TYLOSIN LACTATE

Details

Stereochemistry	EPIMERIC
Molecular Formula	C46H77NO17.C3H6O3
Molecular Weight	1006.178
Optical Activity	UNSPECIFIED
Defined Stereocenters	21 / 22
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure Search

SMILES

CC(O)C(O)=O.CC[C@H]1OC(=O)C[C@@H](O)[C@H](C)[C@@H](O[C@@H]2O[C@H](C)[C@@H](O[C@H]3C[C@@](C)(O)[C@@H](O)[C@H](C)O3)[C@@H]([C@H]2O)N(C)C)[C@@H](CC=O)C[C@@H](C)C(=O)\C=C\C(C)=C\[C@@H]1CO[C@@H]4O[C@H](C)[C@@H](O)[C@@H](OC)[C@H]4OC

InChI

InChIKey=RYUPCWUNGWONDQ-IAGPQMRQSA-N

InChI=1S/C46H77NO17.C3H6O3/c1-13-33-30(22-58-45-42(57-12)41(56-11)37(52)26(5)60-45)18-23(2)14-15-31(49)24(3)19-29(16-17-48)39(25(4)32(50)20-34(51)62-33)64-44-38(53)36(47(9)10)40(27(6)61-44)63-35-21-46(8,55)43(54)28(7)59-35;1-2(4)3(5)6/h14-15,17-18,24-30,32-33,35-45,50,52-55H,13,16,19-22H2,1-12H3;2,4H,1H3,(H,5,6)/b15-14+,23-18+;/t24-,25+,26-,27-,28+,29+,30-,32-,33-,35+,36-,37-,38-,39-,40-,41-,42-,43+,44+,45-,46-;/m1./s1

HIDE SMILES / InChI

Molecular Formula	C3H6O3
Molecular Weight	90.0779
Charge	0
Count

Stereochemistry	RACEMIC
Additional Stereochemistry	No
Defined Stereocenters	0 / 1
E/Z Centers	0
Optical Activity	( + / - )

Molecular Formula	C46H77NO17
Molecular Weight	916.1001
Charge	0
Count

Stereochemistry	ABSOLUTE
Additional Stereochemistry	No
Defined Stereocenters	21 / 21
E/Z Centers	0
Optical Activity	UNSPECIFIED

Approval Year

Substance Class	Chemical Created by `admin` on `Mon Mar 31 23:36:07 GMT 2025` Edited by `admin` on `Mon Mar 31 23:36:07 GMT 2025`
Record UNII	V54Q4599K5
Record Status	`Validated (UNII)`
Record Version

Download

Name

Type

Language

TYLOSIN LACTATE

Common Name

English

LACTIC ACID, COMPD. WITH TYLOSIN (1:1)

Preferred Name

English

TYLOSIN, LACTATE

Common Name

English

PROPANOIC ACID, 2-HYDROXY-, COMPD. WITH TYLOSIN (1:1)

Common Name

English

TYLOSIN, LACTATE (1:1)

Common Name

English

TYLOSIN, 2-HYDROXYPROPANOATE (SALT)

Systematic Name

English

Code System Code Type Description

CAS

11034-63-2

Created by admin on Mon Mar 31 23:36:07 GMT 2025 , Edited by admin on Mon Mar 31 23:36:07 GMT 2025

PRIMARY

FDA UNII

V54Q4599K5

Created by admin on Mon Mar 31 23:36:07 GMT 2025 , Edited by admin on Mon Mar 31 23:36:07 GMT 2025

PRIMARY

PUBCHEM

6444601

Created by admin on Mon Mar 31 23:36:07 GMT 2025 , Edited by admin on Mon Mar 31 23:36:07 GMT 2025

PRIMARY

EPA CompTox

DTXSID9021423

Created by admin on Mon Mar 31 23:36:07 GMT 2025 , Edited by admin on Mon Mar 31 23:36:07 GMT 2025

PRIMARY