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Results for "

9(z),12(z),15(z),18(z),21(z) tetracosapentaenoic acid

" in TargetMol Product Catalog
  • Inhibitors & Agonists
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9(Z),12(Z),15(Z),18(Z),21(Z)-Tetracosapentaenoic Acid
T3827868378-48-3
9(Z),12(Z),15(Z),18(Z),21(Z)-Tetracosapentaenoic acid is an ω-3 very long-chain polyunsaturated fatty acid. It has been used to study the desaturation and elongation of ω-3 polyunsaturated fatty acids. It is elongated to form C26:5 or acted on by δ6 desaturase to form C24:6. 9(Z),12(Z),15(Z),18(Z),21(Z)-Tetracosapentaenoic acid is found at low levels in mouse brain and spleen and levels decrease in the brain and spleen of old and exceptionally old mice.
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Z-VAD-FMK
Z-VAD(OH)-FMK,Caspase Inhibitor VI,Z-VAD
T7020161401-82-7
Z-VAD-FMK (Caspase Inhibitor VI) is a broad-spectrum inhibitor of caspases.Z-VAD-FMK binds to activated caspases and inhibits apoptosis.Z-VAD-FMK does not inhibit UCHL1 activity, even at concentrations up to 440 μM.
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Z-DEVD-FMK
Caspase-3 Inhibitor
T6005210344-95-9
Z-DEVD-FMK (Caspase-3 Inhibitor) is a selective, irreversible Caspase-3 inhibitor, and also exhibits effective inhibition activity on caspase-6, caspase-7, caspase-8, and caspase-10.
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Z-VAD(OMe)-FMK
Z-VAD-FMK,Z-Val-Ala-Asp(OMe)-FMK
T6013187389-52-2
Z-VAD(OMe)-FMK is a pan-caspase inhibitor with irreversible properties; Z-VAD(OMe)-FMK is also an inhibitor of ubiquitin C terminal hydrolase L1 (UCHL1), which is irreversibly modified by targeting the UCHL1 active site.
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(Z)-Metanicotine 2HCl
(Z)-Metanicotine 2HCl(1129-68-6 Free base)
T77676 In house
(Z)-Metanicotine 2HCl has analgesic activity and is used in the treatment of central system disorders.
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Bis(2-methoxy-5-((Z)-3,4,5-trimethoxystyryl)phenyl) hydrogen phosphate
T67906735261-22-0In house
Phenol, 2-methoxy-5-[(1Z)-2-(3,4,5-trimethoxyphenyl)ethenyl]-, 1,1'-(hydrogen phosphate) is a chemical compound that is a phosphate derivative of the statin class.
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6-8weeks
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(Z)-Tenilapine
T8364782650-82-6In house
(Z)-Tenilapine is trans-Tenilapine, cis-Tenilapine has sedative activity.
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(Z)-2-fluoro-1,3-bis(4-methoxyphenyl)prop-2-en-1-one
SJD00639
T85319126912-62-7In house
(Z)-2-fluoro-1,3-bis(4-methoxyphenyl)prop-2-en-1-one is a screening compound and can be used in new drug development related research.
    Inquiry
    Z-Lys-OH
    T658682212-75-1
    Z-Lys-OH is a competitive inhibitor of papain, a lysine derivative.
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    7-10 days
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    (Z)-4-Amino-4-oxobut-2-enoic acid
    Maleamic acid,Acrylic acid
    T4905557-24-4
    (Z)-4-Amino-4-oxobut-2-enoic acid (Maleamic acid) is a valuable compound for research applications.
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    (E/Z)-Squalene
    (E Z)-Super Squalene,(E Z)-AddaVax
    T756367683-64-9
    (E Z)-Squalene ((E Z)-AddaVax) regulates intracellular reactive oxidant species (ROS) production, induces apoptosis and necrosis in a concentration- and time-dependent manner, accumulates in the liver, and lowers hepatic cholesterol and triglycerides.
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    15-hydroxypentadecanoic acid
    T841834617-33-8
    15-hydroxypentadecanoic acid is a fatty acid found in soybean oil and rapeseed oil that has anti-inflammatory, antibacterial, and antioxidant activities.
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    (E/Z)-Polydatin
    Polydatin,(E Z)-Piceid
    T293865914-17-2
    (E Z)-Polydatin (Polydatin), is a natural precursor and glycoside form of resveratrol with a monocrystalline structure. While it is isolated from the bark of Picea sitchensis or Polygonum cuspidatum, Polydatin may be detected in grape, peanut, hop cones, red wines, hop pellets, cocoa-containing products, chocolate products and many daily diets. Polydatin possesses anti-inflammatory, immunoregulatory, anti-oxidative and anti-tumor activities. It is shown to mediate a cytotoxic action on colorectal cancer cells by inducing cell arrest and apoptosis.
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    (Z)-1-(1-ethoxyethoxy)hex-3-ene
    (3Z)-1-(1-Ethoxyethoxy)-3-hexene
    T8406628069-74-1
    (Z)-1-(1-ethoxyethoxy)hex-3-ene ((3Z)-1-(1-Ethoxyethoxy)-3-hexene) can be used to synthesize compounds with special effects.
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    (Z)-3-Hexenyl isovalerate
    (3Z)-3-Hexen-1-yl 3-methylbutanoate
    T8408735154-45-1
    (Z)-3-Hexenyl isovalerate ((3Z)-3-Hexen-1-yl 3-methylbutanoate) is a RIFM fragrance and one of the aroma components in Xinyang Maojian.
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    Z-Asp(OBzl)-OH
    N-Cbz-L-Aspartic acid 4-benzyl ester,Cbz-Asp(OBzl)-OH
    T643263479-47-8
    Z-Asp(OBzl)-OH (N-Cbz-L-Aspartic acid 4-benzyl ester) is an aspartic acid derivative.
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    4-(9H-fluoren-9-ylmethoxycarbonylamino)-piperidine-1,4-dicarboxylic acid mono-tert-butyl ester
    T64322183673-66-7
    4-(9H-fluoren-9-ylmethoxycarbonylamino)-piperidine-1,4-dicarboxylic acid mono-tert-butyl ester is a substituted piperidine derivative widely used in organic synthesis as a linker to form peptide and peptidomimetic molecules, and is widely used in peptide synthesis and peptide mimicry, as well as in the synthesis of pharmaceuticals, biopolymers and other organic molecules.
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    Z-Glycine
    Carbobenzoxyglycine,N-Carbobenzoxyglycine
    T336041138-80-3
    Z-Glycine (Carbobenzoxyglycine) is a drug-lipid conjugates designed to promote brain penetration based on its lipophilicity and resemblance to lipids in biological membranes[1].
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    Geranylacetone(Z/E)
    Dihydropseudoionone
    T8368689-67-8
    Geranylacetone(Z/E) (Dihydropseudoionone) is a naturally occurring compound found in the essential oils of many plants, including rosemary, lavender and jasmine. It has antioxidant, anti-inflammatory and anti-microbial properties.
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    (Z)-Butylidenephthalide
    (Z)-3-Butylidenephthalide
    TN232672917-31-8
    (Z)-Butylidenephthalide ((Z)-3-Butylidenephthalide) has antitumor and hypoglycemic effects, and can effectively inhibit the tumor growth of glioma and inhibit R-glucosidase activity.
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    Z-Arg(Z)2-OH
    NSC120011,NSC-120011,NSC 120011,Tris(benzyloxycarbonyl)arginine
    T2049014611-34-8
    Z-Arg(Z)2-OH can be used in the assay to screen proteolytic activities in mite homogenates.
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    4-6 weeks
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    (Z)-3-Hexenyl tiglate
    (3Z)-Hex-3-en-1-yl (2E)-2-methylbut-2-enoate
    T8407867883-79-8
    (Z)-3-Hexenyl tiglate ((3Z)-Hex-3-en-1-yl (2E)-2-methylbut-2-enoate) is a RIFM fragrance that can be used in paints, coatings, inks, resins and other fields.
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    3-(3,6-dichloro-9H-carbazol-9-yl)propanoic acid
    T50021300816-42-6
    3-(3,6-dichloro-9H-carbazol-9-yl)propanoic acid (DCPPA) is an ASIC3 inhibitor that effectively blocks ASIC3-mediated pain and inflammation. It has been shown to have potential applications in the treatment of other diseases such as stroke, epilepsy and cancer.
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    β-Amyloid 15-21 acetate
    Beta-Amyloid (15-21) acetate
    TP1214L
    β-Amyloid 15-21 acetate (Beta-Amyloid (15-21) acetate) is a fragment of Amyloid-β peptide, maybe used in the research of neurological disease. This fragment is involved in beta sheet formation.
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    GW406108X(Z/E)
    T9207L265098-01-9
    GW406108X(Z/E) is a mixture of different configurations of GW406108X, which is an inhibitor of Kinesin-12 and ULK1 .
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    (Z)-8-Dodecenyl acetate
    Orfralure
    T2050828079-04-1
    (Z)-8-Dodecenyl acetate (Orfralure) is a pear psyllid sex pheromone, which can be used to study pear psyllid control.
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    9-Oxononanoic Acid
    9-ONA
    T368312553-17-5
    9-Oxononanoic Acid is an oxidized fatty acid, formed by the autoxidation of linoleic acid, which enhances phospholipase A2 (PLA2) activity and increases the production of thromboxane B2 in isolated human plasma.9-Oxononanoic Acid reduces hepatic neofatty acid synthesis and enhances the activity of rat hepatic carnitine palmitoyltransferase, a marker of β-oxidation. Activity.
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    (Z)-Nexinhib20
    T777661162656-24-7
    (Z)-Nexinhib20 is a biochemical reagent that can be used in biological experiments.
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    (Z)-MDL 105519
    T16032L179105-67-0
    (Z)-MDL 105519 is an inactive isomer of MDL105519.
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    (Z)-Semaxinib
    SU5416
    T2496194413-58-6
    (Z)-Semaxinib (SU5416) is a potent and selective VEGFR(Flk-1/KDR) inhibitor (IC50: 1.23 μM), 20-fold more selective for VEGFR over PDGFRβ, no inhibition for FGFR, InsR, and EGFR. (Z)-Semaxinib is a quinolone derivative with potential antineoplastic activity.
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    (Z)-SU4312
    T567690828-16-3
    (Z)-SU4312 is a inhibitor of MAO-B and NOS(IC50 value of 0.2 μM, 19.0μM,respectively).
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    (Z)-Dodec-5-en-1-ol
    (Z)-Dodec-5-enol
    T8409340642-38-4
    (Z)-Dodec-5-en-1-ol ((Z)-Dodec-5-enol) is a pheromone of pine caterpillars and yellow flower moths.
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    Z-Gly-Gly-Arg-AMC TFA (66216-78-2 free base)
    Z-Gly-Gly-Arg-AMC TFA
    T855666216-79-3
    Z-Gly-Gly-Arg-AMC TFA (66216-78-2 free base) is a thrombin-specific fluorogenic substrate used to assess thrombin generation in platelet-rich plasma (PRP) and platelet-poor plasma (PPP).
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    methyl (Z)-4-(2-amino-5-(4-((dimethylamino)methyl)thiophen-2-yl)pyridin-3-yl)-2-((5,5,5-trifluoropent-3-en-2-yl)oxy)benzoate
    T600591364268-07-4In house
    methyl(Z)-4-(2-amino-5-(4-((dimethylamino)methyl)thiophen-2-yl)pyridin-3-yl)-2-((5,5,5-trifluoropent-3-en-2-yl)oxy)benzoate is a useful compound for the synthesis of a variety of organic compounds.
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    6-8 weeks
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    (E/Z)-Sivopixant
    (E Z)-S-600918
    T96531640808-39-4In house
    (E Z)-Sivopixant ((E Z)-S-600918) is a potent P2X3 receptor antagonist with an IC50 of 4 nM, suitable for respiratory diseases research.
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    Z-FY-CHO
    T41236167498-29-5In house
    Z-FY-CHO (Z-Phe-Tyr-CHO) is a specific and potent cathepsin L (CTSL) inhibitor [1][2].
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    10-14 weeks
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    Falintolol, (Z)-
    T11262106401-52-9In house
    Falintolol, (Z)-, is a novel β-adrenergic antagonist compound distinguished by the inclusion of an oxime moiety.
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    6-8 weeks
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    (Z)-FeCP-oxindole
    T235541137967-28-2In house
    (Z)-FeCP-oxindole is a selective inhibitor of VEGFR2 with an IC50 of 200 nM for humans and demonstrates anticancer activity.
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    6-8 weeks
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    (Z)-Guggulsterone
    T1728039025-23-5
    (Z)-Guggulsterone inhibits the growth of human prostate cancer cells by causing apoptosis. Z-guggulsterone inhibits angiogenesis by suppressing the VEGF–VEGF-R2–Akt signaling axis.
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    (E/Z)-Necrosulfonamide
    T7129432531-71-0
    (E/Z)-Necrosulfonamide is a novel inhibitor of MLKL.
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    Nikkomycin Z
    Nikkomycin Z from Streptomyces tendae
    T881459456-70-1
    Nikkomycin Z (Nikkomycin Z from Streptomyces tendae) is a competitive chitin synthase inhibitor.It inhibitor of the growth of filamentous fungi, insects, acarids and yeasts.
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    10-14 weeks
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    Z-YVAD-FMK
    TP1466210344-97-1
    AA-Z-YVAD-FMK is a Irreversible caspase-1 inhibitor,with anti-inflammatory and anti-tumor activities.
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    (E/Z)-4-Hydroxytamoxifen
    Afimoxifene,4-Hydroxytamoxifen
    T674368392-35-8
    (E Z)-4-Hydroxytamoxifen (Afimoxifene) is a novel estrogen inhibitor, commonly used in research for various estrogen-dependent conditions, including cyclic mastalgia and gynecomastia.
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    Z-VEID-FMK
    T23555
    When compared to other caspase inhibitors, Z-DRHD-FMK inhibited caspase 6 activity more effectively than the general caspase inhibitor of Z-Val-Ala-Asp (OMe)-fluoromethy ketone (Z-VAD-FMK) or the caspase 6 inhibitor Z-Val-Glu(Ome)-Ile-Asp(OMe)-fluorometh
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    Endoxifen Z-isomer hydrochloride
    Endoxifen HCl
    T68271032008-74-4
    Endoxifen Z-isomer hydrochloride (Endoxifen HCl) is the active metabolite of Tamoxifen, which is an effective and selective estrogen receptor antagonist.
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    7-10 days
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    Z-IETD-FMK
    Z-IE(OMe)TD(OMe)-FMK,Caspase-8 Inhibitor
    T7019210344-98-2
    Z-IETD-FMK (Z-IE(OMe)TD(OMe)-FMK) is a cell-permeable, selective inhibitor of caspase 8.
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    (E/Z)-BCI
    NSC 150117
    T1113915982-84-0
    (E Z)-BCI (NSC-150117), a dual-specificity phosphatase 6 (DUSP6) inhibitor with anti-inflammatory properties, reduces LPS-induced inflammatory mediators and ROS production in macrophage cells by activating the Nrf2 signaling axis and inhibiting the NF-κB pathway.
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    Anthracene-9-carboxylic acid
    T8632723-62-6
    Anthracene-9-carboxylic acid is an inhibitor of chloride transport with a moderate to strong inhibitory action on PKA activated cardiac IcI.
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