Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C37H41N5O9S.2K.Pd |
| Molecular Weight | 916.43 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 4 / 4 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
[K+].[K+].[Pd++].CC[C@@H]1[C@@H](C)C2=NC1=CC3=C(C)C(C(=O)NCCS([O-])(=O)=O)=C([N-]3)C(CC(=O)OC)=C4N=C(C=C5[N-]C(=C2)C(C(C)=O)=C5C)[C@@H](C)[C@@H]4CCC([O-])=O
InChI
InChIKey=AOSMIFSJINLACN-NAEAMVODSA-J
InChI=1S/C37H45N5O9S.2K.Pd/c1-8-22-17(2)25-16-30-33(21(6)43)19(4)27(40-30)14-26-18(3)23(9-10-31(44)45)35(41-26)24(13-32(46)51-7)36-34(37(47)38-11-12-52(48,49)50)20(5)28(42-36)15-29(22)39-25;;;/h14-18,22-23H,8-13H2,1-7H3,(H5,38,39,40,41,42,43,44,45,47,48,49,50);;;/q;2*+1;+2/p-4/t17-,18+,22-,23+;;;/m1.../s1
| Molecular Formula | K |
| Molecular Weight | 39.0983 |
| Charge | 1 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
| Molecular Formula | Pd |
| Molecular Weight | 106.42 |
| Charge | 2 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
| Molecular Formula | C37H43N5O9S |
| Molecular Weight | 733.83 |
| Charge | -2 |
| Count |
|
| Stereochemistry | ABSOLUTE |
| Additional Stereochemistry | No |
| Defined Stereocenters | 4 / 4 |
| E/Z Centers | 0 |
| Optical Activity | UNSPECIFIED |
Padeliporfin is a vascular-acting photosensitizer consisting of a water-soluble, palladium-substituted bacteriochlorophyll derivative with antineoplastic activity. After administration, the drug is activated locally when the tumor bed is exposed to low-power laser light; reactive oxygen species (ROS) are formed upon activation and ROS-mediated necrosis may occur at the site of interaction between the photosensitizer, light and oxygen. Padeliporfin is approved in Europe for the treatment of adult patients with previously untreated, unilateral, low-risk, adenocarcinoma of the prostate and is marketed under tradename TOOKAD.
Approval Year
| Substance Class |
Chemical
Created
by
admin
on
Edited
Wed Apr 02 01:00:31 GMT 2025
by
admin
on
Wed Apr 02 01:00:31 GMT 2025
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| Record UNII |
JQ72VD4XUL
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| Record Status |
Validated (UNII)
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| Record Version |
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HI-09
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m12050
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100000166789
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129629432
Created by
admin on Wed Apr 02 01:00:31 GMT 2025 , Edited by admin on Wed Apr 02 01:00:31 GMT 2025
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C175732
Created by
admin on Wed Apr 02 01:00:31 GMT 2025 , Edited by admin on Wed Apr 02 01:00:31 GMT 2025
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JQ72VD4XUL
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698393-30-5
Created by
admin on Wed Apr 02 01:00:31 GMT 2025 , Edited by admin on Wed Apr 02 01:00:31 GMT 2025
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PRIMARY |
| Related Record | Type | Details | ||
|---|---|---|---|---|
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PARENT -> SALT/SOLVATE |
| Related Record | Type | Details | ||
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ACTIVE MOIETY |