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500mg | ||
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Purity: ≥98%
Discovered by a Japanese group, A 17002 C is a new metabolite produced by Actinoplanes strains, structurally related to the virginiamycin factor M. On the basis of physico-chemical data, MS, IR, 1H and 13C NMR, structure I is assigned to A 17002 C.
ln Vitro |
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ln Vivo |
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Animal Protocol |
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References |
J Antibiot (Tokyo).1979 Feb;32(2):108-14.
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Molecular Formula |
C26H37N3O6
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Molecular Weight |
487.58848
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Exact Mass |
487.268
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CAS # |
71843-98-6
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Related CAS # |
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PubChem CID |
6443619
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Appearance |
Typically exists as solid at room temperature
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LogP |
3.155
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Hydrogen Bond Donor Count |
3
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Hydrogen Bond Acceptor Count |
7
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Rotatable Bond Count |
1
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Heavy Atom Count |
35
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Complexity |
822
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Defined Atom Stereocenter Count |
4
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SMILES |
OC1CC2=NC(=CO2)C(=O)NC(C)C(=O)OC(C(C)C)C(C)C=CC(=O)NCC=CC(C)=CCC1 |c:32,t:23,29|
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InChi Key |
HYYZDUUXSSRJQZ-YIBNVXJJSA-N
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InChi Code |
InChI=1S/C26H37N3O6/c1-16(2)24-18(4)11-12-22(31)27-13-7-9-17(3)8-6-10-20(30)14-23-29-21(15-34-23)25(32)28-19(5)26(33)35-24/h7-9,11-12,15-16,18-20,24,30H,6,10,13-14H2,1-5H3,(H,27,31)(H,28,32)/b9-7-,12-11-,17-8-/t18-,19-,20+,24-/m1/s1
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Chemical Name |
(4R,7R,8R,9Z,14Z,16Z,20S)-20-hydroxy-4,8,16-trimethyl-7-propan-2-yl-6,23-dioxa-3,12,25-triazabicyclo[20.2.1]pentacosa-1(24),9,14,16,22(25)-pentaene-2,5,11-trione
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Synonyms |
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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 |
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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) |
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Solubility (In Vivo) |
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Preparing Stock Solutions | 1 mg | 5 mg | 10 mg | |
1 mM | 2.0509 mL | 10.2545 mL | 20.5090 mL | |
5 mM | 0.4102 mL | 2.0509 mL | 4.1018 mL | |
10 mM | 0.2051 mL | 1.0255 mL | 2.0509 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.