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Details

Stereochemistry ABSOLUTE
Molecular Formula C97H139N19O17
Molecular Weight 1843.2587
Optical Activity UNSPECIFIED
Defined Stereocenters 14 / 14
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of VALINEGRAMICIDIN B

SMILES

CC(C)C[C@@H](NC(=O)[C@H](C)NC(=O)CNC(=O)[C@@H](NC=O)C(C)C)C(=O)N[C@@H](C)C(=O)N[C@H](C(C)C)C(=O)N[C@@H](C(C)C)C(=O)N[C@H](C(C)C)C(=O)N[C@@H](CC1=CNC2=C1C=CC=C2)C(=O)N[C@H](CC(C)C)C(=O)N[C@@H](CC3=CC=CC=C3)C(=O)N[C@H](CC(C)C)C(=O)N[C@@H](CC4=CNC5=C4C=CC=C5)C(=O)N[C@H](CC(C)C)C(=O)N[C@@H](CC6=CNC7=C6C=CC=C7)C(=O)NCCO

InChI

InChIKey=LQSMEVHEYXACJP-DSHASFMGSA-N
InChI=1S/C97H139N19O17/c1-51(2)38-71(106-84(120)59(17)104-79(119)49-102-94(130)80(55(9)10)103-50-118)87(123)105-60(18)85(121)114-82(57(13)14)96(132)116-83(58(15)16)97(133)115-81(56(11)12)95(131)113-78(45-64-48-101-70-35-27-24-32-67(64)70)93(129)109-72(39-52(3)4)88(124)110-75(42-61-28-20-19-21-29-61)91(127)107-74(41-54(7)8)90(126)112-77(44-63-47-100-69-34-26-23-31-66(63)69)92(128)108-73(40-53(5)6)89(125)111-76(86(122)98-36-37-117)43-62-46-99-68-33-25-22-30-65(62)68/h19-35,46-48,50-60,71-78,80-83,99-101,117H,36-45,49H2,1-18H3,(H,98,122)(H,102,130)(H,103,118)(H,104,119)(H,105,123)(H,106,120)(H,107,127)(H,108,128)(H,109,129)(H,110,124)(H,111,125)(H,112,126)(H,113,131)(H,114,121)(H,115,133)(H,116,132)/t59-,60-,71+,72+,73+,74+,75-,76-,77-,78-,80-,81+,82+,83-/m0/s1

HIDE SMILES / InChI

Approval Year

PubMed

PubMed

TitleDatePubMed
The linear pentadecapeptide gramicidin is assembled by four multimodular nonribosomal peptide synthetases that comprise 16 modules with 56 catalytic domains.
2004 Feb 27
Name Type Language
VALINEGRAMICIDIN B
Common Name English
TRYPTOPHANAMIDE, FORMYL-L-VALYLGLYCYL-L-ALANYL-D-LEUCYL-L-ALANYL-D-VALYL-L-VALYL-D-VALYL-L-TRYPTOPHYL-D-LEUCYL-L-PHENYLALANYL-D-LEUCYL-L-TRYPTOPHYL-D-LEUCYL-N-2-HYDROXYETHYL-
Systematic Name English
GRAMICIDIN A, 1-L-VALINE-11-PHENYLALANINE
Common Name English
1-L-VALINEGRAMICIDIN B
Common Name English
Code System Code Type Description
PUBCHEM
25244501
Created by admin on Fri Dec 15 16:28:52 GMT 2023 , Edited by admin on Fri Dec 15 16:28:52 GMT 2023
PRIMARY
CAS
4422-52-0
Created by admin on Fri Dec 15 16:28:52 GMT 2023 , Edited by admin on Fri Dec 15 16:28:52 GMT 2023
PRIMARY
FDA UNII
7F82B1QV4X
Created by admin on Fri Dec 15 16:28:52 GMT 2023 , Edited by admin on Fri Dec 15 16:28:52 GMT 2023
PRIMARY