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Details

Stereochemistry ABSOLUTE
Molecular Formula C43H74N2O14.C6H10O4
Molecular Weight 989.1939
Optical Activity UNSPECIFIED
Defined Stereocenters 19 / 19
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of SPIRAMYCIN I ADIPATE

SMILES

OC(=O)CCCCC(O)=O.[H][C@@]1(C[C@@](C)(O)[C@@H](O)[C@H](C)O1)O[C@@H]2[C@@H](C)O[C@@]([H])(O[C@H]3[C@@H](CC=O)C[C@@H](C)[C@@H](O[C@@]4([H])CC[C@@H]([C@@H](C)O4)N(C)C)\C=C\C=C\C[C@@H](C)OC(=O)C[C@@H](O)[C@@H]3OC)[C@H](O)[C@H]2N(C)C

InChI

InChIKey=PLQDGTZICFBBSO-MHNXHBLWSA-N
InChI=1S/C43H74N2O14.C6H10O4/c1-24-21-29(19-20-46)39(59-42-37(49)36(45(9)10)38(27(4)56-42)58-35-23-43(6,51)41(50)28(5)55-35)40(52-11)31(47)22-33(48)53-25(2)15-13-12-14-16-32(24)57-34-18-17-30(44(7)8)26(3)54-34;7-5(8)3-1-2-4-6(9)10/h12-14,16,20,24-32,34-42,47,49-51H,15,17-19,21-23H2,1-11H3;1-4H2,(H,7,8)(H,9,10)/b13-12+,16-14+;/t24-,25-,26-,27-,28+,29+,30+,31-,32+,34+,35+,36-,37-,38-,39+,40+,41+,42+,43-;/m1./s1

HIDE SMILES / InChI

Molecular Formula C6H10O4
Molecular Weight 146.1412
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula C43H74N2O14
Molecular Weight 843.0527
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 19 / 19
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

Substance Class Chemical
Created
by admin
on Fri Dec 15 21:20:41 GMT 2023
Edited
by admin
on Fri Dec 15 21:20:41 GMT 2023
Record UNII
XH41QR4E2K
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
SPIRAMYCIN I ADIPATE
Common Name English
SPIRAMYCIN A ADIPATE
Common Name English
LEUCOMYCIN V, 9-O-(5-(DIMETHYLAMINO)TETRAHYDRO-6-METHYL-2H-PYRAN-2-YL)-, (9(5S,6R))-, HEXANEDIOATE (1:1) (SALT)
Common Name English
FOROMACIDIN A ADIPATE
Common Name English
Code System Code Type Description
CAS
23293-98-3
Created by admin on Fri Dec 15 21:20:42 GMT 2023 , Edited by admin on Fri Dec 15 21:20:42 GMT 2023
PRIMARY
PUBCHEM
146019587
Created by admin on Fri Dec 15 21:20:42 GMT 2023 , Edited by admin on Fri Dec 15 21:20:42 GMT 2023
PRIMARY
EPA CompTox
DTXSID60177863
Created by admin on Fri Dec 15 21:20:42 GMT 2023 , Edited by admin on Fri Dec 15 21:20:42 GMT 2023
PRIMARY
FDA UNII
XH41QR4E2K
Created by admin on Fri Dec 15 21:20:42 GMT 2023 , Edited by admin on Fri Dec 15 21:20:42 GMT 2023
PRIMARY
Related Record Type Details
PARENT -> SALT/SOLVATE