11 Results for "

Ifosfamide-d4

" in MedChemExpress (MCE) Product Catalog:
Products (11)

11 Results for "Ifosfamide-d4" in MCE Product Catalog:

1
1 Cited Publications
製品番号: HY-P1103
CAS 番号: 1030384-98-5
Target:  

CXCR

研究分野:  

Cancer

CTCE-9908 is a potent and selective CXCR4 antagonist. CTCE-9908 induces mitotic catastrophe, cytotoxicity and inhibits migration in CXCR4-expressing ovarian cancer cells .
製品番号: HY-P4070
CAS 番号: 1188379-43-2
Target:  

Insulin Receptor

研究分野:  

Metabolic Disease

Insulin icodec is an Insulin (HY-P0035) analog that strongly but reversibly binds to albumin. Insulin icodec has long plasma half-life. Insulin icodec modulates insulin receptor activity, controls blood glucose levels, reduces HbA1c levels, and binds reversibly to human serum albumin. Insulin icodec can be used for the research of type 2 diabetes mellitus .
製品番号: HY-17419S1
CAS 番号: 1189701-13-0
Ifosfamide-d4 is the deuterium labeled Ifosfamide. Ifosfamide is an alkylating chemotherapeutic agent with activity against a wide range of tumors .
製品番号: HY-17419S
CAS 番号: 1329497-14-4
2’-Oxo Ifosfamide-d4 is the deuterium labeled Ifosfamide. Ifosfamide is an alkylating chemotherapeutic agent with activity against a wide range of tumors .
製品番号: HY-17419S2
CAS 番号: 2012598-80-8
Ifosfamide-d4-1 is deuterium-labeled Ifosfamide (HY-17419) .
製品番号: HY-P1103A
Target:  

CXCR

研究分野:  

Cancer

CTCE-9908 TFA is a potent and selective CXCR4 antagonist. CTCE-9908 TFA induces mitotic catastrophe, cytotoxicity and inhibits migration in CXCR4-expressing ovarian cancer cells .
製品番号: HY-P11293
CAS 番号: 1309855-53-5
Target:  

Melanocortin Receptor

研究分野:  

Cancer

DOTA-GGNle-CycMSHhex is a melanocortin-1 receptor (MC1R)-targeting peptide that can be radionuclide-labeled for melanoma imaging .
製品番号: HY-P4757
CAS 番号: 108081-77-2
Target:  

Parasite

研究分野:  

Others

N1-Glutathionyl-spermidine disulfide is a substrate of trypanothione reductase .
製品番号: HY-P1321
CAS 番号: 158859-98-4
別名: 1229U91; GW1229
研究分野:  

Neurological Disease

GR231118, an analogue of the C-terminus of neuropeptide Y, is a potent , competitive and relative seletive antagonist at human neuropeptide Y Y receptor with a pKi of 10.4. GR231118 a potent agonist at the human neuropeptide Y Y4 receptor (pEC50=8.6; pKi=9.6) and a weak agonist at the human and rat neuropeptide YY2 and Y5 receptors. GR231118 also has high affinity for the mouse neuropeptide Y Y6 receptor (pKi= 8.8) .
製品番号: HY-P1321A
別名: 1229U91 TFA; GW1229 TFA
研究分野:  

Neurological Disease

GR231118 TFA, an analogue of the C-terminus of neuropeptide Y, is a potent , competitive and relative seletive antagonist at human neuropeptide YY receptor with a pKi of 10.4. GR231118 a potent agonist at the human neuropeptide YY4 receptor (pEC50=8.6; pKi=9.6) and a weak agonist at the human and rat neuropeptide Y Y2 and Y5 receptors. GR231118 also has high affinity for the mouse neuropeptide YY6 receptor (pKi= 8.8) .
製品番号: HY-P11480
CAS 番号: 3105660-96-3
Target:  

Trk Receptor

研究分野:  

Neurological Disease

TrkA/NGF-IN-1 (Peptide 19) is an inhibitor of protein-protein interactions between TrkA and NGF (IC50: 21 nM for human TrkA in PathHunter assay). TrkA/NGF-IN-1 shows an analgesic effect in a rat incisional pain model .
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