used as an antiandrogen in the United Kingdom in the treatment of benign pro
Host
Item no.
Amount 250 mg
Available
Bifluranol Login Bifluranol
Type Chemicals
Clone
Specific against Other
Appl. consequently suppressing the secretion of luteinizing hormone (and hence acting as an antigonadotropin) and thereby reducing gonadal androgen production and systemic androgen levels., Bifluranol (brand name Prostarex; former developmental code name BX-341) is a synthetic nonsteroidal estrogen of the stilbestrol group related to diethylstilbestrol that has been used as an antiandrogen in the United Kingdom in the treatment of benign pro
Host
Item no.
Amount 1 g
Available
SEP-­363856 isomer Login SEP-363856 isomer
Type Chemicals
Clone
Specific against Other
Appl. R isomer of SEP-363856.
Host
Item no.
Amount 100 mg
Available
SEP-­363856 isomer Login SEP-363856 isomer
Type Chemicals
Clone
Specific against Other
Appl. R isomer of SEP-363856.
Host
Item no.
Amount 250 mg
Available
SEP-­363856 isomer Login SEP-363856 isomer
Type Chemicals
Clone
Specific against Other
Appl. R isomer of SEP-363856.
Host
Item no.
Amount 1 g
Available
GN44028 Login GN44028
Type Chemicals
Clone
Specific against Other
Appl. GN44028 inhibits HIF-1α. GN44028 surpresses HIF-1α transcriptional activity without affecting both HIF-1α protein accumulation and HIF-1α/HIF-1β heterodimerization in nuclei under the hypoxic conditions, suggesting that GN44028 probably affectes the transcriptional pathway induced by the HIF-1α/HIF-1β heterodimer.
Host
Item no.
Amount 100 mg
Available

1437728 Item(s)

per page

Page:
  1. 46
  2. 47
  3. 48
  4. 49
  5. 50
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