Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C86H134N20O19 |
| Molecular Weight | 1752.1101 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 15 / 15 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
[H][C@](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)[C@@]([H])(NC(=O)[C@@H]2CCCN2C(=O)[C@@H](NC(=O)[C@H](CC3=CC=CC=C3)[N+](C)(C)C)C(C)C)[C@@H](C)CC)([C@@H](C)O)C(=O)N[C@@H](CC4=CC=C(O)C=C4)C(=O)NCC(=O)N[C@@H](CCC([O-])=O)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@H](CCCNC(N)=N)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCCCN)C(N)=O
InChI
InChIKey=DUQRILZXKXSRIY-RUBJUKRASA-N
InChI=1S/C86H134N20O19/c1-13-51(8)71(103-81(121)65-30-23-41-105(65)85(125)70(50(6)7)102-82(122)66(106(10,11)12)46-54-26-18-15-19-27-54)83(123)101-64(44-53-24-16-14-17-25-53)80(120)104-72(52(9)107)84(124)100-63(45-55-31-33-56(108)34-32-55)74(114)93-47-68(110)94-59(36-38-69(111)112)76(116)99-62(43-49(4)5)79(119)97-60(35-37-67(88)109)77(117)96-58(29-22-40-92-86(90)91)75(115)98-61(42-48(2)3)78(118)95-57(73(89)113)28-20-21-39-87/h14-19,24-27,31-34,48-52,57-66,70-72,107H,13,20-23,28-30,35-47,87H2,1-12H3,(H21-,88,89,90,91,92,93,94,95,96,97,98,99,100,101,102,103,104,108,109,110,111,112,113,114,115,116,117,118,119,120,121,122,123,124)/t51-,52+,57-,58+,59-,60-,61-,62-,63-,64-,65-,66-,70-,71-,72-/m0/s1
| Molecular Formula | C86H134N20O19 |
| Molecular Weight | 1752.1101 |
| Charge | 0 |
| Count |
|
| Stereochemistry | EPIMERIC |
| Additional Stereochemistry | No |
| Defined Stereocenters | 15 / 15 |
| E/Z Centers | 0 |
| Optical Activity | UNSPECIFIED |
Atilmotin (also known as BAX-ACC-1638), a motilin receptor agonist, is short acting, with t1/2 less than 10 min. It was shown that at doses of 6, 30 or 60 mg intravenously, it affected esophageal, lower esophageal sphincter (LES), and gastric motility. LES and gastric pressures were increased, whereas there was disruption of esophageal peristalsis characterized by lower amplitude and failed contractions. The drug can have the clinical implementation for stomach motility disorders but is needed further study.
Approval Year
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/16371080
i.v. atilmotin, 6, 30, 60 microg or vehicle (placebo) given 2 min after standardized breakfast, lunch and dinner
Route of Administration:
Intravenous
| Substance Class |
Chemical
Created
by
admin
on
Edited
Wed Apr 02 07:37:08 GMT 2025
by
admin
on
Wed Apr 02 07:37:08 GMT 2025
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| Record UNII |
4WQQ18VL49
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| Record Status |
FAILED
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| Record Version |
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-
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Official Name | English | ||
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Preferred Name | English | ||
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Systematic Name | English | ||
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Common Name | English | ||
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Common Name | English | ||
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Common Name | English | ||
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Code | English | ||
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Code | English |
| Classification Tree | Code System | Code | ||
|---|---|---|---|---|
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NCI_THESAURUS |
C548
Created by
admin on Wed Apr 02 07:37:08 GMT 2025 , Edited by admin on Wed Apr 02 07:37:08 GMT 2025
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| Code System | Code | Type | Description | ||
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C508748
Created by
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PRIMARY | |||
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533927-56-9
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4WQQ18VL49
Created by
admin on Wed Apr 02 07:37:08 GMT 2025 , Edited by admin on Wed Apr 02 07:37:08 GMT 2025
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C77604
Created by
admin on Wed Apr 02 07:37:08 GMT 2025 , Edited by admin on Wed Apr 02 07:37:08 GMT 2025
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917220-41-8
Created by
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ALTERNATIVE | |||
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300000034168
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DTXSID40201559
Created by
admin on Wed Apr 02 07:37:08 GMT 2025 , Edited by admin on Wed Apr 02 07:37:08 GMT 2025
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PRIMARY | |||
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73348450
Created by
admin on Wed Apr 02 07:37:08 GMT 2025 , Edited by admin on Wed Apr 02 07:37:08 GMT 2025
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8565
Created by
admin on Wed Apr 02 07:37:08 GMT 2025 , Edited by admin on Wed Apr 02 07:37:08 GMT 2025
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QQ-40
Created by
admin on Wed Apr 02 07:37:08 GMT 2025 , Edited by admin on Wed Apr 02 07:37:08 GMT 2025
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PRIMARY | |||
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CHEMBL2369989
Created by
admin on Wed Apr 02 07:37:08 GMT 2025 , Edited by admin on Wed Apr 02 07:37:08 GMT 2025
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PRIMARY |
| Related Record | Type | Details | ||
|---|---|---|---|---|
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TARGET -> AGONIST |
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| Related Record | Type | Details | ||
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ACTIVE MOIETY |
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