| Size | Price | Stock | Qty |
|---|---|---|---|
| 1mg |
|
||
| Other Sizes |
| Targets |
Protein kinase C (PKC) and other ingenol targets.
|
|---|---|
| ln Vitro |
In vitro, ingenol derivatives are known to activate protein kinase C (PKC) and exhibit various biological activities including anticancer and antiviral effects. As a protected ingenol derivative, 5,20-acetonide may be used as a precursor for bioactive ingenol derivatives. Quantitative in vitro activity data is not detailed in publicly available sources.
|
| ln Vivo |
In vivo activity data is not publicly available. As a synthetic intermediate, it is not typically used directly in animal studies.
|
| Enzyme Assay |
No specific cell-free assay protocol is detailed for this compound. For ingenol derivatives, typical cell-free assays include PKC activation assays using purified PKC and synthetic substrates, or receptor binding studies.
|
| Cell Assay |
Cellular activity is assessed in cell lines to study PKC activation and downstream signaling. Cells are treated with the compound or its deprotected derivatives, and endpoints include PKC activity assays, phosphorylation of PKC substrates, and cell viability.
|
| Animal Protocol |
No in vivo animal experimental protocol is publicly available for this compound.
|
| ADME/Pharmacokinetics |
Molecular weight and formula are not readily available in public sources. Storage: typical for organic compounds (desiccated, protected from light, -20°C).
|
| Toxicity/Toxicokinetics |
No toxicity data is publicly available.
|
| Additional Infomation |
Ingenol-5,20-acetonide is a research-grade compound used as a synthetic intermediate for ingenol derivatives. It is not approved for therapeutic use. It is used in medicinal chemistry research for the synthesis of ingenol-based drugs.
|
| Molecular Formula |
C23H32O5
|
|---|---|
| Molecular Weight |
388.4972
|
| Exact Mass |
388.224
|
| CAS # |
77573-43-4
|
| PubChem CID |
68027217
|
| Appearance |
White to off-white solid powder
|
| Density |
1.3±0.1 g/cm3
|
| Boiling Point |
531.4±50.0 °C at 760 mmHg
|
| Flash Point |
180.5±23.6 °C
|
| Vapour Pressure |
0.0±3.2 mmHg at 25°C
|
| Index of Refraction |
1.593
|
| LogP |
4.24
|
| Hydrogen Bond Donor Count |
2
|
| Hydrogen Bond Acceptor Count |
5
|
| Rotatable Bond Count |
0
|
| Heavy Atom Count |
28
|
| Complexity |
823
|
| Defined Atom Stereocenter Count |
8
|
| SMILES |
C[C@@H]1C[C@@H]2[C@@H](C2(C)C)[C@@H]3C=C4COC(O[C@H]4[C@]5([C@@]1(C3=O)C=C([C@@H]5O)C)O)(C)C
|
| InChi Key |
ONMDPPVVEFWDOD-DVBBJZJXSA-N
|
| InChi Code |
InChI=1S/C23H32O5/c1-11-9-22-12(2)7-15-16(20(15,3)4)14(18(22)25)8-13-10-27-21(5,6)28-19(13)23(22,26)17(11)24/h8-9,12,14-17,19,24,26H,7,10H2,1-6H3/t12-,14+,15-,16+,17+,19-,22+,23-/m1/s1
|
| Chemical Name |
(1S,4S,5R,6R,13S,14R,16R,18R)-4,5-dihydroxy-3,8,8,15,15,18-hexamethyl-7,9-dioxapentacyclo[11.5.1.01,5.06,11.014,16]nonadeca-2,11-dien-19-one
|
| 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)
|
| Solubility (In Vitro) |
DMSO : ~50 mg/mL (~128.70 mM)
|
|---|---|
| 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 | 2.5740 mL | 12.8700 mL | 25.7400 mL | |
| 5 mM | 0.5148 mL | 2.5740 mL | 5.1480 mL | |
| 10 mM | 0.2574 mL | 1.2870 mL | 2.5740 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.
Products are for research use only; We do not sell to patients
Copyright 2020 InvivoChem LLC | All Rights Reserved
