| Size | Price | |
|---|---|---|
| 500mg | ||
| 1g | ||
| Other Sizes |
| ln Vitro |
Similar to Cambinol (200 μM), CHIC-35 (0.5 μM; 16 hours) also promotes histone H4 acetylation in BMDM [1]. There was no significant difference in early embryo survival observed in CHIC-35 (5 μM; 72 hours) [2]. To advance to different embryonic stages, 2.4 ng of chd7 MO was microinjected into zebrafish embryos. CHIC-35 was administered to chd7 mutant embryos between the ages of 8 and 24 hpf. After removing CHIC-35 (5 μM) at 24 hpf, the embryos were cultured in new egg water until they reached 4 dpf. Comparing chd7 amorphous larvae to controls, the pattern of cartilage elements is significantly decreased and disordered; however, CHIC-35 exhibits a partial repair of craniofacial cartilage elements [2]. At 4 dpf, the mandibles of control zebrafish embryos were well-formed, while the mandibles of chd7 mutants were smaller. Treatment with CHIC-35 (5 μM) restores the expression of the sox9ainchd7 morphant [2]. Compared to 10% of wild-type controls, over 30% of chd7 mutant embryos (24hpf to 72hpf) displayed an almost total loss of isl2a expression in the cranial region. This amount was considerably decreased to 7.5% by CHIC-35. Tg-labeled enteric neurons, however, did not exhibit any discernible effects from CHIC-35 [2].
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| References |
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| Additional Infomation |
CHIC-35 is an organoheterocyclic compound formed by the fusion of the 2-3 bond of 5-chloroindole with the 2-3 bond of cycloheptaneformamide (S enantiomer). It is a potent, cell-membrane-penetrating, metabolically stable, and selective inhibitor of the deacetylase SIRT1. It functions as an inhibitor of EC 3.5.1.98 (histone deacetylase). It is an aromatic compound, an organoheterocyclic compound, an organochlorine compound, and a primary formamide.
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| Molecular Formula |
C14H15CLN2O
|
|---|---|
| Molecular Weight |
262.74
|
| Exact Mass |
262.087
|
| CAS # |
848193-72-6
|
| PubChem CID |
914268
|
| Appearance |
Typically exists as solid at room temperature
|
| LogP |
4.266
|
| Hydrogen Bond Donor Count |
2
|
| Hydrogen Bond Acceptor Count |
1
|
| Rotatable Bond Count |
1
|
| Heavy Atom Count |
18
|
| Complexity |
336
|
| Defined Atom Stereocenter Count |
1
|
| SMILES |
NC([C@H]1CCCCC2C3C=C(Cl)C=CC=3NC1=2)=O
|
| InChi Key |
ABIVOOWWGYJNLV-JTQLQIEISA-N
|
| InChi Code |
InChI=1S/C14H15ClN2O/c15-8-5-6-12-11(7-8)9-3-1-2-4-10(14(16)18)13(9)17-12/h5-7,10,17H,1-4H2,(H2,16,18)/t10-/m0/s1
|
| Chemical Name |
(6S)-2-chloro-5,6,7,8,9,10-hexahydrocyclohepta[b]indole-6-carboxamide
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| Synonyms |
CHIC 35; CHIC35; CHIC-35
|
| HS Tariff Code |
2934.99.9001
|
| Storage |
Powder -20°C 3 years 4°C 2 years In solvent -80°C 6 months -20°C 1 month |
| Shipping Condition |
Room temperature (This product is stable at ambient temperature for a few days during ordinary shipping and time spent in Customs)
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| Solubility (In Vitro) |
May dissolve in DMSO (in most cases), if not, try other solvents such as H2O, Ethanol, or DMF with a minute amount of products to avoid loss of samples
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|---|---|
| Solubility (In Vivo) |
Note: Listed below are some common formulations that may be used to formulate products with low water solubility (e.g. < 1 mg/mL), you may test these formulations using a minute amount of products to avoid loss of samples.
Injection Formulations
Injection Formulation 1: DMSO : Tween 80： Saline = 10 : 5 : 85 (i.e. 100 μL DMSO stock solution → 50 μL Tween 80 → 850 μL Saline)(e.g. IP/IV/IM/SC) *Preparation of saline: Dissolve 0.9 g of sodium chloride in 100 mL ddH ₂ O to obtain a clear solution. Injection Formulation 2: DMSO : PEG300 ：Tween 80 : Saline = 10 : 40 : 5 : 45 (i.e. 100 μL DMSO → 400 μLPEG300 → 50 μL Tween 80 → 450 μL Saline) Injection Formulation 3: DMSO : Corn oil = 10 : 90 (i.e. 100 μL DMSO → 900 μL Corn oil) Example: Take the Injection Formulation 3 (DMSO : Corn oil = 10 : 90) as an example, if 1 mL of 2.5 mg/mL working solution is to be prepared, you can take 100 μL 25 mg/mL DMSO stock solution and add to 900 μL corn oil, mix well to obtain a clear or suspension solution (2.5 mg/mL, ready for use in animals). View More
Injection Formulation 4: DMSO : 20% SBE-β-CD in saline = 10 : 90 [i.e. 100 μL DMSO → 900 μL (20% SBE-β-CD in saline)] Oral Formulations
Oral Formulation 1: Suspend in 0.5% CMC Na (carboxymethylcellulose sodium) Oral Formulation 2: Suspend in 0.5% Carboxymethyl cellulose Example: Take the Oral Formulation 1 (Suspend in 0.5% CMC Na) as an example, if 100 mL of 2.5 mg/mL working solution is to be prepared, you can first prepare 0.5% CMC Na solution by measuring 0.5 g CMC Na and dissolve it in 100 mL ddH2O to obtain a clear solution; then add 250 mg of the product to 100 mL 0.5% CMC Na solution, to make the suspension solution (2.5 mg/mL, ready for use in animals). View More
Oral Formulation 3: Dissolved in PEG400 (Please use freshly prepared in vivo formulations for optimal results.) |
| Preparing Stock Solutions | 1 mg | 5 mg | 10 mg | |
| 1 mM | 3.8060 mL | 19.0302 mL | 38.0604 mL | |
| 5 mM | 0.7612 mL | 3.8060 mL | 7.6121 mL | |
| 10 mM | 0.3806 mL | 1.9030 mL | 3.8060 mL |
*Note: Please select an appropriate solvent for the preparation of stock solution based on your experiment needs. For most products, DMSO can be used for preparing stock solutions (e.g. 5 mM, 10 mM, or 20 mM concentration); some products with high aqueous solubility may be dissolved in water directly. Solubility information is available at the above Solubility Data section. Once the stock solution is prepared, aliquot it to routine usage volumes and store at -20°C or -80°C. Avoid repeated freeze and thaw cycles.
Calculation results
Working concentration： mg/mL；
Method for preparing DMSO stock solution： mg drug pre-dissolved in μL DMSO (stock solution concentration mg/mL). Please contact us first if the concentration exceeds the DMSO solubility of the batch of drug.
Method for preparing in vivo formulation:：Take μL DMSO stock solution, next add μL PEG300, mix and clarify, next addμL Tween 80, mix and clarify, next add μL ddH2O，mix and clarify.
(1) Please be sure that the solution is clear before the addition of next solvent. Dissolution methods like vortex, ultrasound or warming and heat may be used to aid dissolving.
(2) Be sure to add the solvent(s) in order.
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