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Neamine tetrahydrochloride 15446-43-2

Neamine tetrahydrochloride 15446-43-2

CAS No.: 15446-43-2

Neamine tetra HCl, a degradation product of neomycin, is a broad-spectrum aminoglycoside antibiotic. Neamine tetra HCl i
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Neamine tetra HCl, a degradation product of neomycin, is a broad-spectrum aminoglycoside antibiotic. Neamine tetra HCl is an anti-angiogenic agent targeting angiogenin. Neamine tetra HCl has potent antibacterial, antitumor and neuro-protection activities.

Physicochemical Properties


Molecular Formula C12H30CL4N4O6
Molecular Weight 468.20
Exact Mass 466.092
CAS # 15446-43-2
Related CAS # Neamine;3947-65-7
PubChem CID 11784617
Appearance White to off-white solid powder
LogP 0.893
Hydrogen Bond Donor Count 12
Hydrogen Bond Acceptor Count 10
Rotatable Bond Count 3
Heavy Atom Count 26
Complexity 378
Defined Atom Stereocenter Count 10
SMILES

NCC1O[C@H](O[C@@H]2C(N)C[C@@H](N)C(O)[C@H]2O)C(N)[C@@H](O)[C@@H]1O

InChi Key YHGAXELMYJIVJN-OXGCEHIISA-N
InChi Code

InChI=1S/C12H26N4O6.4ClH/c13-2-5-8(18)9(19)6(16)12(21-5)22-11-4(15)1-3(14)7(17)10(11)20;;;;/h3-12,17-20H,1-2,13-16H2;4*1H/t3-,4+,5-,6-,7+,8-,9-,10-,11-,12-;;;;/m1..../s1
Chemical Name

(2R,3S,4R,5R,6R)-5-amino-2-(aminomethyl)-6-[(1R,2R,3S,4R,6S)-4,6-diamino-2,3-dihydroxycyclohexyl]oxyoxane-3,4-diol;tetrahydrochloride
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)

Biological Activity


ln Vitro Neamine treatment (0.625-25 μM; 48 hours; AsPC-1 cells) dose-dependently suppresses the proliferation of ANG-mediated AsPC-1 cells in the range of 0.625-25 μM[1]. Neamine (100 μM) also successfully prevents ANG from translocating nuclear[1].
ln Vivo In AsPC-1 xenograft models, neamine (30–60 mg/kg; subcutaneous injection; daily; for 14 days; male Balb/c nude mice) has anti-tumor properties. In tumor xenografts, neamine lowers the expression levels of ANG, Ki-67, and CD31[1].
Cell Assay Cell Proliferation Assay[1]
Cell Types: AsPC-1 cells
Tested Concentrations: 0.625 µM, 1.25 µM, 2.5 µM, 5 µM, 10 µM, 25 µM
Incubation Duration: 48 hrs (hours)
Experimental Results: Inhibited angiogenin (ANG)-induced AsPC-1 cells proliferation.
Animal Protocol Animal/Disease Models: Male Balb/c nude mice (4 weeks old) injected with AsPC-1 cells[1]
Doses: 30 mg/kg, 60 mg/kg
Route of Administration: subcutaneous (sc)injection; daily; for 14 days
Experimental Results: Had anti-tumor effects on AsPC-1 xenograft models.
References

[1]. Neamine Inhibits Growth of Pancreatic Cancer Cells in Vitro and in Vivo. J Huazhong Univ Sci Technolog Med Sci. 2016 Feb;36(1):82-87.

[2]. Neamine Induces Neuroprotection After Acute Ischemic Stroke in Type One Diabetic Rats. Neuroscience. 2014 Jan 17;257:76-85.


Solubility Data


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
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
(e.g. IP/IV/IM/SC)
Injection Formulation 1: DMSO : Tween 80: Saline = 10 : 5 : 85 (i.e. 100 μL DMSO stock solution 50 μL Tween 80 850 μL Saline)
*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).
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)]
*Preparation of 20% SBE-β-CD in Saline (4°C,1 week): Dissolve 2 g SBE-β-CD in 10 mL saline to obtain a clear solution.
Injection Formulation 5: 2-Hydroxypropyl-β-cyclodextrin : Saline = 50 : 50 (i.e. 500 μL 2-Hydroxypropyl-β-cyclodextrin 500 μL Saline)
Injection Formulation 6: DMSO : PEG300 : castor oil : Saline = 5 : 10 : 20 : 65 (i.e. 50 μL DMSO 100 μLPEG300 200 μL castor oil 650 μL Saline)
Injection Formulation 7: Ethanol : Cremophor : Saline = 10: 10 : 80 (i.e. 100 μL Ethanol 100 μL Cremophor 800 μL Saline)
Injection Formulation 8: Dissolve in Cremophor/Ethanol (50 : 50), then diluted by Saline
Injection Formulation 9: EtOH : Corn oil = 10 : 90 (i.e. 100 μL EtOH 900 μL Corn oil)
Injection Formulation 10: EtOH : PEG300:Tween 80 : Saline = 10 : 40 : 5 : 45 (i.e. 100 μL EtOH 400 μLPEG300 50 μL Tween 80 450 μL 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).
Oral Formulation 3: Dissolved in PEG400
Oral Formulation 4: Suspend in 0.2% Carboxymethyl cellulose
Oral Formulation 5: Dissolve in 0.25% Tween 80 and 0.5% Carboxymethyl cellulose
Oral Formulation 6: Mixing with food powders

Note: Please be aware that the above formulations are for reference only. InvivoChem strongly recommends customers to read literature methods/protocols carefully before determining which formulation you should use for in vivo studies, as different compounds have different solubility properties and have to be formulated differently.

 (Please use freshly prepared in vivo formulations for optimal results.)
Preparing Stock Solutions 1 mg 5 mg 10 mg
1 mM 2.1358 mL 10.6792 mL 21.3584 mL
5 mM 0.4272 mL 2.1358 mL 4.2717 mL
10 mM 0.2136 mL 1.0679 mL 2.1358 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.