20 Results for "

3-AP

" in MedChemExpress (MCE) Product Catalog:
Products (20)

20 Results for "3-AP" in MCE Product Catalog:

11
11 Publications Verification
Cat. No.: HY-10082
CAS No.: 143621-35-6
Purity:  99.78%
Synonyms: 3-AP; PAN-811; OCX191
Target:  

DNA/RNA Synthesis

Research Areas:  

Cancer

Triapine (3-AP; PAN-811) is a potent inhibitor of the M2 subunit of ribonucleotide reductase (RR), and is a potent radiosensitizer.
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1 Cited Publications
Cat. No.: HY-100786
CAS No.: 5652-28-8
Purity:  ≥98.0%
DL-AP3 is a competitive mGluR1 and mGluR5 antagonist. DL-AP3 is also an inhibitor of phosphoserine phosphatase. DL-AP3 has neuroprotective effect [3].
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Cat. No.: HY-108546
CAS No.: 23052-80-4
Synonyms: 3-Phosphono-L-alanine
Target:  

mGluR

Research Areas:  

Neurological Disease

L-AP3, metabotropic glutamate receptor (mGluR) antagonist, inhibits D-phosphoserine and L-phosphoserine with IC50s of 368 μM and 2087 μM, respectively .
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Cat. No.: HY-10082B
CAS No.: 216240-62-9
Synonyms: 3-AP hydrochloride; PAN-811 hydrochloride; OCX191 hydrochloride
Target:  

DNA/RNA Synthesis

Research Areas:  

Cancer

Triapine (hydrochloride) is the hydrochloride form of Triapine (HY-10082). Triapine (3-AP; PAN-811) is a potent inhibitor of the M2 subunit of ribonucleotide reductase (RR), and is a potent radiosensitizer .
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Cat. No.: HY-10082A
CAS No.: 200933-27-3
Synonyms: (E)-PAN-811; (E)-NSC# 663249; (E)-OCX191
Target:  

DNA/RNA Synthesis

Research Areas:  

Cancer

(E)-3-AP is the E configuration of 3-AP. 3-AP is a potent ribonucleotide reductase inhibitor. 3-AP shows anti-proliferative activity. 3-AP shows anticancer activity in L1210 leukemia model. 3-AP inhibits RR activity and DNA synthesis .
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Cat. No.: HY-10082R
CAS No.: 143621-35-6
Synonyms: 3-AP (Standard); PAN-811 (Standard); OCX191 (Standard)
Research Areas:  

Cancer

Triapine (Standard) is the analytical standard of Triapine (HY-10082). This product is intended for research and analytical applications. Triapine (3-AP; PAN-811) is a potent inhibitor of the M2 subunit of ribonucleotide reductase (RR), and is a potent radiosensitizer.
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Cat. No.: HY-138844
CAS No.: 1184391-57-8
3-AP-Me is a dimethyl derivative of the nucleotide reductase inhibitor 3-AP (SML0568). 3-AP-Me can activate the endoplasmic reticulum (ER) stress pathway by promoting the phosphorylation of eIF2α and increasing the gene expression of transcription factors ATF4 and ATF6, leading to cell apoptosis. Additionally, 3-AP-Me can activate the stress kinases c-Jun N-terminal kinase (JNK) and p38 mitogen-activated protein kinases. 3-AP-Me also leads to the upregulation of the spliced mRNA variant XBP1, can be used in cancer research .
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Cat. No.: HY-10082S1
Synonyms: 3-AP-d3; PAN-811-d3; OCX191-d3
Triapine-d3 (3-AP-d3) is deuterium labeled Triapine. Triapine (3-AP; PAN-811) is a potent inhibitor of the M2 subunit of ribonucleotide reductase (RR), and is a potent radiosensitizer.
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Cat. No.: HY-P2434
CAS No.: 846569-60-6
AP102 is a dual SSTR2/SSTR5-specific somatostatin analog (SSA). AP102 is a disulfide-bridged octapeptide SSA containing synthetic iodinated amino acids. AP102 binds with subnanomolar affinity to SSTR2 and SSTR5 (IC50: 0.63 and 0.65 nM, respectively). AP102 does not bind to SSTR1 or SSTR3. AP102 can be used for acromegaly and neuroendocrine tumors research .
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Cat. No.: HY-RS08236
Research Areas:  

Others

MCM3AP Human Pre-designed siRNA Set A contains three designed siRNAs for MCM3AP gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-RS10510
Research Areas:  

Others

PIK3AP1 Human Pre-designed siRNA Set A contains three designed siRNAs for PIK3AP1 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-RS22016
Research Areas:  

Others

Pik3ap1 Mouse Pre-designed siRNA Set A contains three designed siRNAs for Pik3ap1 gene (Mouse), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-RS28534
Research Areas:  

Others

Pik3ap1 Rat Pre-designed siRNA Set A contains three designed siRNAs for Pik3ap1 gene (Rat), as well as a negative control, a positive control, and a FAM-labeled negative control.
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Cat. No.: HY-P11606
Target:  

Porcupine Wnt

Research Areas:  

Cancer

WNT3Ap is a polypeptide corresponding to the hairpin 2 domain of the WNT3A protein. WNT3Ap undergoes palmitoylation modification catalyzed by PORCN. WNT3Ap is a key compound for elucidating the molecular mechanism of the Wnt signaling pathway and for developing PORCN inhibitors .
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Cat. No.: HY-184176
Research Areas:  

Cancer

DBCO-PEG3-AP1867 is a bifunctional molecular building block that binds to FKBP12 F36V, and also a SPAAC-compatible reagent suitable for synthesizing O-GlcNAcylation-targeting chimeras (OGTACs) against c-Myc. DBCO-PEG3-AP1867 is applicable to cancer-related research .
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Cat. No.: HY-P88754
Synonyms: BCAP

Host:  

Mouse

Application:  

IHC-P, ICC/IF, FC

Reactivity:  

Human, Mouse, Rat

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Cat. No.: HY-P88754A
Synonyms: BCAP

Host:  

Mouse

Application:  

IHC-P, ICC/IF, FC

Reactivity:  

Human, Mouse, Rat

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Cat. No.: HY-P75310
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: Hematopoietic cell signal transducer; HCST; DAP10; KAP10; PIK3AP
Species:  
Source:  
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Cat. No.: HY-P83024
Synonyms: KAP3; KIF3AP; KifAP3; Kinesin associated protein 3; SMAP

Host:  

Rabbit

Application:  

WB, IHC-P, ICC/IF, FC

Reactivity:  

Human, Mouse, Rat

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Cat. No.: HY-181500
Research Areas:  

Cancer

AP1867-NH-PEG3-acid (Compound S15) is a Target Protein Ligand-Linker Conjugate that contains the FKBP12 F36V ligand AP1867 (HY-114434) and a PROTAC linker, and recruits E3 ligase. JQ-1-Azidopropylamine is available for the synthesis of PROTAC RAFKBP12 (HY-181498) .
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