Secorapamycin Na salt

Product Name Secorapamycin Na salt
Alternate Names Rapamycin Impurities, Impurities of Rapamycin
CAT No. CS-T-85121
CAS No. 148554-65-8
Category Impurities
Stock IN-Stock
Mol. Wt. 936.15 g/mol
Mol. For. C51H78NNaO13
Hazardous This is not a Hazardous Compound
COA View Sample COA
MSDS View Sample MSDS
Parent API Rapamycin
Purity 95%
Therapeutic Antibiotics
Smileys O=C([C@H]1N(C(C([C@@]2(O)[C@H](C)CC[C@@H](C[C@H](OC)/C(C)=C/C=C/C=C/[C@@H](C)C[C@@H](C)C([C@H](OC)[C@H](O)/C(C)=C/[C@@H](C)C(/C=C/[C@H](C)C[C@H]3C[C@@H](OC)[C@H](O)CC3)=O)=O)O2)=O)=O)CCCC1)[O-].[Na+]
Canonical Smiles CC1CCC(OC1(C(=O)C(=O)N2CCCCC2C(=O)[O-])O)CC(C(=CC=CC=CC(C)CC(C)C(=O)C(C(C(=CC(C)C(=O)C=CC(C)CC3CCC(C(C3)OC)O)C)O)OC)C)OC.[Na+]
InchIKey DNMSBJYMPJMFNS-OWGFPTNRSA-M
Inchl InChI=1S/C51H79NO13.Na/c1-31(26-35(5)45(55)47(64-10)46(56)36(6)28-34(4)41(53)23-19-32(2)27-38-21-24-42(54)44(29-38)63-9)16-12-11-13-17-33(3)43(62-8)30-39-22-20-37(7)51(61,65-39)48(57)49(58)52-25-15-14-18-40(52)50(59)60;/h11-13,16-17,19,23,28,31-32,34-35,37-40,42-44,46-47,54,56,61H,14-15,18,20-22,24-27,29-30H2,1-10H3,(H,59,60);/q;+1/p-1/b13-11+,16-12+,23-19+,33-17+,36-28+;/t31-,32+,34-,35-,37-,38+,39+,40+,42-,43+,44-,46-,47+,51-;/m1./s1
IUPAC sodium;(2S)-1-[2-[(2R,3R,6S)-2-hydroxy-6-[(2S,3E,5E,7E,9S,11R,13R,14R,15E,17R,19E,21R)-14-hydroxy-22-[(1S,3R,4R)-4-hydroxy-3-methoxycyclohexyl]-2,13-dimethoxy-3,9,11,15,17,21-hexamethyl-12,18-dioxodocosa-3,5,7,15,19-pentaenyl]-3-methyloxan-2-yl]-2-oxoacetyl]piperidine-2-carboxylate
Controlled No
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Secorapamycin Na salt is an antibiotic compound that belongs to the family of aminocyclitol antibiotics. This compound is derived from the bacterium Actinoplanes sp. SE50/110, and is known for its potent antibacterial activity against both Gram-negative and Gram-positive bacteria. The mechanism of action of Secorapamycin Na salt involves the inhibition of bacterial protein synthesis by binding to the 70S ribosome. The chemical structure of Secorapamycin Na salt consists of a cyclohexane ring with five hydroxyl groups attached to it, along with an aminocyclitol moiety. The compound is soluble in water and has a molecular weight of 548.57 g/mol. The usage of Secorapamycin Na salt is primarily in the treatment of bacterial infections. It has been found to be effective against a wide range of bacterial pathogens, including Staphylococcus aureus, Streptococcus pneumoniae, Klebsiella pneumoniae, and Escherichia coli. The compound is typically administered intravenously or orally, depending on the severity of the infection and the patient's condition. In conclusion, Secorapamycin Na salt is a potent antibiotic compound that has shown great promise in the treatment of bacterial infections. Its mechanism of action, chemical structure, and usage make it an important tool in the fight against antibiotic-resistant bacteria.

Related Compounds

Rapamycin Impurity 4 (Sirolimus-31,42-Diester Impurity) | Rapamycin 31,42-Bis(2,2,5-trimethyl-1,3-dioxane-5-carboxylate) | Rapamycin Dialdehyde | Rapamycin Impurity 5 (Seco Rapamycin) | Rapamycin Impurity 1 | Rapamycin Impurity 12 |

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