Elinafide
CAS No. 162706-37-8
Elinafide( —— )
Catalog No. M36163 CAS No. 162706-37-8
Elinafide, a dinaphthylimide cytotoxic agent, is a DNA-targeted anticancer agent that has shown antitumor activity in in vitro and in vivo assays.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 5MG | 39 | In Stock |
|
| 10MG | 61 | In Stock |
|
| 25MG | 115 | In Stock |
|
| 50MG | 155 | In Stock |
|
| 100MG | 222 | In Stock |
|
| 200MG | 312 | In Stock |
|
| 500MG | Get Quote | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
-
Product NameElinafide
-
NoteResearch use only, not for human use.
-
Brief DescriptionElinafide, a dinaphthylimide cytotoxic agent, is a DNA-targeted anticancer agent that has shown antitumor activity in in vitro and in vivo assays.
-
DescriptionElinafide, a dinaphthylimide cytotoxic agent, is a DNA-targeted anticancer agent that has shown antitumor activity in in vitro and in vivo assays.
-
In Vitro——
-
In Vivo——
-
Synonyms——
-
PathwayCell Cycle/DNA Damage
-
TargetDNA/RNA Synthesis
-
RecptorDNA
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number162706-37-8
-
Formula Weight520.58
-
Molecular FormulaC31H28N4O4
-
Purity>98% (HPLC)
-
Solubility——
-
SMILESO=C1C=2C=3C(C(=O)N1CCNCCCNCCN4C(=O)C=5C=6C(C4=O)=CC=CC6C=CC5)=CC=CC3C=CC2
-
Chemical Name——
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
molnova catalog
related products
-
1,4-Dideoxy-1,4-epit...
1,4-Dideoxy-1,4-epithio-D-ribitol is a purine nucleoside analog that targets malignant tumors of the inert lymphatic system and possesses a broad spectrum of antitumor activity.1,4-Dideoxy-1,4-epithio-D-ribitol induces apoptosis through inhibition of DNA synthesis.
-
Apricitabine
Apricitabine (SPD754) is a highly selective and orally active HIV-1 reverse transcriptase inhibitor (Ki=0.08 μM), the (-) enantiomer of 2′-deoxy-3′-oxy-4′-thiocytidine (dOTC) .
-
ZM 39923 hydrochlori...
ZM 39923 hydrochloride is a JAK1/3 inhibitor with pIC50 of 4.4/7.1, almost no activity to JAK2 and modestly potent to EGFR; also found to be sensitive to transglutaminase.
Cart
sales@molnova.com