(1S)-2,3-DIHYDRO-1H-INDEN-1-YL ESTER [(3,4-DICHLOROPHENYL)METHYL]-CARBAMIC ACID
(1S)-2,3-DIHYDRO-1H-INDEN-1-YL ESTER [(3,4-DICHLOROPHENYL)METHYL]-CARBAMIC ACID Basic information
- Product Name:
- (1S)-2,3-DIHYDRO-1H-INDEN-1-YL ESTER [(3,4-DICHLOROPHENYL)METHYL]-CARBAMIC ACID
- Synonyms:
-
- CAY10443
- (1S)-2,3-DIHYDRO-1H-INDEN-1-YL ESTER [(3,4-DICHLOROPHENYL)METHYL]-CARBAMIC ACID
- (S)-INDAN-1-YL 3,4-DICHLOROBENZYLCARBAMATE
- CKERQCMQSBFFKX-INIZCTEOSA-N
- Carbamic acid, [(3,4-dichlorophenyl)methyl]-, (1S)-2,3-dihydro-1H-inden-1-yl ester (9CI)
- CAS:
- 582314-48-5
- MF:
- C17H15Cl2NO2
- MW:
- 336.21
- Mol File:
- Mol File
(1S)-2,3-DIHYDRO-1H-INDEN-1-YL ESTER [(3,4-DICHLOROPHENYL)METHYL]-CARBAMIC ACID Chemical Properties
- Boiling point:
- 495.6±45.0 °C(Predicted)
- Density
- 1.36±0.1 g/cm3(Predicted)
- storage temp.
- Store at -20°C
- solubility
- DMF: 30 mg/ml; DMSO: 25 mg/ml; DMSO:PBS (pH 7.2)(1:2:): .25 mg/ml; Ethanol: 5 mg/ml
- form
- A crystalline solid
- pka
- 11.15±0.46(Predicted)
(1S)-2,3-DIHYDRO-1H-INDEN-1-YL ESTER [(3,4-DICHLOROPHENYL)METHYL]-CARBAMIC ACID Usage And Synthesis
Uses
Apoptosis inducer 34 (Compound 4) is a small molecule compound that induces apoptosis by directly activating the intrinsic apoptotic pathway. Apoptosis inducer 34 promotes Apaf-1 oligomerization to form mature apoptosomes, thereby activating caspase-9 and caspase-3. It significantly activates the apoptotic pathway in Jurkat cells by enhancing the cytochrome c-dependent apoptotic signaling pathway, inducing PARP cleavage and chromosomal DNA fragmentation. Furthermore, Apoptosis inducer 34 exhibits low toxicity to normal cells, demonstrating potential for selective targeting of cancer cells. Apoptosis inducer 34 is a promising candidate for studying cancer related to apoptotic pathways[1].
Definition
ChEBI: Carbamic acid, [(3,4-dichlorophenyl)methyl]-, (1s)-2,3-dihydro-1h-inden-1-yl ester is a member of indanes.
References
[1] Nguyen JT, et al. Direct activation of the apoptosis machinery as a mechanism to target cancer cells. Proc Natl Acad Sci U S A. 2003 Jun 24;100(13):7533-8. DOI:10.1073/pnas.1031631100
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