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Targeted therapy! The Capetin Prize winning "Click Chemistry" can be used like this!Targeted therapy! The Nobel Prize winning "Click Chemistry" can be used like this!2025-02-06
59 Results for "
OT
" in MedChemExpress (MCE) Product Catalog:
Products (59)
59 Results for "OT" in MCE Product Catalog:
Cat. No.: HY-W583271
CAS No.: 119700-81-1
Cat. No.: HY-105410
CAS No.: 174858-27-6
Target:
Research Areas:
Neurological Disease Metabolic Disease Inflammation/Immunology
OT-7100 is an orally active analgesic agent. OT-7100 inhibits hyperalgesia possibly by enhancing adenosinergic neurotransmission in the dorsal horn. OT-7100 can be used for the researches of inflammation, neurological and metabolic disease such as diabetes 2].
Cat. No.: HY-W556870
CAS No.: 627085-15-8
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OT-551 is a NF-κB inhibitor with antioxidant and anti-inflammatory effects. OT-551 has the potential for retinal diseases research .
Cat. No.: HY-106429
CAS No.: 627085-11-4
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OT-551 (free base) is a lipophilic, disubstituted hydroxylamine with antioxidant properties. OT-551 can be used as an eye drop and can be converted by intraocular esterases to its active metabolite, Tempol-H (TP-H). OT-551 can be utilized in geographic atrophy and macular degeneration research .
Cat. No.: HY-19495
CAS No.: 870809-51-1
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OT-730 is an innovative selective beta-blocker prodrug designed for research into ocular diseases.
Cat. No.: HY-W415090S
Cat. No.: HY-103652
CAS No.: 2444044-37-3
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OT antagonist 3 analog is an analog of OT antagonist 3.
Cat. No.: HY-103649
CAS No.: 925703-75-9
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Research Areas:
OT antagonist 3 is an oxytocin (OT) antagonist extracted from patent WO2007017752A1.
Cat. No.: HY-103651
CAS No.: 2763705-17-3
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Research Areas:
OT antagonist 1 demethyl derivative is the demethyl derivative of OT antagonist 1. OT antagonist 1 (Compound 4) is a potent, selective Oxytocin antagonist with a Ki of 50 nM.
Cat. No.: HY-15016
CAS No.: 364076-99-3
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(E/Z)-OT-R antagonist 1 is a mixture of E/Z forms of OT-R antagonist 1 (HY-15015). OT-R antagonist 1 is a novel, potent, selective non-peptide OT-R antagonist that inhibits oxytocin-induced intracellular Ca 2+ activation (IC50 = 8 nM) .
Cat. No.: HY-103650
CAS No.: 479080-38-1
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OT antagonist 1 (Compound 4) is a potent, selective Oxytocin antagonist with a Ki of 50 nM.
Cat. No.: HY-RS09893
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OXT Human Pre-designed siRNA Set A contains three designed siRNAs for OXT gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.
Cat. No.: HY-15007
CAS No.: 138382-23-7
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Research Areas:
L 366509 is a spiroindenylpiperidine camphorsulfonamide oxytocin (OT) antagonist. Modifications led to a new series of o-tolylpiperazine (TP) camphorsulfonamides, exhibiting high affinity for OT receptors and selectivity over arginine vasopressin receptors. Notably, compound 7 (L-368,899) showed excellent OT receptor affinity, potency in inhibiting OT-stimulated uterine contractions, good aqueous solubility, and oral bioavailability in multiple species. Compound 7 has entered clinical testing as an oral and intravenous tocolytic agent. Molecular modeling suggests the TP camphorsulfonamide structure mimics the D-AA2-Ile3 dipeptide, crucial in potent OT antagonists .
Cat. No.: HY-153964
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Research Areas:
PF-06478939 is a non-brain-penetrating peptide that is an agonist at oxytocin (OT) receptor and vasopressin receptor with EC50 values of 0.01 nM and 0.078 nM, respectively .
Cat. No.: HY-U00130
CAS No.: 71861-76-2
Synonyms: A-OT-Fu
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Research Areas:
1-Acetyl-3-o-toluyl-5-fluorouracil is a potent antitumor agent and a 5-fluorouracil analog.
Cat. No.: HY-153964A
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Research Areas:
PF-06478939 TFA is a non-brain-penetrating peptide that is an agonist at oxytocin (OT) receptor and vasopressin receptor with EC50 values of 0.01 nM and 0.078 nM, respectively .
Cat. No.: HY-15344A
CAS No.: 1251829-99-8
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Research Areas:
(S,S)-Ketone monoester is a (S,S)-enantiomer of Ketone monoester (HY-15344). Ketone monoester elevates the AcAc and acetone levels, thereby produces sustained ketosis and significantly delays central nervous system oxygen toxicity (CNS-OT) seizures .
Cat. No.: HY-129333
CAS No.: 122211-31-8
Research Areas:
L-364918 is a potent and selective oxytocin and arginine vasopressin antagonist with Ki values of 30, 1300, 2400 nM for OT, AVP-V1, AVP-V2, respectively. L-364918 has the potential for the research of preterm labor and disturbances in water balance .
Synonyms: Lysine vasopressin (Standard); [Lys8]-Vasopressin (Standard)
Category:
Cat. No.: HY-P71766
Purity: ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: OXT; Oxytocin, Prepro- (Neurophysin I); Prev. OT; Neurophysin I; OT-NPI; Oxytocin-Neurophysin I, PreproprOTein; Oxytocin-Neurophysin 1; Oxytocin; OXT-NPI; Oxytocin/Neurophysin I Prepropeptide; Oxytocin, Prepropeptide
Species:
Human
Source:
P. pastoris
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Protocols
Targeted therapy! The Capetin Prize winning "Click Chemistry" can be used like this!Targeted therapy! The Nobel Prize winning "Click Chemistry" can be used like this!A suitable model is crucial in drug screening experiments. Organs can mimic the three-dimensional functional structure of internal organs, have similar spatial organization to corresponding organs, maintain some key characteristics, and reproduce some physiological functions. They are widely used for modeling and personalized drug screening physiological functions.2025-02-06
