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Endocrinologie/Hormones

Endocrinologie/Hormones

Les inhibiteurs en endocrinologie/hormonaux sont des composés qui bloquent l'action des hormones ou interfèrent avec les voies de signalisation hormonales. Ces inhibiteurs sont essentiels pour étudier la régulation des systèmes endocriniens et pour développer des traitements pour les maladies liées aux hormones, telles que le diabète, les troubles de la thyroïde et les cancers hormonodépendants. En modulant l'activité hormonale, ces inhibiteurs peuvent aider à élucider les interactions complexes au sein du système endocrinien. Chez CymitQuimica, nous offrons une large gamme d'inhibiteurs de haute qualité en endocrinologie/hormonaux pour soutenir vos recherches en endocrinologie, pharmacologie et sciences médicales.

Sous-catégories appartenant à la catégorie "Endocrinologie/Hormones"

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3371 produits trouvés pour "Endocrinologie/Hormones"

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  • AKR1C3-IN-5


    AKR1C3-IN-5 inhibits AKR1C3, key in prostate/breast cancers, with MCF-7 cell IC50 of 9.6 μM.
    Formule :C34H44N2O7
    Couleur et forme :Solid
    Masse moléculaire :592.72

    Ref: TM-T64193

    25mg
    1.369,00€
    50mg
    1.783,00€
    100mg
    2.250,00€
  • Erα-IN-1


    Erα-IN-1 (compound 3c) is an inhibitor of the estrogen receptor α (ERα), effectively blocking ERα activity in MCF7/ERE-LUC cells.
    Formule :C16H11FN2
    Couleur et forme :Solid
    Masse moléculaire :250.27

    Ref: TM-T201461

    10mg
    À demander
    50mg
    À demander
  • Emd 52297

    CAS :
    Emd 52297 is an inhibitor of renin.
    Formule :C39H59N11O7
    Degré de pureté :98%
    Couleur et forme :Solid
    Masse moléculaire :793.96

    Ref: TM-T25369

    25mg
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    50mg
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    100mg
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  • BMS-986034

    CAS :
    BMS-986034 is a GPR119 agonist.
    Formule :C24H24Cl2N6O4
    Couleur et forme :Solid
    Masse moléculaire :531.39

    Ref: TM-T70550

    25mg
    2.043,00€
    50mg
    2.682,00€
    100mg
    3.600,00€
  • RJG-2051

    CAS :
    RJG-2051 is a selective covalent inhibitor of aldo-keto reductase family 1 member C3 (AKR1C3), with an IC50 value of 13 nM. It interferes with the metabolism of substrates such as androgens, estrogens, and prostaglandins through AKR1C3. RJG-2051 holds potential for cancer research.
    Formule :C26H31N5O4S
    Couleur et forme :Solid
    Masse moléculaire :509.62

    Ref: TM-T206799

    10mg
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    50mg
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  • Mu opioid receptor antagonist 4


    Compound 31: Potent, selective MOR antagonist; crosses blood-brain barrier; Ki & EC50: 0.38 nM; useful for OUD research.
    Formule :C25H28N2O4S
    Couleur et forme :Solid
    Masse moléculaire :452.57

    Ref: TM-T62768

    25mg
    1.444,00€
    50mg
    1.882,00€
    100mg
    2.375,00€
  • MTI013


    MTI013 is a selective inhibitor of SARS-CoV-2 nsp14 Mtase (IC50: 2.98 µM) and an antiviral agent (IC50: 10.33 µM in HCoV-229E infected Huh7 cells). Additionally, MTI013 demonstrates synergistic antiviral effects when used in conjunction with the RdRp inhibitor SHEN26.
    Formule :C24H26N6O4S
    Couleur et forme :Solid
    Masse moléculaire :494.57

    Ref: TM-T201844

    10mg
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    50mg
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  • Estrogen receptor antagonist 6

    CAS :
    Estrogen receptor antagonist 6 is a potent blocker of estrogen signaling, regulating various biological effects. (Compound 166)
    Formule :C25H31F3N2O3
    Couleur et forme :Solid
    Masse moléculaire :464.52

    Ref: TM-T62953

    25mg
    1.927,00€
    50mg
    2.507,00€
    100mg
    3.168,00€
  • DS34942424


    DS34942424 is an orally potent analgesic which did not exhibit mu opioid receptor agonist activity.
    Formule :C15H17FN2O
    Couleur et forme :Solid
    Masse moléculaire :260.31

    Ref: TM-T60415

    25mg
    1.369,00€
    50mg
    1.783,00€
    100mg
    2.250,00€
  • A 74273

    CAS :
    A 74273, a nonpeptidic and renin inhibitor, may be used to treat cardiovascular diseases due to renin inhibition.
    Formule :C44H74N4O8
    Degré de pureté :98%
    Couleur et forme :Solid
    Masse moléculaire :787.08

    Ref: TM-T26439

    25mg
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  • KR31173

    CAS :
    KR31173 is an AT1 antagonist with an IC50 of 3.27 nM. When labeled with the 11C isotope, KR31173 can be used as a tracer for positron emission tomography (PET). In mice, KR31173 exhibits favorable biodistribution and pharmacological characteristics. It selectively binds to organs in CD-1 mice known to have a high density of AT1 angiotensin receptors.
    Formule :C31H30N8O2
    Couleur et forme :Solid
    Masse moléculaire :546.62

    Ref: TM-T207150

    10mg
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  • 6β-Naltrexol

    CAS :
    6β-Naltrexol is a peripherally selective opioid antagonist that reduces constipation from opioids while minimizing central nervous system effects.
    Formule :C20H25NO4
    Degré de pureté :99.933%
    Couleur et forme :Solid
    Masse moléculaire :343.42

    Ref: TM-T85517

    1mg
    88,00€
    5mg
    298,00€
    10mg
    477,00€
    25mg
    799,00€
    50mg
    1.195,00€
  • Elacestrant S enantiomer dihydrochloride


    Elacestrant (RAD1901) dihydrochloride, an oral ERR degrader, has IC50 of 48 nM (ERα) and 870 nM (ERβ). Its S enantiomer has low activity.
    Formule :C30H40Cl2N2O2
    Degré de pureté :98%
    Couleur et forme :Solid
    Masse moléculaire :531.56

    Ref: TM-T11173L

    25mg
    1.872,00€
    50mg
    2.452,00€
    100mg
    3.230,00€
  • Mu opioid receptor antagonist 8

    CAS :

    Muopioid Receptor Antagonist 8 (368) serves as an antagonist to the μ-opioid receptor, significantly inhibiting the activation of Gi induced by met-enkephalin at the µOR.

    Formule :C36H35N3O4S
    Couleur et forme :Solid
    Masse moléculaire :605.75

    Ref: TM-T88728

    25mg
    1.784,00€
    50mg
    2.333,00€
    100mg
    3.039,00€
  • Riminkefon

    CAS :
    Riminkefon is a kappa opioid receptor agonist .
    Formule :C38H57N7O6
    Couleur et forme :Solid
    Masse moléculaire :707.9

    Ref: TM-T69851

    25mg
    2.313,00€
    50mg
    3.042,00€
    100mg
    4.140,00€
  • MK-6913

    CAS :
    MK-6913 is a potent and selective agonist of estrogen receptor β.
    Formule :C25H27N3O2
    Degré de pureté :98%
    Couleur et forme :Solid
    Masse moléculaire :401.5

    Ref: TM-T13136

    25mg
    2.853,00€
    50mg
    3.763,00€
    100mg
    5.220,00€
  • (Rac)-Fidarestat

    CAS :
    (Rac)-Fidarestat ((Rac)-SNK 860) is the racemic form of Fidarestat, functioning as a potent inhibitor of the enzyme aldose reductase.
    Formule :C12H10FN3O4
    Couleur et forme :Solid
    Masse moléculaire :279.224

    Ref: TM-T207035

    10mg
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    50mg
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  • CCG258747

    CAS :
    CCG258747 is a novel, selective inhibitor of the GRK2 subfamily.
    Formule :C28H27FN4O4
    Couleur et forme :Solid
    Masse moléculaire :502.54

    Ref: TM-T63411

    25mg
    1.746,00€
    50mg
    2.277,00€
  • Pentomone

    CAS :
    Pentomone (LY-113935) is an anti-androgen compound that acts as a prostate growth inhibitor.
    Formule :C24H26O5
    Couleur et forme :Solid
    Masse moléculaire :394.46

    Ref: TM-T201000

    25mg
    1.444,00€
    50mg
    1.882,00€
    100mg
    2.375,00€
  • Sunobinop

    CAS :
    Sunobinop (S 117957) is an opioid receptor-like orphan receptor (ORL1) modulator.
    Formule :C26H33N3O3
    Couleur et forme :Solid
    Masse moléculaire :435.56

    Ref: TM-T62482

    25mg
    1.927,00€
    50mg
    2.507,00€
    100mg
    3.168,00€
  • Amoitone B

    CAS :
    Amoitone B, a cystosporone B derivative, functions as an NR4A1 agonist and exhibits anticancer activity [1].
    Formule :C22H34O5
    Couleur et forme :Solid
    Masse moléculaire :378.5

    Ref: TM-T85646

    10mg
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    50mg
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  • GPR84 antagonist 3

    CAS :
    Potent GPR84 antagonist 3 (compound 42), pIC50 8.28, inhibits GTPγS, with good pharmacokinetics.
    Formule :C29H27N5O
    Couleur et forme :Solid
    Masse moléculaire :461.56

    Ref: TM-T62918

    25mg
    1.444,00€
    50mg
    1.882,00€
    100mg
    2.375,00€
  • BU72

    CAS :
    BU72 is a potent, long-lasting agonist for μ and κ opioid receptors, with partial agonistic activity at the δ opioid receptor (EC50 values of 0.054, 0.033, and 0.58 nM, respectively). It provides strong, enduring analgesic effects primarily mediated through μ opioid receptors. BU72 also exhibits a prolonged duration of activity and can partially reverse morphine-induced analgesia. It is applicable in studies of opioid dependence.
    Formule :C28H32N2O2
    Couleur et forme :Solid
    Masse moléculaire :428.57

    Ref: TM-T207187

    10mg
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    50mg
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  • JNJ-1250132

    CAS :
    JNJ-1250132 is a steroidal progesterone receptor modulator that inhibits binding of the receptor to DNA in vitro.
    Formule :C33H41NO4
    Couleur et forme :Solid
    Masse moléculaire :515.68

    Ref: TM-T27662

    25mg
    1.639,00€
    50mg
    2.142,00€
    100mg
    2.790,00€
  • ERα degrader 11

    CAS :
    ERα degrader11 (compound B16) is a selective estrogen receptor degrader designed for use as a probe in examining the ER status within ER-positive breast cancer cells.
    Formule :C28H27F3N2O3
    Couleur et forme :Solid
    Masse moléculaire :496.52

    Ref: TM-T200861

    25mg
    2.225,00€
    50mg
    2.921,00€
    100mg
    3.921,00€
  • OSU-ERb-12

    CAS :
    OSU-ERb-12 is an ERβ agonist that suppresses ovarian cancer cell proliferation both in vitro and in vivo, and decreases the expression of Snail [1] [2].
    Formule :C15H30B10O2
    Couleur et forme :Solid
    Masse moléculaire :350.51

    Ref: TM-T87077

    10mg
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    50mg
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  • ADX61623

    CAS :
    ADX61623 is an effective negative allosteric modulator (NAM) of the follicle-stimulating hormone receptor (FSHR). It also exhibits activity on the luteinizing hormone receptor (LH-R) but is inactive on the thyroid-stimulating hormone (TSH) receptor. ADX61623 can be utilized in research on estrogen-dependent diseases.
    Formule :C19H20N2O3
    Couleur et forme :Solid
    Masse moléculaire :324.37

    Ref: TM-T201265

    25mg
    1.539,00€
    50mg
    1.941,00€
    100mg
    2.451,00€
  • rel-SB-612111 hydrochloride

    CAS :
    NOP receptor antagonist
    Formule :C24H30Cl3NO
    Degré de pureté :98%
    Couleur et forme :Solid
    Masse moléculaire :454.86

    Ref: TM-T23324

    25mg
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    50mg
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  • σ1 Receptor/μ Opioid receptor modulator 2

    CAS :
    Compound 4x, also known as σ1 Receptor/μOpioid receptormodulator 2, acts as a μOR agonist and a σ1R antagonist, exhibiting a potent μOR EC50 of 0.6 nM and strong σ1R inhibitory activity (Ki: 363.7 nM). It demonstrates significant analgesic effects in various pain models.
    Formule :C23H31N3O
    Masse moléculaire :365.51

    Ref: TM-T208835

    10mg
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  • TRβ agonist 1

    CAS :
    TRβ Agonist 1, a selective and mutation-sensitive thyroid hormone receptor β (TRβ) agonist, demonstrates an EC50 value of 21 nM.
    Formule :C29H25FN2O8
    Couleur et forme :Solid
    Masse moléculaire :548.52

    Ref: TM-T63876

    25mg
    4.085,00€
    50mg
    5.710,00€
    100mg
    7.669,00€
  • Daeatal

    CAS :
    Dynorphin A ethylamide (1-9), the opioid activities were examined in the bioassays.
    Formule :C56H93N19O10
    Degré de pureté :98%
    Couleur et forme :Solid
    Masse moléculaire :1192.46

    Ref: TM-T23963

    25mg
    2.583,00€
    50mg
    3.402,00€
    100mg
    4.680,00€
  • ERRγ agonist-1


    ERRγ agonist-1 can be used in neuropsychological disorders research.
    Formule :C17H21N5O
    Couleur et forme :Solid
    Masse moléculaire :311.38

    Ref: TM-T60772

    25mg
    1.369,00€
    50mg
    1.783,00€
    100mg
    2.250,00€
  • Estrogen receptor-agonist-1

    CAS :
    Estrogen receptor-agonist-1 (compound 4e) is an estrogen receptor (ER) agonist that binds to ERα with high affinity.
    Formule :C24H22N2O2
    Couleur et forme :Solid
    Masse moléculaire :370.444

    Ref: TM-T204741

    10mg
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    50mg
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  • ACT 178882

    CAS :
    ACT 178882 is a new Renin inhibitor (IC50: 1.4 nM).
    Formule :C33H38Cl3N3O4
    Degré de pureté :98%
    Couleur et forme :Solid
    Masse moléculaire :647.03

    Ref: TM-T14123

    25mg
    2.718,00€
    50mg
    3.582,00€
    100mg
    4.950,00€
  • SDM25N hydrochloride

    CAS :
    δ receptor antagonist
    Formule :C26H27ClN2O3
    Degré de pureté :98%
    Couleur et forme :Solid
    Masse moléculaire :450.96

    Ref: TM-T23341

    25mg
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    50mg
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  • BNTX maleate

    CAS :
    δ1 opioid receptor antagonist
    Formule :C31H31NO8
    Degré de pureté :98%
    Couleur et forme :Solid
    Masse moléculaire :545.58

    Ref: TM-T22613

    1mg
    87,00€
    5mg
    333,00€
    10mg
    627,00€
  • Fonsartan free acid

    CAS :
    Fonsartan: Angiotensin receptor blocker, halts angiotensin II effects on rat vascular cells.
    Formule :C26H32N4O5S2
    Degré de pureté :98%
    Couleur et forme :Solid
    Masse moléculaire :544.69

    Ref: TM-T27347

    25mg
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    50mg
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  • FSH receptor antagonist 1

    CAS :
    FSH receptor antagonist 1 (compound 10) is a potent antagonist of the G(s) protein-coupled human follicle-stimulating hormone (FSH) receptor. It exhibits an IC50 value of 28 nM in cell lines expressing the human FSH receptor. This compound significantly inhibits follicle growth and ovulation in in vitro mouse models.
    Formule :C33H32N2O2
    Couleur et forme :Solid
    Masse moléculaire :488.619

    Ref: TM-T204299

    10mg
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    50mg
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  • MB-07344 sodium


    "MB-07344 sodium is a TR-β agonist with a 2.17 nM Ki, boosts Atorvastatin's cholesterol-lowering effects in various animals."
    Formule :C19H25NaO5P
    Degré de pureté :98%
    Couleur et forme :Solid
    Masse moléculaire :387.36

    Ref: TM-T11954L

    25mg
    1.872,00€
    50mg
    2.452,00€
    100mg
    3.230,00€
  • ZD 7155 hydrochloride

    CAS :
    ZD 7155 hydrochloride is an angiotensin II receptor type 1 (AT1 receptor) antagonist.
    Formule :C26H27ClN6O
    Degré de pureté :99.8%
    Couleur et forme :Solid
    Masse moléculaire :474.98

    Ref: TM-T13390

    1mg
    42,00€
    5mg
    88,00€
    10mg
    135,00€
    25mg
    235,00€
    50mg
    396,00€
    100mg
    635,00€
    200mg
    887,00€
    1mL*10mM (DMSO)
    90,00€
  • L-371,257

    CAS :
    L-371,257 is a competitive antagonist of oxytocin receptor with pA2 of 8.4 and Ki of 19 nM. L-371,257 shows a Ki of 3.7 nM for vasopressin receptor 1a.
    Formule :C28H33N3O6
    Degré de pureté :99.79%
    Couleur et forme :Solid
    Masse moléculaire :507.58

    Ref: TM-T15682

    1mg
    38,00€
    5mg
    86,00€
    10mg
    124,00€
    25mg
    241,00€
    50mg
    355,00€
    100mg
    507,00€
  • GLPG0974

    CAS :
    GLPG0974 is an antagonist of FFA2/GPR43 with IC50 of 9 nM.
    Formule :C25H25ClN2O4S
    Degré de pureté :99.8%
    Couleur et forme :Solid
    Masse moléculaire :484.99

    Ref: TM-T15388

    1mg
    56,00€
    5mg
    119,00€
    10mg
    187,00€
    25mg
    376,00€
    50mg
    560,00€
    1mL*10mM (DMSO)
    126,00€
  • Cort108297

    CAS :
    Cort108297: selective GR modulator/antagonist, high GR affinity (Ki: 0.45nM), no other steroid receptor affinity.
    Formule :C26H25F4N3O3S
    Degré de pureté :98.36% - 99.94%
    Couleur et forme :Solid
    Masse moléculaire :535.55

    Ref: TM-T15000

    1mg
    274,00€
    5mg
    622,00€
    10mg
    908,00€
    25mg
    1.415,00€
    50mg
    1.882,00€
    100mg
    2.745,00€
    1mL*10mM (DMSO)
    747,00€
  • (E/Z)-GSK5182

    CAS :
    GSK5182 is a racemic mix of (E/Z) isomers, a selective ERRγ inverse agonist (IC50: 79 nM), and induces ROS in liver cancer.
    Formule :C27H31NO3
    Degré de pureté :97.58%
    Couleur et forme :Solid
    Masse moléculaire :417.54

    Ref: TM-T7709

    1mg
    81,00€
    5mg
    170,00€
    10mg
    274,00€
    25mg
    502,00€
    50mg
    747,00€
    100mg
    1.121,00€
    1mL*10mM (DMSO)
    187,00€
  • LSZ-102

    CAS :
    LSZ-102 is an effective and selective degrader of estrogen receptor (IC50 = 0.2 nM) and can be used in studies about ERα positive breast cancer.
    Formule :C25H17F3O4S
    Degré de pureté :98.56%
    Couleur et forme :Solid
    Masse moléculaire :470.46

    Ref: TM-T15788

    1mg
    88,00€
    5mg
    187,00€
    10mg
    303,00€
    25mg
    512,00€
    50mg
    687,00€
    1mL*10mM (DMSO)
    188,00€
  • ML314

    CAS :
    ML314 is a brain-permeable nonpeptide β-inhibin-biased neurotensin NTR1 receptor agonist (EC50: 1.9 μM), a biased neurotensin receptor ligand for methamphetamine abuse that inhibits NTR2 and GPR35.
    Formule :C24H28N4O3
    Degré de pureté :99.52%
    Couleur et forme :Solid
    Masse moléculaire :420.504

    Ref: TM-TQ0075

    Produit arrêté
  • Mapracorat

    CAS :
    Mapracorat (ZK-245186, BOL-303242X) is a selective glucocorticoid receptor agonist,anti-inflammatory agent for atopic dermatitis and allergic conjunctivitis.
    Formule :C25H26F4N2O2
    Couleur et forme :Solid
    Masse moléculaire :462.48

    Ref: TM-T13451L

    Produit arrêté
  • PSN632408

    CAS :
    PSN632408 is an optimized agonist of GPR119 receptors that display similar potency to OEA at both recombinant mouse and human GPR119 receptors (EC50: 5.6 and 7.9 uM, respectively).
    Formule :C18H24N4O4
    Degré de pureté :98%
    Couleur et forme :Solid
    Masse moléculaire :360.41

    Ref: TM-T16678

    Produit arrêté
  • (S)-Mapracorat

    CAS :
    (S)-Mapracorat is a selective and less active agonist of the glucocorticoid receptor.
    Formule :C25H26F4N2O2
    Couleur et forme :Solid
    Masse moléculaire :462.48

    Ref: TM-T13451

    Produit arrêté
  • Mouse MDA(Malondialdehyde) ELISA Kit


    This assay employs the competitive inhibition enzyme immunoassay technique. The microtiter plate provided in this kit has been pre-coated with Mouse MDA protein. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Mouse MDA. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of Mouse MDA in the samples is then determined by comparing the OD of the samples to the standard curve.

  • Rat VLDL(Very Low Density Lipoprotein) ELISA Kit


    The test principle applied in this kit is Sandwich enzyme immunoassay. The microtiter plate provided in this kit has been pre-coated with an antibody specific to Rat VLDL. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Rat VLDL. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added, only those wells that contain Rat VLDL, biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of Rat VLDL in the samples is then determined by comparing the OD of the samples to the standard curve.

  • Relacorilant

    CAS :

    Relacorilant is an oral glucocorticoid receptor antagonist with Ki of 7.2 nM, potential for treating Cushing's syndrome.

    Formule :C27H22F4N6O3S
    Degré de pureté :98.53% - 99%
    Couleur et forme :Solid
    Masse moléculaire :586.56
  • Horse IGF1(Insulin Like Growth Factor 1) ELISA Kit


    The test principle applied in this kit is Sandwich enzyme immunoassay. The microtiter plate provided in this kit has been pre-coated with an antibody specific to Horse IGF1. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Horse IGF1. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added, only those wells that contain Horse IGF1, biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of Horse IGF1 in the samples is then determined by comparing the OD of the samples to the standard curve.

  • PF-998425

    CAS :
    non-steroidal androgen receptor (AR) antagonist
    Formule :C14H14F3NO
    Degré de pureté :98%
    Couleur et forme :Solid
    Masse moléculaire :269.26

    Ref: TM-T23141

    Produit arrêté
  • Phosphoramidon Disodium

    CAS :
    Phosphoramidon Disodium (Phosphoramidon Disodium Salt) Salt is a metalloendopeptidase inhibitor, widely used as a biochemical tool.
    Formule :C23H34N3Na2O10P
    Degré de pureté :98%
    Couleur et forme :Solid
    Masse moléculaire :588.48
  • GPR109 receptor agonist-2

    CAS :
    Compound 5, a selective GPR109a agonist, exhibits a pEC50 value of 5.53 [1].
    Formule :C7H10N2O2
    Couleur et forme :Solid
    Masse moléculaire :154.17

    Ref: TM-T78100

    Produit arrêté
  • 21-Acetoxypregna-1,4,9(11),16-tetraene-3,20-dione


    21-Acetoxypregna-1,4,9(11),16-tetraene-3,20-dione is a valuable organic compound for life sciences research [Catalog No.: T67476, CAS No.: 37413-91-5].
    Formule :C23H26O4
    Couleur et forme :Solid
    Masse moléculaire :366.457

    Ref: TM-T67476

    Produit arrêté
  • ERB-196

    CAS :
    Erb-196 is an estrogen receptor-receptor agonist with non-steroidal selectivity.
    Formule :C17H10FNO2
    Degré de pureté :98%
    Couleur et forme :Solid
    Masse moléculaire :279.27

    Ref: TM-T11222

    Produit arrêté
  • Omzotirome

    CAS :
    Omzotirome (TRC150094) is a functional analog of iodothyronines and holds potential for research on hyperlipidemia (WO2008149379).
    Formule :C19H24N2O3
    Couleur et forme :Solid
    Masse moléculaire :328.412

    Ref: TM-T38483

    Produit arrêté
  • AZD9496 maleate

    CAS :
    AZD9496 maleate is a highly potent and selective antagonist of the estrogen receptor alpha (ERα), exhibiting an IC50 value of 0.28 nM. This compound, AZD9496 maleate, is an orally bioavailable selective estrogen receptor degrader (SERD).
    Formule :C29H29F3N2O6
    Couleur et forme :Solid
    Masse moléculaire :558.554

    Ref: TM-T39118

    Produit arrêté
  • L-372662

    CAS :
    L-372662 is bioactive chemical.
    Formule :C33H38N4O6
    Couleur et forme :Solid
    Masse moléculaire :586.68

    Ref: TM-T32497

    Produit arrêté
  • Pamoic acid

    CAS :

    Pamoic acid is the orphan G protein-coupled receptor GPR35 agonist. Pamoic acid activates ERK and beta-arrestin2 and causes antinociceptive activity.

    Formule :C23H16O6
    Degré de pureté :99.99%
    Couleur et forme :Fine Yellow Powder
    Masse moléculaire :388.37

    Ref: TM-T8353

    Produit arrêté
  • SR17018

    CAS :

    SR17018 is an mu-opioid-receptor (MOR) agonist, binding with GTPγS, with an EC50 of 97 nM.

    Formule :C19H18Cl3N3O
    Degré de pureté :99.89%
    Couleur et forme :Solid
    Masse moléculaire :410.72

    Ref: TM-T4407

    1mL*10mM (DMSO)
    Arrêté
    Produit arrêté
  • Cebranopadol

    CAS :

    Cebranopadol (GRT6005) is an analgesic NOP and opioid receptor agonist with Kis of 0.9 nM, 0.7 nM, 2.6 nM, 18 nM for human NOP, μ-opioid (MOP), κ-opioid (KOP)

    Formule :C24H27FN2O
    Degré de pureté :98.32% - 99.78%
    Couleur et forme :Solid
    Masse moléculaire :378.48
  • Ceronapril

    CAS :
    Ceronapril (SQ 29852) is an orally active and potent angiotensin-converting enzyme (ACE) inhibitor (IC50 : 36 nM) for the study of dementia and hypertension.
    Formule :C21H33N2O6P
    Degré de pureté :97.94%
    Couleur et forme :Solid
    Masse moléculaire :440.47
  • Bromadoline maleate

    CAS :
    Bromadoline is an opioid analgesic selective for the μ-opioid receptor.
    Formule :C19H25BrN2O5
    Degré de pureté :98%
    Couleur et forme :Solid
    Masse moléculaire :441.322
  • SR14150

    CAS :
    SR14150 is a partial agonist of high-affinity NOP receptor.
    Formule :C21H30N2O
    Degré de pureté :98%
    Couleur et forme :Solid
    Masse moléculaire :326.48
  • Tirzepatide acetate

    CAS :

    Cymit Quimica provides this product solely for uses within the scope of any statute or law providing for an immunity, exemption, or exception to patent infringement (“Exempted Uses”), including but not limited to 35 U.S.C. § 271(e)(1) in the United States, the Bolar type exemption in Europe, and any corresponding exception to patent infringement in any other country. It is the sole responsibility of the purchaser or user of this product, and the purchaser or user of this product agrees to engage only in such Exempted Uses, and to comply with all applicable intellectual property laws and/or regulations. The purchaser of this product agrees to indemnify Cymit Quimica against all claims in connection with the performance of the respective commercial agreement (e.g. supply agreement) and possible infringements of intellectual property rights.

    Degré de pureté :Min. 95%
  • MOR agonist-1

    CAS :

    MOR Agonist-1 is a μ-opioid receptor (MOR) agonist noted for its potent analgesic properties and is utilized in research concerning pain and associated

    Formule :C22H26ClFN2O2
    Degré de pureté :98%
    Couleur et forme :Solid
    Masse moléculaire :404.91
  • Estrogen receptor modulator 8

    CAS :

    Estrogen Receptor Modulator 8 (compound 4) is an orally active inhibitor targeting Estrogen Receptor/ERR α with potent efficacy (IC50 = 0.437 nM in MCF-7 cells

    Formule :C25H24F4N2O2
    Degré de pureté :98%
    Couleur et forme :Solid
    Masse moléculaire :460.46
  • ALS-I-41

    CAS :
    ALS-I-41 is a novel, potent and selective antagonist of oxytocin receptor.
    Formule :C30H38FN3O6S
    Degré de pureté :98%
    Couleur et forme :Solid
    Masse moléculaire :587.7