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dimeric

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  • Inhibitors & Agonists
    42
    TargetMol | Inhibitors_Agonists
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    3
    TargetMol | Inhibitory_Antibodies
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    TargetMol | Dye_Reagents
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    TargetMol | Inhibitors_Agonists
BMS-202
PD1-PDL1 inhibitor 2, PD-1 PD-L1 inhibitor 2
T31461675203-84-5
BMS-202 (PD1-PDL1 inhibitor 2) is an inhibitor of the PD-1 (Programmed death- 1) PD-Ll (Programmed death-ligand 1) protein protein interaction.
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TargetMol | Inhibitor Hot
Dimeric coniferyl acetate
TN3869184046-40-0
Dimeric coniferyl acetate has anti-inflammary activity, it shows strong NO inhibition with IC50 values of 27.1 uM in lipopolysacchalide (LPS)-activated murine macrophage-like J774.1 cells. It exhibits significant inhibitory effects on the nitric oxide pro
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Dupilumab
SAR-231893, REGN-668
T136661190264-60-8
Dupilumab (REGN-668) is a fully human monoclonal antibody targeting the alpha subunit of the interleukin-4 receptor, thereby inhibiting IL-4 and IL-13 signaling. As a systemic immunomodulator, it has demonstrated efficacy in improving atopic dermatitis.
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TargetMol | Inhibitor Hot
S 0960
S0960
T70688142974-51-4In house
S 0960 is a dimeric bile acid analog, a specific inhibitor of the sodium-dependent bile salt transporter in the ileum, used in metabolic disease research.
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10-14 weeks
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G-9807
G9807, G 9807
T84372 In house
G-9807 significantly increases the RNase activity of IRE1-KR-0P by stabilizing the active dimeric unit, which acts as a variable activator of RNase.
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Pantethine
Pantosin, Pantomin, D-Pantethine, LBF disulfide, Bis-pantethine, Pantetina
T097816816-67-4
Pantethine (Pantomin) (Bis-pantethine) is a dimeric form of vitamin B5. Pantethine is less stable than pantothenic acid and tends to decompose over time if it is not kept refrigerated, so most vitamin B5 supplements are in the form of calcium pantothenate. It is available as a dietary supplement and is used to treat acne and improve the blood-cholesterol profile.
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Enpp-1-IN-22
T2004742954111-09-0
Enpp-1-IN-22 is a potent oral bioavailable prodrug of the ENPP1 inhibitor dimeric paraformaldehyde ester, exhibiting anticancer activity.
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3-6 months
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DOTAGA.(SA.FAPi)2 TFA
T200872
DOTAGA.(SA.FAPi)2 TFA is an effective dimeric fibroblast activation protein inhibitor (FAPi). This compound holds potential for use in cancer diagnostic research.
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ART838
ART-838, ART 838
T201951676620-45-4
ART838 is a dimeric pimeloyl urea compound notable for its potent anti-leukemic activity and favorable pharmacological properties. In vitro, ART-838 exhibits submicromolar inhibitory concentrations against all leukemia cell lines, demonstrating anti-leukemic efficacy 88 times greater than artemether. This compound remains in the body for extended periods and works synergistically with other anti-leukemic agents and novel kinase inhibitors to suppress leukemia cell growth. In immunodeficient NOD-SCID-IL2Rgnull (NSG) mice, ART-838 attains a plasma half-life longer than that of artemether, sustaining effective anti-leukemic concentrations for over 8 hours. Intermittent ART-838 treatment notably inhibited the growth of acute leukemia xenografts and primary grafts in NSG mice, surpassing the efficacy of artemether.
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ART631
ART-631, ART 631
T2019631426680-31-0
ART631 is a dimeric artemisinin compound with strong anti-leukemia activity and favorable pharmacological properties, characterized by a structure connected via a two-carbon chain.
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DQ661
T2043152027551-01-3
DQ661 is a potent inhibitor of PPT1 and a dimeric quinacrine autophagy (autophagy) inhibitor. It effectively suppresses the activity of mTORC1 and reduces protein expression levels of pS6K T389 and pS6 S240-244. Additionally, DQ661 exhibits anticancer properties.
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10-14 weeks
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bis(7)-Tacrine
T22048224445-12-9
Bis(7)-tacrine dihydrochloride is a dimeric AChE inhibitor derived from tacrine with potential to treat Alzheimer's disease, prevents glutamate-induced neuronal apoptosis by blocking NMDA receptors, and is a potent GABA A receptor antagonist[1] [2] [3].
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6-8 weeks
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Picrasidine N
Picrasidine-N,PicrasidineN
T28415101219-62-9
Picrasidine N is a naturally occurring dimeric alkaloid and a PPARβ/δ agonist.
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Ioforminol
GE-145,GE145,AN 113111,AN113111,AN-113111,GE 145
T321771095110-48-7
Ioforminol, also known as GE-145 and AN-113111, is a new low-osmolar dimeric radiographic contrast agent. GE-145 exhibits similar preclinical properties to other dimeric radiographic contrast media. In addition, the low osmolality enables an iso-osmolar f
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Kopsoffine
T3241389783-67-5
Kopsoffine is a new dimeric indole alkaloid of pleiomutine type from kopsia offcinalis.
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Maesol
T33162119766-98-2
Maesol is a novel dimeric phenol isolated from seeds of Maesa montana and Maesa indica.
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Lys05
Lys01 trihydrochloride
T34371391426-24-6
Lys05, or Lys01 trihydrochloride, is a potent, water soluble lysosomal autophagy inhibitor. Lys05 is a previously undescribed dimeric chloroquine which more potently accumulates in the lysosome and blocks autophagy compared with HCQ. Lys05 produced more p
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TargetMol | Inhibitor Sale
AZD5582 dihydrochloride
AZD 5582 dihydrochloride
T362011883545-51-4
Dimeric Smac mimetic; potent inhibitor of X-linked (XIAP) and cellular (cIAP) inhibitor of apoptosis protein (IC50 values are 15, 15 and 21 nM for XIAP, cIAP1 and cIAP2 respectively). Binds to the BIR3 domain of XIAP to prevent interaction with caspase-9. Causes degradation of cIAP1 and cIAP2 and induces apoptosis in MDA-MB-231 breast cancer cells. Causes tumor regression in MDA-MB-231 xenograft-bearing mice. Hennessy et al (2013) Discovery of a novel class of dimeric Smac mimetics as potent IAP antagonists resulting in a clinical candidate for the treatment of cancer (AZD5582). J.Med.Chem. 56 9897 PMID:24320998
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Remisporine B
T37288571194-06-4
Remisporine B is a polyketide and derivative of remisporine A that has been found inPenicilliumand has immunosuppressant activity.1,2It inhibits LPS- or concanavalin A-induced proliferation of isolated mouse splenic lymphocytes (IC50s = 30.1 and 32.4 μg/ml, respectively).1 1.Liu, H., Chen, S., Liu, W., et al.Polyketides with immunosuppressive activities from mangrove endophytic fungus Penicillium sp. ZJ-SY2Mar. Drugs14(12)217(2016) 2.Kong, F., and Carter, G.T.Remisporine B, a novel dimeric chromenone derived from spontaneous Diels-Alder reaction of remisporine ATetrahedron Lett.44(15)3119-3122(2003)
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Terazosin dimer impurity dihydrochloride
T378171486464-41-8
Terazosin dimer impurity dihydrochloride, a dimeric form of Terazosin, is a chemical impurity found in Terazosin. Terazosin itself is a derivative of quinazoline and acts as a competitive and orally active α1-adrenoceptor antagonist[1].
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Pyrrole-2-carboxaldehyde
T383951003-29-8
Pyrrole-2-carboxaldehyde exhibits distinctive vibrational and electronic properties which serve to validate its dimeric state in the solid phase and monomeric state in the solution phase.
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7-10 days
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LasR-IN-3
T61305
LasR-IN-3, a chemical compound, acts as an inhibitor of LasR in Pseudomonas aeruginosa. It induces structural instability in LasR and causes complete dissociation of its functioning dimeric form [1].
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10-14 weeks
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IMP-321
T68322928150-91-8
IMP-321 is a soluble dimeric recombinant form of LAG-3 and first-in-class antigen presenting cell activator.
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10-14 weeks
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TLN-232
T70418158899-10-6
TLN-232, also known as CAP-232, is a synthetic cyclic heptapeptide with potential antineoplastic activity. Pyruvate kinase (PK) inhibitor TLN-232 targets pyruvate kinase M2 (M2PK), which may disrupt tumor cell anaerobic glycolysis. M2PK is a dimeric isoform of PK and the predominant PK isoform found in tumor cells.
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10-14 weeks
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