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Details

Stereochemistry ABSOLUTE
Molecular Formula C23H30ClN3O2.2H3O4P
Molecular Weight 611.947
Optical Activity UNSPECIFIED
Defined Stereocenters 2 / 2
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of DSP-0390 DIPHOSPHATE

SMILES

OP(O)(O)=O.OP(O)(O)=O.CC1(C)OC2=CC(Cl)=CC=C2[C@@H]3OCC4(CCN(CCN5C=CN=C5)CC4)C[C@@H]13

InChI

InChIKey=SNFDFJIRGSZGNC-NPGCWXMXSA-N
InChI=1S/C23H30ClN3O2.2H3O4P/c1-22(2)19-14-23(5-8-26(9-6-23)11-12-27-10-7-25-16-27)15-28-21(19)18-4-3-17(24)13-20(18)29-22;2*1-5(2,3)4/h3-4,7,10,13,16,19,21H,5-6,8-9,11-12,14-15H2,1-2H3;2*(H3,1,2,3,4)/t19-,21+;;/m1../s1

HIDE SMILES / InChI

Molecular Formula H3O4P
Molecular Weight 97.9952
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula C23H30ClN3O2
Molecular Weight 415.956
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 2 / 2
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

Substance Class Chemical
Created
by admin
on Wed Apr 02 11:49:00 GMT 2025
Edited
by admin
on Wed Apr 02 11:49:00 GMT 2025
Record UNII
HH28W4F6XQ
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
DSP-0390 DIPHOSPHATE
Code English
DSP-0390 DIPHOSPHATE SALT
Preferred Name English
(4'aR,10'bR)-8'-chloro-1-[2-(1H-imidazol-1-yl)ethyl]-5',5'-dimethyl-4'a,10'b-dihydro-2'H,4'H,5'H-spiro[piperidine-4,3'-pyrano[3,2-c][1]benzopyran] diphosphate
Systematic Name English
Spiro[piperidine-4,3?(4?H)-[2H,5H]pyrano[3,2-c][1]benzopyran], 8?-chloro-4?a,10?b-dihydro-1-[2-(1H-imidazol-1-yl)ethyl]-5?,5?-dimethyl-, (4?aR,10?bR)-, phosphate (1:2)
Systematic Name English
Classification Tree Code System Code
FDA ORPHAN DRUG 877322
Created by admin on Wed Apr 02 11:49:00 GMT 2025 , Edited by admin on Wed Apr 02 11:49:00 GMT 2025
Code System Code Type Description
PUBCHEM
166177207
Created by admin on Wed Apr 02 11:49:00 GMT 2025 , Edited by admin on Wed Apr 02 11:49:00 GMT 2025
PRIMARY
CAS
2376766-09-3
Created by admin on Wed Apr 02 11:49:00 GMT 2025 , Edited by admin on Wed Apr 02 11:49:00 GMT 2025
PRIMARY
FDA UNII
HH28W4F6XQ
Created by admin on Wed Apr 02 11:49:00 GMT 2025 , Edited by admin on Wed Apr 02 11:49:00 GMT 2025
PRIMARY
Related Record Type Details
ACTIVE MOIETY