40 Results for "

SRC-1

" in MedChemExpress (MCE) Product Catalog:
Products (40)

40 Results for "SRC-1" in MCE Product Catalog:

11
11 Publications Verification
Cat. No.: HY-114421
CAS No.: 2064175-41-1
Purity:  99.89%
Synonyms: dTAG-13
Research Areas:  

Cancer

FKBP12 PROTAC dTAG-13 (dTAG-13) is a FKBP12 F36V PROTAC degrader and a PXR partial agonist. FKBP12 PROTAC dTAG-13 induces ubiquitination and proteasomal degradation of proteins tagged with FKBP12 F36V, without degrading wild-type FKBP12 or un-fused PXR. It weakly promotes the recruitment of SRC-1, strongly inhibits the interaction between NCoR and PXR, and upregulates the expression of CYP3A4 and other drug metabolism-related genes. FKBP12 PROTAC dTAG-13 is applicable to research related to breast cancer and leukemia [1] .
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7
7 Cited Publications
Cat. No.: HY-112096
CAS No.: 1914078-41-3
Purity:  99.17%
Synonyms: NXP900
Target:  

Src

Research Areas:  

Cancer

eCF506 (NXP900) is a highly potent and orally active YES1/SRC kinase inhibitor with an IC50 of 0.47 nM. eCF506 locks its target into its native “closed” conformation, thereby inhibiting both kinase activity and complex formation with protein partners. eCF506 can be used for the study of esophageal squamous cancer and breast cancer [1].
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2
2 Cited Publications
Cat. No.: HY-123402
CAS No.: 264206-85-1
Purity:  99.19%
Target:  

LXR

Research Areas:  

Metabolic Disease

GSK3987 is a pan LXRα/β agonist with EC50s of 50 nM, 40 nM for LXRα-SRC1 and LXRβ-SRC1, respectively. GSK3987 increases the expression of ABCA1 and SREBP-1c. GSK3987 induces cellular cholesterol efflux and triglyceride accumulation [1].
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1
1 Cited Publications
Cat. No.: HY-15606
CAS No.: 304853-42-7
Purity:  99.87%
Synonyms: NSP-989
Target:  

Progesterone Receptor

Research Areas:  

Endocrinology

Tanaproget is an orally effective, selective nonsteroidal progesterone receptor (PR) agonist targeting human PR with an IC50 of 1.7 nM. Tanaproget promotes the interaction between PR receptors and coactivators (such as SRC-1), thereby inhibiting the secretion of matrix metalloproteinases (MMP-3/MMP-7) and reducing endometrial tissue invasion and angiogenesis. Tanaproget can be used for contraception and endometriosis inhibition research [1] .
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1
1 Cited Publications
Cat. No.: HY-153833
CAS No.: 2904682-19-3
Purity:  99.77%
Synonyms: KVA-E-23A
Target:  

Gap Junction Protein

Research Areas:  

Cancer

PDS-0330 is a specific and potent Claudin-1 inhibitor. PDS-0330 interferes with claudin-1/Src association and inhibits colorectal cancer (CRC) progression and metastasis [1].
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1
1 Cited Publications
Cat. No.: HY-P701321
Purity:  ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: SRC; Tyrosine Kinase Pp60c-SRC; Prev. SRC1; P60-SRC; C-SRC; Protooncogene SRC, Rous Sarcoma; ASV; Tyrosine-Protein Kinase SRC-1; V-SRC Avian Sarcoma (Schmidt-Ruppin A-2) Viral Oncogene Homolog; Pp60c-SRC; Proto-Oncogene Tyrosine-Protein Kinase SRC; THC6;
Species:  
Source:  
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Cat. No.: HY-P5464
CAS No.: 227929-80-8
Target:  

Estrogen Receptor/ERR

Research Areas:  

Others

SRC-1 NR box peptide is a biological active peptide (This peptide is a 14-amino acid fragment from the steroid receptor cofactor SRC-1 NR II). SRC-1 NR box peptide can be used to study the regulatory mechanisms of estrogen receptor ligands [1].
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Cat. No.: HY-P5464A
Target:  

Estrogen Receptor/ERR

Research Areas:  

Endocrinology

SRC-1 NR box peptide acetate is a biological active peptide (This peptide is a 14-amino acid fragment from the steroid receptor cofactor SRC-1 NR II). SRC-1 NR box peptide acetate can be used to study the regulatory mechanisms of estrogen receptor ligands [1].
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Cat. No.: HY-117819
CAS No.: 1421837-45-7
Purity:  99.81%
Target:  

ROR

Research Areas:  

Inflammation/Immunology

TMP920 is a highly potent and selective RORγt antagonist. TMP920 inhibits RORγt binding to the SRC1 peptide with an IC50 of 0.03 μM [1].
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Cat. No.: HY-156914
CAS No.: 852367-46-5
Purity:  99.86%
Target:  

IGF-1R Src

Research Areas:  

Cancer

IGF-1R/SRC-IN-1 (Compound 3b) is an inhibitor for IGF-1R (IC50 is 63 μM) and SRC .
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Cat. No.: HY-P5458
CAS No.: 394658-24-3
Research Areas:  

Others

SRC-1 (686-700) is a biological active peptide. (This peptide is amino acids 686 to 700 fragment containing the second LXXLL motif, derived from NR box II of steroid receptor coactivator (SRC1). Coactivator proteins interact with nuclear receptors in a ligand-dependent manner and augment transcription.)
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Cat. No.: HY-RS13749
Research Areas:  

Others

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

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Cat. No.: HY-RS09089
Research Areas:  

Others

NCOA1 Human Pre-designed siRNA Set A contains three designed siRNAs for NCOA1 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-P3773
CAS No.: 168781-78-0
Target:  

Src

Research Areas:  

Cancer

p60c-src substrate II is an efficient pentapeptide substrate for the tyrosine kinase pp60c-src .
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Cat. No.: HY-175264
CAS No.: 2530027-77-9
MI891 is a highly selective PXR antagonist (IC50 = 3.76 μM, Kd = 1.7 μM) and inverse agonist (IC50 = 6.1 μM). MI891 selectively disrupts the interaction between PXR and its coactivator SRC1. MI891 effectively inhibits Rifampicin (HY-B0272)-induced PXR activation. MI891 is useful for the study of metabolic diseases and other diseases [1].
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Cat. No.: HY-112096S
Synonyms: NXP900-d5
eCF506-d5 (NXP900-d5) is deuterated labeled eCF506 (HY-112096). eCF506 is a highly potent and orally active YES1/SRC kinase inhibitor with an IC50 of 0.47 nM. eCF506 locks its target into its native “closed” conformation, thereby inhibiting both kinase activity and complex formation with protein partners. eCF506 can be used for the study of esophageal squamous cancer and breast cancer [1] .
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Cat. No.: HY-P5559
CAS No.: 2582803-80-1
Target:  

PROTACs

Research Areas:  

Cancer

ND1-YL2 is a PROTAC that selectively degrades SRC-1 via the N-degron pathway. ND1-YL2 significantly inhibits cancer invasion and migration in vitro and in vivo. ND1-YL2 can be used in cancer research [1].
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Cat. No.: HY-139562
CAS No.: 2314378-09-9
Target:  

FXR

Research Areas:  

Metabolic Disease

BMS-986318 is a potent nonbile acid FXR agonist with EC50s of 53 and 350 nM in the FXR Gal4 and SRC-1 recruitment assays, respectively. BMS-986318 has a suitable ADME profile, and demonstrates efficacy in the mouse bile duct ligation model of liver cholestasis and fibrosis.BMS-986318 can be used for the research of nonalcoholic steatohepatitis [1].
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Cat. No.: HY-P81990
Synonyms: bHLHe74; mNRC 1; NCoA 1; RIP160; SRC 1

Host:  

Rabbit

Application:  

WB, IHC-P, IP

Reactivity:  

Human

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Cat. No.: HY-P81990A
Synonyms: bHLHe74; mNRC 1; NCoA 1; RIP160; SRC 1

Host:  

Rabbit

Application:  

WB, IHC-P, IP

Reactivity:  

Human

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