Size | Price | |
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500mg | ||
1g | ||
Other Sizes |
ln Vitro |
ONX 0801 (BGC 945) is intended to more successfully target cancer cells that overexpress the α-FR, therefore reducing toxicity even further[1]. A431, A431-FBP, KB, IGROV-1, and JEG-3 cells have IC50 values of 6.6 μM, 1.1 nM, 3.3 nM, 90 nM, and 0.32 μM for ONX 0801 (BGC 945)[2].
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ln Vivo |
In comparison to other tissues, BGC 945 (100 mg/kg, intraperitoneal/IV injection) in the tumor had a longer half-life (28 hours)[2]. BGC 945, administered at a dose of 100 mg/kg per day for 16 days, does not cause weight loss, renal dysfunction, or macroscopic indications of toxicity to the main organs[2]. In line with tumor targeting, BGC 945 at 100 mg/kg causes a 5–20-fold increase in tumor dUrd at 4-72 hours without increasing plasma levels[2].
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Animal Protocol |
Animal/Disease Models: Mice (on the folate-free diet for 5 days were transplanted with tumor and the implants)[2] .
Doses: 100 mg/kg (pharmacokinetic/PK Analysis). Route of Administration: Single ip or iv injection. Experimental Results: After ip injection, the compound was well absorbed from the peritoneal cavity. The plasma AUC was 50% higher for ip compared with iv administration and was also higher in spleen, kidney, and liver by this route. Tumor AUC was similar via either route. |
References |
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Molecular Formula |
C32H30N5NA3O10
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Molecular Weight |
713.5774
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Exact Mass |
713.168
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CAS # |
1097638-00-0
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Related CAS # |
Idetrexed;501332-69-0
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PubChem CID |
136242346
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Appearance |
Typically exists as solid at room temperature
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Hydrogen Bond Donor Count |
4
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Hydrogen Bond Acceptor Count |
12
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Rotatable Bond Count |
12
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Heavy Atom Count |
50
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Complexity |
1290
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Defined Atom Stereocenter Count |
3
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SMILES |
C#CCN([C@H]1CCC2=CC3=C(C=C12)C(=O)NC(=N3)CO)C4=CC=C(C=C4)C(=O)N[C@@H](CCC(=O)N[C@H](CCC(=O)[O-])C(=O)[O-])C(=O)[O-].[Na+].[Na+].[Na+]
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InChi Key |
JMUBAMVCKZFETQ-GVNLSHJKSA-K
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InChi Code |
InChI=1S/C32H33N5O10.3Na/c1-2-13-37(25-10-5-18-14-24-21(15-20(18)25)30(43)36-26(16-38)33-24)19-6-3-17(4-7-19)29(42)35-23(32(46)47)8-11-27(39)34-22(31(44)45)9-12-28(40)41;;;/h1,3-4,6-7,14-15,22-23,25,38H,5,8-13,16H2,(H,34,39)(H,35,42)(H,40,41)(H,44,45)(H,46,47)(H,33,36,43);;;/q;3*+1/p-3/t22-,23+,25+;;;/m1.../s1
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Chemical Name |
trisodium;(2R)-2-[[(4S)-4-carboxylato-4-[[4-[[(6S)-2-(hydroxymethyl)-4-oxo-3,6,7,8-tetrahydrocyclopenta[g]quinazolin-6-yl]-prop-2-ynylamino]benzoyl]amino]butanoyl]amino]pentanedioate
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HS Tariff Code |
2934.99.9001
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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 | 1.4014 mL | 7.0069 mL | 14.0138 mL | |
5 mM | 0.2803 mL | 1.4014 mL | 2.8028 mL | |
10 mM | 0.1401 mL | 0.7007 mL | 1.4014 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.