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CAS 155761-99-2

:

ranalexin

Description:
Ranalexin, with the CAS number 155761-99-2, is a chemical compound that belongs to the class of antibiotics known as phenylpyrrole derivatives. It is primarily recognized for its antifungal properties, making it useful in agricultural applications, particularly in the protection of crops against fungal pathogens. The compound exhibits a mechanism of action that disrupts fungal cell wall synthesis, leading to cell lysis and death of the pathogen. Ranalexin is characterized by its moderate solubility in water and its stability under various environmental conditions, which enhances its effectiveness as a fungicide. Additionally, it has been studied for its potential impact on non-target organisms, emphasizing the importance of understanding its environmental behavior and toxicity. Overall, ranalexin represents a significant advancement in the development of targeted agricultural chemicals aimed at improving crop health and yield while minimizing ecological disruption.
Formula:C97H167N23O22S3
InChI:InChI=1/C97H167N23O22S3/c1-19-55(12)76(118-88(132)68(45-52(6)7)106-73(123)48-102-72(122)47-103-83(127)67(44-51(4)5)111-82(126)62(101)46-61-32-23-22-24-33-61)92(136)109-65(36-27-30-41-100)86(130)117-78(57(14)21-3)94(138)115-75(54(10)11)96(140)120-42-31-37-71(120)90(134)105-58(15)80(124)107-66(38-43-143-18)87(131)116-77(56(13)20-2)93(137)112-69-49-144-145-50-70(97(141)142)113-85(129)63(34-25-28-39-98)108-84(128)64(35-26-29-40-99)110-95(139)79(60(17)121)119-91(135)74(53(8)9)114-81(125)59(16)104-89(69)133/h22-24,32-33,51-60,62-71,74-79,121H,19-21,25-31,34-50,98-101H2,1-18H3,(H,102,122)(H,103,127)(H,104,133)(H,105,134)(H,106,123)(H,107,124)(H,108,128)(H,109,136)(H,110,139)(H,111,126)(H,112,137)(H,113,129)(H,114,125)(H,115,138)(H,116,131)(H,117,130)(H,118,132)(H,119,135)(H,141,142)/t55-,56-,57-,58-,59-,60?,62-,63-,64-,65-,66-,67-,68-,69-,70-,71-,74-,75-,76-,77-,78-,79-/m0/s1
SMILES:CC[C@H](C)[C@@H](C(=N[C@@H](CCCCN)C(=N[C@@H]([C@@H](C)CC)C(=N[C@@H](C(C)C)C(=O)N1CCC[C@H]1C(=N[C@@H](C)C(=N[C@@H](CCSC)C(=N[C@@H]([C@@H](C)CC)C(=N[C@H]1CSSC[C@@H](C(=O)O)N=C([C@H](CCCCN)N=C([C@H](CCCCN)N=C([C@H](C(C)O)N=C([C@H](C(C)C)N=C([C@H](C)N=C1O)O)O)O)O)O)O)O)O)O)O)O)O)N=C([C@H](CC(C)C)N=C(CN=C(CN=C([C@H](CC(C)C)N=C([C@H](Cc1ccccc1)N)O)O)O)O)O
Synonyms:
  • H-Phe-Leu-Gly-Gly-Leu-Ile-Lys-Ile-Val-Pro-Ala-Met-Ile-Cys-Ala-Val-Thr-Lys-Lys-Cys-OH (Disulfide bond)
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