K-7174
- Product Name
- K-7174
- CAS No.
- 191089-59-5
- Chemical Name
- K-7174
- Synonyms
- K-7174;K7174; K 7174;K-7174(FREE BASE);K-7174,K 7174,inhibit,K7174,Inhibitor;1,4-Bis((E)-5-(3,4,5-trimethoxyphenyl)pent-4-en-1-yl)-1,4-diazepane , K-7174;1H-1,4-Diazepine, hexahydro-1,4-bis[(4E)-5-(3,4,5-trimethoxyphenyl)-4-penten-1-yl]-
- CBNumber
- CB32731080
- Molecular Formula
- C33H48N2O6
- Formula Weight
- 568.74
- MOL File
- 191089-59-5.mol
K-7174 Property
- Boiling point:
- 689.9±55.0 °C(Predicted)
- Density
- 1.074±0.06 g/cm3(Predicted)
- storage temp.
- 2-8°C
- pka
- 9.60±0.10(Predicted)
- form
- Oil
- color
- Colorless to light yellow
N-Bromosuccinimide Price
- Product number
- orb611722
- Product name
- K-7174
- Packaging
- 10mg
- Price
- $324.7
- Updated
- 2021/12/16
- Product number
- orb611722
- Product name
- K-7174
- Packaging
- 50mg
- Price
- $569.5
- Updated
- 2021/12/16
- Product number
- CD31002841
- Product name
- K-7174
- Purity
- 98+%
- Packaging
- 5mg
- Price
- $76
- Updated
- 2021/12/16
- Product number
- CD31002841
- Product name
- K-7174
- Purity
- 98+%
- Packaging
- 10mg
- Price
- $115
- Updated
- 2021/12/16
- Product number
- DC23944
- Product name
- K-7174
- Purity
- >98%
- Packaging
- 10mg
- Price
- $120
- Updated
- 2021/12/16
K-7174 Chemical Properties,Usage,Production
Uses
K-7174 is an orally active proteasome and GATA inhibitor. K-7174 is a cell adhesion inhibitor. K-7174 induces cell apoptosis. K-7174 shows antitumor activities, it can be used for the research of cancer[1][2][3].
in vivo
K-7174 (30 mg/kg; i.p. once daily for 9 days) reverses the decreasing of hemoglobin concentrations and reticulocyte counts by IL-1β or TNF-α[2]. K-7174 (75 mg/kg; i.p. once daily for 14 days) inhibits the tumor growth in vivo[3]. K-7174 (50 mg/kg; p.o. once daily for 14 days) inhibits the tumor growth in vivo and shows a better effect than intraperitoneal injection[3].
| Animal Model: | ICR mice with IL-β or TNF-α injection[2] |
| Dosage: | 30 mg/kg |
| Administration: | Intraperitoneal injection; 30 mg/kg once daily for 9 days |
| Result: | Increased erythropoietin (Epo) production, reticulocyte counts, and hemoglobin (Hb) concentrations |
| Animal Model: | NOD/SCID mice with murine xenograft[3] |
| Dosage: | 75 mg/kg |
| Administration: | Intraperitoneal injection; once daily for 14 days |
| Result: | Significantly decreased tumor volume, but showed a significant body weight reduction after 10 days. |
| Animal Model: | NOD/SCID mice with murine xenograft[3] |
| Dosage: | 50 mg/kg |
| Administration: | Oral gavage; once daily for 14 days |
| Result: | Showed an anti-myeloma activity. Proved oral administration is more effective than intraperitoneal injection. |
References
[1] Umetani M, et al. A novel cell adhesion inhibitor, K-7174, reduces the endothelial VCAM-1 induction by inflammatory cytokines, acting through the regulation of GATA. Biochem Biophys Res Commun. 2000 Jun 7;272(2):370-4. DOI:10.1006/bbrc.2000.2784
[2] Imagawa S, et al. A GATA-specific inhibitor (K-7174) rescues anemia induced by IL-1beta, TNF-alpha, or L-NMMA. FASEB J. 2003 Sep;17(12):1742-4. DOI:10.1096/fj.02-1134fje
[3] Kikuchi J, et al. The novel orally active proteasome inhibitor K-7174 exerts anti-myeloma activity in vitro and in vivo by down-regulating the expression of class I histone deacetylases. J Biol Chem. 2013 Aug 30;288(35):25593-602. DOI:10.1074/jbc.M113.480574
K-7174 Preparation Products And Raw materials
Raw materials
Preparation Products
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