Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C64H93N19O20.Lu.H |
| Molecular Weight | 1626.4902 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 4 / 4 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
[H+].[177Lu+3].NC(=O)[C@@H](CCCCNC(=O)CNC(=O)CCC(=O)NCCC1=CN=CN1)NC(=O)[C@@H](CCC([O-])=O)NC(=O)[C@@H](CCCCNC(=O)CNC(=O)CCC(=O)NCCC2=CN=CN2)NC(=O)[C@@H](CC3=CC=C(O)C=C3)NC(=O)CN4CCN(CC([O-])=O)CCN(CC([O-])=O)CCN(CC([O-])=O)CC4
InChI
InChIKey=RRWQZKIZISHPRH-MAEZRVBNSA-K
InChI=1S/C64H97N19O20.Lu/c65-61(100)46(5-1-3-19-68-54(89)34-72-52(87)14-12-50(85)70-21-17-43-32-66-40-74-43)77-63(102)48(11-16-57(92)93)79-62(101)47(6-2-4-20-69-55(90)35-73-53(88)15-13-51(86)71-22-18-44-33-67-41-75-44)78-64(103)49(31-42-7-9-45(84)10-8-42)76-56(91)36-80-23-25-81(37-58(94)95)27-29-83(39-60(98)99)30-28-82(26-24-80)38-59(96)97;/h7-10,32-33,40-41,46-49,84H,1-6,11-31,34-39H2,(H2,65,100)(H,66,74)(H,67,75)(H,68,89)(H,69,90)(H,70,85)(H,71,86)(H,72,87)(H,73,88)(H,76,91)(H,77,102)(H,78,103)(H,79,101)(H,92,93)(H,94,95)(H,96,97)(H,98,99);/q;+3/p-3/t46-,47-,48-,49-;/m1./s1/i;1+2
| Molecular Formula | Lu |
| Molecular Weight | 176.943754987 |
| Charge | 3 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
| Molecular Formula | C64H94N19O20 |
| Molecular Weight | 1449.5465 |
| Charge | -3 |
| Count |
|
| Stereochemistry | ABSOLUTE |
| Additional Stereochemistry | |
| Defined Stereocenters | 4 / 4 |
| E/Z Centers | 5 |
| Optical Activity | UNSPECIFIED |
Approval Year
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 22:25:24 GMT 2025
by
admin
on
Mon Mar 31 22:25:24 GMT 2025
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| Record UNII |
682HJ6Z7F7
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| Record Status |
Validated (UNII)
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| Record Version |
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-
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Code | English |
| Code System | Code | Type | Description | ||
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42628820
Created by
admin on Mon Mar 31 22:25:24 GMT 2025 , Edited by admin on Mon Mar 31 22:25:24 GMT 2025
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PRIMARY | |||
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682HJ6Z7F7
Created by
admin on Mon Mar 31 22:25:24 GMT 2025 , Edited by admin on Mon Mar 31 22:25:24 GMT 2025
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PRIMARY |
| Related Record | Type | Details | ||
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ACTIVE MOIETY |
RESULTS: The highest amount of radioactivity delivered to a subcutaneous colon tumor was achieved by the administration of 5.0 nmol of TF2 and 0.28 nmol of IMP288 in 3 successive cycles, with each IMP288 preceded by a new TF2 injection (72-h interval). PRIT effectively delayed tumor growth and prolonged survival significantly. Higher activity doses, administered in successive cycles, correlated with longer survival: the median survival of untreated mice was 13 d (range, 6-20 d), whereas that of mice treated with 1, 2, or 3 cycles of PRIT was 24 (range, 24-31 d), 45 (range, 38 130 d), and 65 (range, 48 130 d) days, respectively. Toxicity was limited: no significant changes in mean body weight were measured. Minimal changes in leukocyte counts were measured at 2 and 3 wk after injection, with full recovery within 7 wk after treatment. Platelet counts were unaffected. Serum creatinine levels were not increased significantly, thus, there was no indication of acute renal toxicity.
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