Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C9H10INO2 |
| Molecular Weight | 291.0857 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 1 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
N[C@@H](CC1=CC=C(I)C=C1)C(O)=O
InChI
InChIKey=PZNQZSRPDOEBMS-QMMMGPOBSA-N
InChI=1S/C9H10INO2/c10-7-3-1-6(2-4-7)5-8(11)9(12)13/h1-4,8H,5,11H2,(H,12,13)/t8-/m0/s1
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Application of the Suzuki-Miyaura cross-coupling to increase antimicrobial potency generates promising novel antibacterials. | 2007 Apr 15 |
|
| Halogen-substituted phenylalanines as enantioselective selectors for enantioselective discrimination of amino acids: effect of halogen. | 2008 May |
|
| Efficacy of systemic radionuclide therapy with p-131I-iodo-L-phenylalanine combined with external beam photon irradiation in treating malignant gliomas. | 2009 Dec |
|
| Expanded chemical diversity sampling through whole protein evolution. | 2009 Jul |
|
| Site-specific incorporation of 4-iodo-L-phenylalanine through opal suppression. | 2010 Aug |
|
| Genetic incorporation of unnatural amino acids into proteins in Mycobacterium tuberculosis. | 2010 Feb 22 |
Patents
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| Code System | Code | Type | Description | ||
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DB03660
Created by
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134497
Created by
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J882Z73MPL
Created by
admin on Sat Dec 16 02:05:38 GMT 2023 , Edited by admin on Sat Dec 16 02:05:38 GMT 2023
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145892
Created by
admin on Sat Dec 16 02:05:38 GMT 2023 , Edited by admin on Sat Dec 16 02:05:38 GMT 2023
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24250-85-9
Created by
admin on Sat Dec 16 02:05:38 GMT 2023 , Edited by admin on Sat Dec 16 02:05:38 GMT 2023
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C049181
Created by
admin on Sat Dec 16 02:05:38 GMT 2023 , Edited by admin on Sat Dec 16 02:05:38 GMT 2023
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300000026359
Created by
admin on Sat Dec 16 02:05:38 GMT 2023 , Edited by admin on Sat Dec 16 02:05:38 GMT 2023
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44964
Created by
admin on Sat Dec 16 02:05:38 GMT 2023 , Edited by admin on Sat Dec 16 02:05:38 GMT 2023
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PRIMARY |
SUBSTANCE RECORD
