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Results for "

diastereomer

" in TargetMol Product Catalog
  • Inhibitors & Agonists
    20
    TargetMol | All_Pathways
  • PROTAC Products
    3
    TargetMol | PROTAC
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    5
    TargetMol | Natural_Products
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    TargetMol | Standard_Products
cis-Tadalafil
Tadalafil specified impurity A, (-)-Tadalafil (6R ,12aS) diastereomer
T20024171596-27-3
cis-Tadalafil (cis-IC-351) is a potent PDE5 inhibitor with an IC50 value of 0.09 μM that can be used to study arterial hypertension.
  • $176
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Epi-galantamine
T136811668-85-5
Epi-galantamine, a diastereomer of galantamine, is an alkaloid extracted from the bulbs and flowers of the Caucasian snowdrop (Galanthus woronowii). It acts as an AChE inhibitor, featuring an EC50 of 45.7 μM.
  • $126
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Yamogenin
T7529512-06-1
Yamogenin is a diastereomer of diosgenin, which we have identified as the compound responsible for the anti-hyperlipidemic effect of fenugreek.
  • $48
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YN14 (mixture of diastereomers)
T2122103053689-54-3
YN14, a mixture of diastereomers, is a PROTAC (proteolysis-targeting chimera) specifically designed for the KRASG12C protein. It acts as an efficient and selective degrader of KRASG12C, forming a stable KRASG12C:YN14:VHL ternary complex with low binding free energy (ΔG). YN14 exhibits antiproliferative properties, significantly inhibiting the growth of cancer cells with the KRASG12C mutation.
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Pinaverium-d4 Bromide (Mixture of Diastereomers)
TMIJ-0270
Pinaverium-d4 Bromide (Mixture of Diastereomers) is a deuterated compound of Pinaverium Bromide. Pinaverium Bromide has a CAS number of 53251-94-8. Pinaverium bromide is an calcium channel blocker with Antispasmodic and effectively relieves pain, diarrhea and intestinal discomfort.
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20 days
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Nadolol-d9 (Mixture of Diastereomers)
TMIJ-03171432056-38-6
Nadolol-d9 (Mixture of Diastereomers) is a deuterated compound of Nadolol. Nadolol has a CAS number of 42200-33-9. Nadolol is a non-selective beta-adrenergic antagonist with antihypertensive and antiarrhythmic activities. Nadolol competitively blocks beta-1 adrenergic receptors located in the heart and vascular smooth muscle, inhibiting the activities of the catecholamines epinephrine and norepinephrine and producing negative inotropic and chronotropic effects. This agent exhibits antiarrhythmic activity via the impairment of atrioventricular (AV) node conduction and a corresponding reduction in sinus rate. In the kidney, inhibition of the beta-2 receptor within the juxtaglomerular apparatus results in the inhibition of renin production and a subsequent reduction in angiotensin II and aldosterone levels, thus inhibiting angiotensin II-dependent vasoconstriction and aldosterone-dependent water retention.
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20 days
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rac-Brivaracetam-d7 (Mixture of Diastereomers)
TMIJ-03181202896-51-2
rac-Brivaracetam-d7 (Mixture of Diastereomers) is a deuterated compound of rac-Brivaracetam. rac-Brivaracetam has a CAS number of 357335-87-6.
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20 days
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Juvenile hormone B 3 (mixture of diastereomers)
Juvenile hormone III bisepoxide, Juvenile hormone bisepoxide, JHB3
TN11536120293-93-8
Juvenile hormone B 3 (Juvenile hormone III bisepoxide) (mixture of diastereomers) is a sesquiterpenoid hormone. It can be isolated from the corpora allata (CA) of higher dipteran insects such as fruit flies and Drosophila melanogaster. This hormone exhibits anti-metamorphic activity and induces the expression of Kr-h1 by directly interacting with juvenile hormone (JH) receptors (Met and Gce). Juvenile hormone B 3 (mixture of diastereomers) is applicable in insect lethality studies.
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10-14 weeks
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Sauchinone
T6S1572177931-17-8
1. Sauchinone is a useful adjunctive treatment for bacterial infection. 2. Sauchinone, an active lignan found in Saururus chinensis, to regulate the activation of HSCs, to prevent liver fibrosis, and to inhibit oxidative stress in vivo and in vitro. 3. Sa
  • $29
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Sofosbuvir impurity F
Sofosbuvir 3',5'-Bis-(S)-phosphate
T129611337482-17-3
Sofosbuvir impurity F (Sofosbuvir 3',5'-Bis-(S)-phosphate) is both a diastereomer of Sofosbuvir and an impurity of Sofosbuvir which is an inhibitor of HCV RNA replication.
  • $562
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Sofosbuvir impurity G
T129621337482-15-1
Sofosbuvir impurity G is a diastereoisomer of Sofosbuvir.Sofosbuvir is an HCV RNA replication inhibitor, with potent anti-hepatitis C virus activity.
  • $1,160
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(S)-AL-8810
T2095191224444-55-6
(S)-AL 8810 is an 11β-fluoro analog of PGF2α, serving as a potent and selective antagonist for FP receptors. It is the C-15 diastereomer of AL 8810, with an inverted (S) configuration at C-15 compared to AL 8810, where the "natural" configuration is 15-(R).
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10-14 weeks
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6-epi-COTC
T210439959150-61-9
6-epi-COTC is a diastereomer of a metabolite produced by Streptomyces, exhibiting anticancer activity.
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10-14 weeks
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PROTAC SGK3 degrader-2
T2125602381196-78-5
PROTACSGK3degrader-2 is the cis-diastereomer of PROTACSGK3degrader-1 (SGK3-PROTAC1), featuring a cis-hydroxy group in its VH032 section, which prevents binding to the VHL E3 ligase. This compound inhibits SGK3, SGK1, and S6K1 with IC50 values of 0.6 μM, 1.4 μM, and 1.7 μM, respectively, but does not degrade SGK3. It serves as a control compound for studying the specific degradation effects mediated by SGK3-PROTAC1.
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LLY-284
T223562226515-75-7
LLY-284, the diastereomer of LLY-283, serves as a selective and potent SAM-competitive chemical probe for PRMT5. Unlike the highly active LLY-283, LLY-284 exhibits significantly lower activity and is used as a negative control for LLY-283.
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3-6 months
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Golgicide A-1
Golgicide A-1, GCA-1
T388171394285-49-4
Golgicide A-1 (GCA-1) is a moderately potent cis-diastereomer variant of Golgicide A (GCA), designed specifically to inhibit mosquito reproduction.
  • $416
7-10 days
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dTAGV-1-NEG TFA
T74412
dTAGV-1-NEG TFA, a diastereomer, serves as the heterobifunctional negative control for dTAGV-1. It acts specifically as an FKBP12 F36V-selective degrader [1].
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Yamogenin (Standard)
TMSM-2800512-06-1
Yamogenin (Standard) is a reference standard for research and analysis in studies involving Yamogenin. Yamogenin is a diastereomer of diosgenin, which we have identified as the compound responsible for the anti-hyperlipidemic effect of fenugreek.
  • $1,050
7-10 days
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(3S)-Citramalyl-CoA
(3S)-Citramalyl-coenzyme A
TXB-00765940911-57-9
(3S)-Citramalyl-CoA ((3S)-Citramalyl-coenzyme A) is the (3S)-diastereomer of Citramalyl-CoA.
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iGePhos1
TYD-02799
iGePhos1 is an inactive diastereomer of GePhos1, utilized as a non-binding negative control. Notably, iGePhos1 does not have the capability to recruit phosphatase.
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