CSNpharm
CSNpharm
Tazarotene selectively binds to retinoic acid receptors RAR-β and RAR-γ, it is the first receptor-selective aromatic retinoid that has effective treatment for psoriasis, hemorrhoids.
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CSNpharm
Tazarotene selectively binds to retinoic acid receptors RAR-β and RAR-γ, it is the first receptor-selective aromatic retinoid that has effective treatment for psoriasis, hemorrhoids.
More Information
Supplier Page
CSNpharm
Tazarotene selectively binds to retinoic acid receptors RAR-β and RAR-γ, it is the first receptor-selective aromatic retinoid that has effective treatment for psoriasis, hemorrhoids.
More Information
Supplier Page
CSNpharm
Tazarotene selectively binds to retinoic acid receptors RAR-β and RAR-γ, it is the first receptor-selective aromatic retinoid that has effective treatment for psoriasis, hemorrhoids.
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CSNpharm
CSNpharm
TBB
50mg
| ≥99%
CSNpharm
TBB is a highly selective, ATP/GTP-competitive inhibitor of casein kinase-2 (CK2)with IC50s of 0.9 and 1.6 μM for rat liver and human recombinant CK2 respectively).
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TBB
10mg
| ≥99%
CSNpharm
TBB is a highly selective, ATP/GTP-competitive inhibitor of casein kinase-2 (CK2)with IC50s of 0.9 and 1.6 μM for rat liver and human recombinant CK2 respectively).
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CSNpharm
TBHBA can reacts with hydrogen peroxide and 4-aminophenazone to produce a quinone-imine dye with a greater molar absorptivity than that produced with phenol.
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TBHBA
250mg
| ≥98%
CSNpharm
TBHBA can reacts with hydrogen peroxide and 4-aminophenazone to produce a quinone-imine dye with a greater molar absorptivity than that produced with phenol.
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TBHQ
1g
| ≥99%
CSNpharm
CSNpharm
TC E3 5032 is a thalidomide derivate for conjugation reactions of PROTAC, which can hijack cereblon as the E3 ubiquitin ligase component.
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CSNpharm
TC E3 5032 is a thalidomide derivate for conjugation reactions of PROTAC, which can hijack cereblon as the E3 ubiquitin ligase component.
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CSNpharm
TC E3 5032 is a thalidomide derivate for conjugation reactions of PROTAC, which can hijack cereblon as the E3 ubiquitin ligase component.
More Information
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CSNpharm
TC E3 5032 is a thalidomide derivate for conjugation reactions of PROTAC, which can hijack cereblon as the E3 ubiquitin ligase component.
More Information
Supplier Page
CSNpharm
TC E3 5032 is a thalidomide derivate for conjugation reactions of PROTAC, which can hijack cereblon as the E3 ubiquitin ligase component.
More Information
Supplier Page
CSNpharm
CSNpharm
CSNpharm
CSNpharm
CSNpharm
TCID
1mg
| ≥98%
CSNpharm
TCID
5mg
| ≥98%
CSNpharm
CSNpharm
CSNpharm
CSNpharm
CSNpharm
CSNpharm
CSNpharm
CSNpharm
CSNpharm
CSNpharm
CSNpharm
CSNpharm
CSNpharm
CSNpharm
CSNpharm
CSNpharm
TDZD-8, the derivative of thiadiazolidinone, is a selective inhibitor of GSK-3. It inhibits GSK-3β with IC50 of 2 μM.
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CSNpharm
TDZD-8, the derivative of thiadiazolidinone, is a selective inhibitor of GSK-3. It inhibits GSK-3β with IC50 of 2 μM.
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CSNpharm
TDZD-8, the derivative of thiadiazolidinone, is a selective inhibitor of GSK-3. It inhibits GSK-3β with IC50 of 2 μM.
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CSNpharm
TDZD-8, the derivative of thiadiazolidinone, is a selective inhibitor of GSK-3. It inhibits GSK-3β with IC50 of 2 μM.
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TDZD-8
100mg
| ≥99%
CSNpharm
TDZD-8, the derivative of thiadiazolidinone, is a selective inhibitor of GSK-3. It inhibits GSK-3β with IC50 of 2 μM.
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CSNpharm
CSNpharm
CSNpharm
CSNpharm
CSNpharm
Tebipenem Pivoxil is a pivaloyloxymethyl ester prodrug of tebipenem with improved bioavailability, which works as a broad-spectrum antibiotic.
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CSNpharm
Tebipenem Pivoxil is a pivaloyloxymethyl ester prodrug of tebipenem with improved bioavailability, which works as a broad-spectrum antibiotic.
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CSNpharm
Tebipenem Pivoxil is a pivaloyloxymethyl ester prodrug of tebipenem with improved bioavailability, which works as a broad-spectrum antibiotic.
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