3-Iodo-L-tyrosine - 98%, high purity , CAS No.70-78-0

  • ≥98%
In stock
Item Number
I107816
Grouped product items
SKUSizeAvailabilityPrice Qty
I107816-1g
1g
2
$19.90
I107816-5g
5g
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$59.90
I107816-25g
25g
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$259.90

Tyrosine hydroxylase inhibitor

View related series
Biomodified amino acids (8)

Basic Description

Synonyms(2S)-2-azanyl-3-(3-iodanyl-4-oxidanyl-phenyl)propanoic acid | 3-IODOTYROSINE | IODOTYROSINE | L-Tyrosine-3-iodo | 3-Iodo-L-tyrosine, >=99.0% (HPLC) | CCG-204759 | EN300-6495864 | I0075 | SMR000059143 | FRQ98U4U27 | I-7700 | 4-Hydroxy-3-iodophenylalanine |
Specifications & Purity≥98%
Biochemical and Physiological Mechanisms3-iodotyrosine (3-IY) inhibits tyrosine hydroxylase that catalyzes levodopa (L-DOPA) formation from tyrosine. Iodotyrosine deiodinase enzyme deficiency leads to elevated levels of 3-IY in serum and urine in severe hypothyroidism and goiter. TH (tyrosine 3
Storage TempStore at -20°C,Argon charged
Shipped InIce chest + Ice pads
NoteWherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20°C. Generally, these will be useable for up to one month. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour. Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details.
Product Description

Iodotyrosine coupled with di-iodotyrosine results in the synthesis of 3,5,3′-tri-iodothyronine (T3) or 3,3′,5′-tri-iodothyronine (rT3)
Tyrosine hydroxylase inhibitor.

Associated Targets(Human)

TH Tclin Tyrosine 3-monooxygenase (1 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
TH Tclin Tyrosine 3-hydroxylase (13 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
FPR1 Tchem Formyl peptide receptor 1 (1372 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SLC7A5 Tchem L-type amino acid transporter 1 (388 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
EHMT2 Tchem Histone-lysine N-methyltransferase, H3 lysine-9 specific 3 (93046 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SMN1 Tchem Survival motor neuron protein (34246 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
BLM Tchem Bloom syndrome protein (4248 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
RGS4 Tchem Regulator of G-protein signaling 4 (13867 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

rep Replicase polyprotein 1ab (378 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Txnrd1 Thioredoxin reductase 1, cytoplasmic (45279 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Mechanisms of Action

Mechanism of ActionAction Typetarget IDTarget NameTarget TypeTarget OrganismBinding Site NameReferences

Names and Identifiers

Pubchem Sid504758718
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/504758718
IUPAC Name (2S)-2-amino-3-(4-hydroxy-3-iodophenyl)propanoic acid
INCHI InChI=1S/C9H10INO3/c10-6-3-5(1-2-8(6)12)4-7(11)9(13)14/h1-3,7,12H,4,11H2,(H,13,14)/t7-/m0/s1
InChi Key UQTZMGFTRHFAAM-ZETCQYMHSA-N
Canonical SMILES C1=CC(=C(C=C1CC(C(=O)O)N)I)O
Isomeric SMILES C1=CC(=C(C=C1C[C@@H](C(=O)O)N)I)O
WGK Germany 3
PubChem CID 439744
Molecular Weight 307.09
Beilstein 2941266
Reaxy-Rn 2941266

Certificates(CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

10 results found

Lot NumberCertificate TypeDateItem
C2427165Certificate of AnalysisApr 09, 2024 I107816
C2427164Certificate of AnalysisApr 09, 2024 I107816
C2427166Certificate of AnalysisApr 09, 2024 I107816
L2417152Certificate of AnalysisApr 09, 2024 I107816
C2427163Certificate of AnalysisApr 09, 2024 I107816
H2229643Certificate of AnalysisSep 02, 2022 I107816
G2106156Certificate of AnalysisJul 13, 2021 I107816
K2208117Certificate of AnalysisJul 13, 2021 I107816
G2106158Certificate of AnalysisJul 13, 2021 I107816
G2106157Certificate of AnalysisJul 13, 2021 I107816

Chemical and Physical Properties

SolubilitySoluble in dilute aqeous acid and dilute aqeous base
SensitivityLight sensitive; Air sensitive; Heat sensitive
Specific Rotation[α]-3° (C=2,1mol/L Hcl)
Melt Point(°C)210°C
Molecular Weight307.080 g/mol
XLogP3-1.100
Hydrogen Bond Donor Count3
Hydrogen Bond Acceptor Count4
Rotatable Bond Count3
Exact Mass306.971 Da
Monoisotopic Mass306.971 Da
Topological Polar Surface Area83.600 Ų
Heavy Atom Count14
Formal Charge0
Complexity212.000
Isotope Atom Count0
Defined Atom Stereocenter Count1
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1

Safety and Hazards(GHS)

WGK Germany 3
Reaxy-Rn 2941266
Merck Index 5047

Specifications

Citations of This Product

1. Qinhong Yin, Xiaolan Yang, Lihua Yang, Dezhi Yang, Yaling Yang, Yanqin Zhu.  (2023)  Cu, I-doped carbon dots as simulated nanozymes for the colorimetric detection of morphine in biological samples.  ANALYTICAL BIOCHEMISTRY,  680  (115313).  [PMID:37678583] [10.1016/j.ab.2023.115313]
2. Xiao Li, Yan Xu, Dimei Ouyang, Kefan Ye, Yiwen Chen, Qiulan Li, Qinghai Xia, Xiaomei Wu, Yaling Yang.  (2023)  Copper- and iodine-doped nanozymes with simulated enzyme activity and efficient antifungal activity against Candida albicans.  BIOCHEMICAL ENGINEERING JOURNAL,  191  (108791).  [PMID:] [10.1016/j.bej.2022.108791]
3. Yang Dezhi, Li Qiulan, Zhang Qian, Wang Yijie, Li Hong, Tammina Sai Kumar, Yang Yaling.  (2022)  A multifunctional nanozyme-based enhanced system for tert-butyl hydroquinone assay by surface-enhanced Raman scattering.  MICROCHIMICA ACTA,  189  (1): (1-9).  [PMID:34910256] [10.1007/s00604-021-05135-y]

References

1. Qinhong Yin, Xiaolan Yang, Lihua Yang, Dezhi Yang, Yaling Yang, Yanqin Zhu.  (2023)  Cu, I-doped carbon dots as simulated nanozymes for the colorimetric detection of morphine in biological samples.  ANALYTICAL BIOCHEMISTRY,  680  (115313).  [PMID:37678583] [10.1016/j.ab.2023.115313]
2. Xiao Li, Yan Xu, Dimei Ouyang, Kefan Ye, Yiwen Chen, Qiulan Li, Qinghai Xia, Xiaomei Wu, Yaling Yang.  (2023)  Copper- and iodine-doped nanozymes with simulated enzyme activity and efficient antifungal activity against Candida albicans.  BIOCHEMICAL ENGINEERING JOURNAL,  191  (108791).  [PMID:] [10.1016/j.bej.2022.108791]
3. Yang Dezhi, Li Qiulan, Zhang Qian, Wang Yijie, Li Hong, Tammina Sai Kumar, Yang Yaling.  (2022)  A multifunctional nanozyme-based enhanced system for tert-butyl hydroquinone assay by surface-enhanced Raman scattering.  MICROCHIMICA ACTA,  189  (1): (1-9).  [PMID:34910256] [10.1007/s00604-021-05135-y]

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