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Details

Stereochemistry UNKNOWN
Molecular Formula C26H36N2O4.2C3H6O3
Molecular Weight 620.7309
Optical Activity UNSPECIFIED
Defined Stereocenters 2 / 4
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of BISOBRIN LACTATE

SMILES

CC(O)C(O)=O.CC(O)C(O)=O.COC1=CC2=C(C=C1OC)[C@@H](CCCC[C@@H]3NCCC4=C3C=C(OC)C(OC)=C4)NCC2

InChI

InChIKey=IDVAETAVFSWBDA-WANFXGKWSA-N
InChI=1S/C26H36N2O4.2C3H6O3/c1-29-23-13-17-9-11-27-21(19(17)15-25(23)31-3)7-5-6-8-22-20-16-26(32-4)24(30-2)14-18(20)10-12-28-22;2*1-2(4)3(5)6/h13-16,21-22,27-28H,5-12H2,1-4H3;2*2,4H,1H3,(H,5,6)/t21-,22+;;

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 C26H36N2O4
Molecular Weight 440.575
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 2 / 2
E/Z Centers 0
Optical Activity UNSPECIFIED

PubMed

PubMed

TitleDatePubMed
[Mechanism of action of certain fibrinolytic bis-tetrahydroisoquinolines: their antagonists and histamine- and 5-hydroxytryptamine-releasing effects (author's transl)].
1980-01
Patents

Patents

Substance Class Chemical
Created
by admin
on Mon Mar 31 18:43:08 GMT 2025
Edited
by admin
on Mon Mar 31 18:43:08 GMT 2025
Record UNII
944X72NZMV
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
BISOBRIN LACTATE
USAN  
USAN  
Official Name English
ISOQUINOLINE, 1,1'-(1,4-BUTANEDIYL)BIS(1,2,3,4-TETRAHYDRO-6,7-DIMETHOXY-, (1R,1'S)-REL-, 2-HYDROXYPROPANOATE (1:2)
Preferred Name English
BISOBRIN LACTATE [USAN]
Common Name English
EN-1661L
Code English
PROPANOIC ACID, 2-HYDROXY-, COMPD. WITH (R*,S*)-1,1'-(1,4-BUTANEDIYL)BIS(1,2,3,4-TETRAHYDRO-6,7-DIMETHOXYISOQUINOLINE) (2:1)
Common Name English
MESO-1,1'-TETRAMETHYLENEBIS(1,2,3,4-TETRAHYDRO-6,7-DIMETHOXYISOQUINOLINE) DILACTATE
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C78311
Created by admin on Mon Mar 31 18:43:08 GMT 2025 , Edited by admin on Mon Mar 31 18:43:08 GMT 2025
Code System Code Type Description
ChEMBL
CHEMBL2110644
Created by admin on Mon Mar 31 18:43:08 GMT 2025 , Edited by admin on Mon Mar 31 18:43:08 GMT 2025
PRIMARY
PUBCHEM
3037066
Created by admin on Mon Mar 31 18:43:08 GMT 2025 , Edited by admin on Mon Mar 31 18:43:08 GMT 2025
PRIMARY
SMS_ID
300000055222
Created by admin on Mon Mar 31 18:43:08 GMT 2025 , Edited by admin on Mon Mar 31 18:43:08 GMT 2025
PRIMARY
NCI_THESAURUS
C142960
Created by admin on Mon Mar 31 18:43:08 GMT 2025 , Edited by admin on Mon Mar 31 18:43:08 GMT 2025
PRIMARY
CAS
22407-75-6
Created by admin on Mon Mar 31 18:43:08 GMT 2025 , Edited by admin on Mon Mar 31 18:43:08 GMT 2025
NON-SPECIFIC STOICHIOMETRY
CAS
23256-05-5
Created by admin on Mon Mar 31 18:43:08 GMT 2025 , Edited by admin on Mon Mar 31 18:43:08 GMT 2025
NON-SPECIFIC STEREOCHEMISTRY
CAS
24233-80-5
Created by admin on Mon Mar 31 18:43:08 GMT 2025 , Edited by admin on Mon Mar 31 18:43:08 GMT 2025
PRIMARY
FDA UNII
944X72NZMV
Created by admin on Mon Mar 31 18:43:08 GMT 2025 , Edited by admin on Mon Mar 31 18:43:08 GMT 2025
PRIMARY
Related Record Type Details
ACTIVE MOIETY