Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C24H26FN3O2 |
| Molecular Weight | 407.4805 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC1=CN2C(=O)C(CCN3CCC(CC3)C(=O)C4=CC=C(F)C=C4)=C(C)N=C2C=C1
InChI
InChIKey=AXQRPYKSPHUOGZ-UHFFFAOYSA-N
InChI=1S/C24H26FN3O2/c1-16-3-8-22-26-17(2)21(24(30)28(22)15-16)11-14-27-12-9-19(10-13-27)23(29)18-4-6-20(25)7-5-18/h3-8,15,19H,9-14H2,1-2H3
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Metrenperone enhances collagen turnover and remodeling in the early stages of healing of tendon injury in rabbit. | 2010-12 |
|
| Effects of a serotonin S2-receptor blocker on healing of acute and chronic tendon injuries. | 2009-10-22 |
|
| Cardiovascular response to intravenous administration of 5-hydroxytryptamine after type-2 receptor blockade, by metrenperone, in healthy calves. | 1999-01 |
|
| Economic, clinical and functional consequences of a treatment using metrenperone during an outbreak of shipping fever in cattle. | 1993-03-06 |
| Name | Type | Language | ||
|---|---|---|---|---|
|
Official Name | English | ||
|
Preferred Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Code | English | ||
|
Code | English | ||
|
Common Name | English |
| Classification Tree | Code System | Code | ||
|---|---|---|---|---|
|
NCI_THESAURUS |
C66885
Created by
admin on Mon Mar 31 18:30:03 GMT 2025 , Edited by admin on Mon Mar 31 18:30:03 GMT 2025
|
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
81043-56-3
Created by
admin on Mon Mar 31 18:30:03 GMT 2025 , Edited by admin on Mon Mar 31 18:30:03 GMT 2025
|
PRIMARY | |||
|
100000080926
Created by
admin on Mon Mar 31 18:30:03 GMT 2025 , Edited by admin on Mon Mar 31 18:30:03 GMT 2025
|
PRIMARY | |||
|
72005
Created by
admin on Mon Mar 31 18:30:03 GMT 2025 , Edited by admin on Mon Mar 31 18:30:03 GMT 2025
|
PRIMARY | |||
|
BB-21
Created by
admin on Mon Mar 31 18:30:03 GMT 2025 , Edited by admin on Mon Mar 31 18:30:03 GMT 2025
|
PRIMARY | |||
|
W1O4FV809G
Created by
admin on Mon Mar 31 18:30:03 GMT 2025 , Edited by admin on Mon Mar 31 18:30:03 GMT 2025
|
PRIMARY | |||
|
279-678-7
Created by
admin on Mon Mar 31 18:30:03 GMT 2025 , Edited by admin on Mon Mar 31 18:30:03 GMT 2025
|
PRIMARY | |||
|
DTXSID20230867
Created by
admin on Mon Mar 31 18:30:03 GMT 2025 , Edited by admin on Mon Mar 31 18:30:03 GMT 2025
|
PRIMARY | |||
|
SUB08917MIG
Created by
admin on Mon Mar 31 18:30:03 GMT 2025 , Edited by admin on Mon Mar 31 18:30:03 GMT 2025
|
PRIMARY | |||
|
C80774
Created by
admin on Mon Mar 31 18:30:03 GMT 2025 , Edited by admin on Mon Mar 31 18:30:03 GMT 2025
|
PRIMARY | |||
|
CHEMBL2104852
Created by
admin on Mon Mar 31 18:30:03 GMT 2025 , Edited by admin on Mon Mar 31 18:30:03 GMT 2025
|
PRIMARY | |||
|
6033
Created by
admin on Mon Mar 31 18:30:03 GMT 2025 , Edited by admin on Mon Mar 31 18:30:03 GMT 2025
|
PRIMARY | |||
|
C046881
Created by
admin on Mon Mar 31 18:30:03 GMT 2025 , Edited by admin on Mon Mar 31 18:30:03 GMT 2025
|
PRIMARY |
ACTIVE MOIETY