34 Results for "

STS

" in MedChemExpress (MCE) Product Catalog:
Products (34)

34 Results for "STS" in MCE Product Catalog:

227
227 Publications Verification
Cat. No.: HY-15141
CAS No.: 62996-74-1
Purity:  99.52%
Synonyms: Antibiotic AM-2282; STS; AM-2282
Staurosporine is a potent, ATP-competitive and non-selective inhibitor of protein kinases with IC50s of 6 nM, 15 nM, 2 nM, and 3 nM for PKC, PKA, c-Fgr, and Phosphorylase kinase respectively. Staurosporine also inhibits TAOK2 with an IC50 of 3 μM. Staurosporine is an apoptosis inducer .
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3
3 Cited Publications
Cat. No.: HY-B0084
CAS No.: 65928-58-7
Synonyms: STS 557
Target:  

Progesterone Receptor

Research Areas:  

Endocrinology

Dienogest (STS-557) is an orally active and selective progesterone receptor agonist that effectively reduces the gene expression of COX-2, mPGES-1 and aromatase. Dienogest also inhibits the mRNA and protein expression of PGE2 synthase and the activation of NF-κB. Dienogest can be used in studies of endometriosis, menopause and menorrhagia .
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1
1 Cited Publications
Cat. No.: HY-112944A
Synonyms: CMP-NeuNAz sodium; CMP-Neu5Az sodium
Target:  

Sialyltransferase

Research Areas:  

Infection

CMP-SiaNAz (CMP-NeuNAz) sodium is a sialic acid nucleotide sugar derivative. CMP-SiaNAz sodium is integrated into the glycosidic chain through the action of STs in the Golgi apparatus, forming SiaNAz substances. CMP-SiaNAz sodium can serve as a substrate for bacterial-derived sialic acid transferases and is used for chemical enzymatic labeling and imaging of cell surface glycosides .
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1
1 Cited Publications
Cat. No.: HY-P74484
Purity:  ≥ 95%, as determined by Bis-Tris PAGE.
Synonyms: Ubiquitin-associated and SH3 domain-containing protein B; STS-1; TULA-2; UBASH3B
Species:  
Source:  
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1
1 Cited Publications
Cat. No.: HY-P76687
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: Ubiquitin-associated and SH3 domain-containing protein A; CLIP4; STS-2; TULA-1
Species:  
Source:  
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Cat. No.: HY-15141G
CAS No.: 62996-74-1
Synonyms: Antibiotic AM-2282 (GMP); STS (GMP); AM-2282 (GMP)
Staurosporine (AM-2282) (GMP) is Staurosporine (HY-15141) produced by using GMP guidelines. GMP small molecules works appropriately as an auxiliary reagent for cell therapy manufacture. Staurosporine is a potent, ATP-competitive and non-selective inhibitor of protein kinases .
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Cat. No.: HY-W062700
CAS No.: 1609980-39-3
Research Areas:  

Neurological Disease

STS-E412 is a selective activator of tissue-protective EPO receptor (including EPOR and CD131). STS-E412 can be used for research of neurodegenerative diseases and organ protection .
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Cat. No.: HY-14585
CAS No.: 148672-09-7
Purity:  99.99%
Synonyms: Estrone 3-O-sulfamate
Target:  

Steroid Sulfatase

Research Areas:  

Cancer

Estrone O-sulfamate (Estrone 3-O-sulfamate) is a potent steroid sulfatase (STS) inhibitor. Estrone O-sulfamate has inhibitory activity for STS in a placental microsomes (P.M.) preparation and in MCF-7 cells with IC50 values of 18 nM and 0.83 nM, respectively. Estrone O-sulfamate can be used for the research of cancer .
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Cat. No.: HY-15141R
CAS No.: 62996-74-1
Synonyms: Antibiotic AM-2282 (Standard); STS (Standard); AM-2282 (Standard)
Staurosporine (Standard) is the analytical standard of Staurosporine. This product is intended for research and analytical applications. Staurosporine is a potent, ATP-competitive and non-selective inhibitor of protein kinases with IC50s of 6 nM, 15 nM, 2 nM, and 3 nM for PKC, PKA, c-Fgr, and Phosphorylase kinase respectively. Staurosporine also inhibits TAOK2 with an IC50 of 3 μM. Staurosporine is an apoptosis inducer[1][2][3][4][5].
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Cat. No.: HY-B0084R
CAS No.: 65928-58-7
Synonyms: STS 557 (Standard)
Research Areas:  

Endocrinology

Dienogest (Standard) is the analytical standard of Dienogest. This product is intended for research and analytical applications. Dienogest (STS-557) is an orally active and selective progesterone receptor agonist that effectively reduces the gene expression of COX-2, mPGES-1 and aromatase. Dienogest also inhibits the mRNA and protein expression of PGE2 synthase and the activation of NF-κB. Dienogest can be used in studies of endometriosis, menopause and menorrhagia .
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Cat. No.: HY-B0084S2
Synonyms: STS 557-d6
Dienogest-d6 is deuterium labeled Dienogest (HY-B0084). Dienogest is an orally active progesterone receptor agonist that can be used in the study of endometriosis .
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Cat. No.: HY-123868
CAS No.: 284045-56-3
Target:  

Steroid Sulfatase

Research Areas:  

Cancer

KW-2581 is a steroidal selective steroid sulfatase (STS) inhibitor with an IC50 of 4 nM. KW-2581 inhibits STS activity of ZR-75-1 cells with an IC50 of 13 nM. KW-2581 inhibits the E1S-stimulated growth of ZR-75-1 cells with an IC50 of 0.18 nM. KW-2581 inhibits sulfated-estrogen dependent growth of breast cancer cells both in vitro and in vivo. KW-2581 induced regression in E1S-induced tumor growth. KW-2581 can be studied in research on hormone receptors-positive breast cancer .
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Cat. No.: HY-175869
CAS No.: 3096878-87-1
Target:  

Ferroptosis

Ferroptosis-IN-22 is a selective ferroptosis inhibitor by targeting NCOA4 and disrupting its interaction with ferritin with an EC50 of 520 nM and a Kd of 0.78 μM. Ferroptosis-IN-22 has a strong inhibitory activity against ferroptosis induced by multiple ferroptosis inducers (RSL3 (HY-100218A), Erastin (HY-15763), ML210 (HY-100003), FIN56 (HY-103087)), but does not inhibit necrosis induced by H2O2 or apoptosis induced by STS (HY-15141). Ferroptosis-IN-22 effectively ameliorates Concanavalin A (HY-P2149)-induced acute liver injury. Ferroptosis-IN-22 can be used for the study of ferroptosis-related diseases .
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Cat. No.: HY-156511
CAS No.: 1464150-99-9
Target:  

MNK

Research Areas:  

Cancer

ETC-168 is a selective and oral active MNK inhibitor with the IC50 values of 23 and 43 nM against MNK1 and MNK2, respectively. ETC-168 shows antiproliferative efficacy in vivo and in vitro .
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Cat. No.: HY-155235
Target:  

Steroid Sulfatase

Research Areas:  

Cancer

Steroid sulfatase-IN-7 is an irreversible steroid sulfatase (STS) inhibitor with an IC50 value of 0.05 nM against human placental STS and can be used in cancer research .
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Cat. No.: HY-RS13969
Research Areas:  

Others

STS Human Pre-designed siRNA Set A contains three designed siRNAs for STS gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-RS22956
Research Areas:  

Others

Sts Rat Pre-designed siRNA Set A contains three designed siRNAs for Sts gene (Rat), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-156902
CAS No.: 345222-92-6
Target:  

Steroid Sulfatase

Research Areas:  

Others

Steroid sulfatase-IN-8 (7) is a STS inhibitor with PM IC50 value of 1 nM, JEG-3 IC50 of 0.025 nM, respecively .
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Cat. No.: HY-155234
Target:  

Steroid Sulfatase

Research Areas:  

Cancer

Steroid sulfatase-IN-6 (Compound 10c) is an irreversible inhibitor of steroid sulfatase (STS). Steroid sulfatase-IN-6 has an Ki value of 0.4 nM for human placenta STS. Steroid sulfatase-IN-6 can be used for tumor diseases research .
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Cat. No.: HY-123773
CAS No.: 943344-76-1
Synonyms: NSC 732011; HLX-801
Research Areas:  

Cancer

SR-16157 (NSC 732011; HLX-801) is a dual-action steroid sulfatase (STS) inhibitor (IC50 = 0.1 uM) and selective ERα modulator. SR-16157 exhibits STS inhibitory and anti-estrogenic effects in breast cancer cells. SR-16157 may be used in breast cancer research .
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