Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C17H23N5O4 |
| Molecular Weight | 361.3956 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 1 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
NC(=N)C1=CC=C(C=C1)N2C[C@@H](CN3CCN(CC(O)=O)CC3)OC2=O
InChI
InChIKey=BXTGCIBGRDGLNI-CQSZACIVSA-N
InChI=1S/C17H23N5O4/c18-16(19)12-1-3-13(4-2-12)22-10-14(26-17(22)25)9-20-5-7-21(8-6-20)11-15(23)24/h1-4,14H,5-11H2,(H3,18,19)(H,23,24)/t14-/m1/s1
| Molecular Formula | C17H23N5O4 |
| Molecular Weight | 361.3956 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ABSOLUTE |
| Additional Stereochemistry | No |
| Defined Stereocenters | 1 / 1 |
| E/Z Centers | 0 |
| Optical Activity | UNSPECIFIED |
Gantofiban (or EMD 122 347) is an oral double prodrug of the drug, EMD 132338 and is GPIIb/IIIa antagonist. The drug participated in phase II clinical trials in Japan in patients with thrombosis. However, in May 2004, Yamanouchi, the developing company, announced that the study was discontinued. Besides gantofiban was involved in phase II trials, like a treatment option in patients with the acute coronary syndrome. However, further information is not available.
Originator
Approval Year
| Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 19:50:15 UTC 2023
by
admin
on
Sat Dec 16 19:50:15 UTC 2023
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| Record UNII |
9Y2SN3W6A3
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| Record Status |
Validated (UNII)
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| Record Version |
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-
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9950809
Created by
admin on Sat Dec 16 19:50:15 UTC 2023 , Edited by admin on Sat Dec 16 19:50:15 UTC 2023
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9Y2SN3W6A3
Created by
admin on Sat Dec 16 19:50:15 UTC 2023 , Edited by admin on Sat Dec 16 19:50:15 UTC 2023
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167364-01-4
Created by
admin on Sat Dec 16 19:50:15 UTC 2023 , Edited by admin on Sat Dec 16 19:50:15 UTC 2023
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PRIMARY |
| Related Record | Type | Details | ||
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PRODRUG -> METABOLITE ACTIVE |
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| Related Record | Type | Details | ||
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ACTIVE MOIETY |
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