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Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T77614 | DpC | Others | |
DPC is an antitumor compound that inhibits cancer cell proliferation with an IC50 of 0.007-0.096 μM.DPC is involved in a variety of anticancer therapies and can be used in cancer research. | |||
TP1906L1 | DPC AJ1951 acetate | Thyroid hormone receptor(THR) | |
DPC-AJ1951 acetate, a 14 amino acid peptide that acts as a potent agonist of the parathyroid hormone (PTH)/PTH-related peptide receptor (PPR). And characterized the activity of DPC-AJ1951 acetate in ex vivo and in vivo a... | |||
T37409 | DPC-AJ1951 (trifluoroacetate salt) | DPC-AJ1951 (trifluoroacetate salt) | |
DPC-AJ1951 is a peptide agonist of the parathyroid hormone (PTH)/PTH-related peptide receptor (PPR; EC50 = 0.15 nM in HEK293 cells expressing human PPR). It induces cAMP production in SAOS-2 and UMR106 cells that endogen... | |||
TP1906 | DPC-AJ1951 | DPC AJ1951 | |
Potent 14 amino acid peptide agonist of the parathyroid hormone (PTH) receptor (EC50 = 26 nM). | |||
T27201 | DPC-082 | DPC 082 | |
DPC-082 is a reverse transcriptase inhibitor. DPC-082 exhibits low-nanomolar potency toward wild-type virus, L100I and K103N single-mutation variants, and multiplies amino acid-substituted HIV type 1 mutants. | |||
T30531 | BMS-561392 | DPC333,DPC 333,DPC-333,BMS561392,BMS 561392 | TNF |
BMS-561392 (DPC333) is a tumor necrosis factor-α ( TNF-α) Invertase inhibitor. | |||
T27202 | DPC-423 | DPC-423 Free | |
DPC-423 is a factor Xa inhibitor potentially for the treatment of thrombosis. | |||
T27204 | DPC-963 | DMP 963,DMP963,DMP-963,DPC 963,DPC963 | |
DPC-963 is a RNA-directed DNA polymerase inhibitor. | |||
T15163 | DPC-681 | DPH-153893 | Others |
DPC-681 is a potent and selective HIV protease inhibitor (IC90s: 4 to 40 nM for wild-type HIV-1). | |||
T27203 | DPC-961 | DMP 961,DMP-961,DMP961 | |
DPC-961, a reverse transcriptase inhibitor, is used potentially for the treatment of HIV infection. | |||
T19729 | Dodecylphosphocholine | DPC,n C12PC,Foscholine-12,DDPPC,nC12PC,n-C12PC | Others |
Dodecylphosphocholine (DPC) is a substrate-type inhibitor of pancreas phospholipase A2. Dodecylphosphocholine is a detergent. | |||
T27154 | Dexelvucitabine | D-D-4FC,DPC-817,RVT,beta-D-D-4FC,DFC | Reverse Transcriptase |
Dexelvucitabine (RVT), a nucleoside reverse transcriptase inhibitor, is used potentially for the treatment of HIV infection. | |||
T75942 | DPC-AJ1951 TFA | ||
DPC-AJ1951 TFA, a 14-amino acid peptide, functions as a potent agonist for the parathyroid hormone (PTH)/PTH-related peptide receptor (PPR). It has been characterized for its activity through ex vivo and in vivo bone res... | |||
T26851 | BMS-561390 | DPC083,DPC 083,DPC-083 | |
BMS-561390, a reverse transcriptase inhibitor, is used potentially for the treatment of HIV infection. | |||
T27289 | Etacstil | GW 5638,GW-5638,GW5638,DPC974,DPC 974,DPC-974 | |
GW5638 is a estrogen receptor ligand. GW5638 is a prodrug of its active metabolite GW7604. GW5638 appears to act as an antagonist in these in vitro systems, although in a manner distinct from other known ER modulators. G... | |||
T12694 | Razaxaban hydrochloride | BMS 561389 hydrochloride,DPC 906 hydrochloride | Others |
Razaxaban hydrochloride is a highly potent, selective and orally active inhibitor of factor Xa(Ki of 0.19 nM),has strongly antithrombotic activity. | |||
T21653 | 1,4-DPCA | HIF/HIF Prolyl-Hydroxylase | |
1,4-DPCA is an inhibitor of prolyl-hydroxylase with an IC50 of 2.4 µM for collagen hydroxylation in human foreskin fibroblasts and 60 μM for factor inhibiting HIF (FIH). | |||
T22744 | DPCPX | PD 116948 | Adenosine Receptor |
DPCPX (PD 116948) is an A1 adenosine receptor antagonist | |||
T36796 | 1,4-DPCA ethyl ester | ||
1,4-DPCA ethyl ester, the ethyl ester derivative of 1,4-DPCA, acts as an inhibitor of the enzyme factor inhibiting HIF (FIH)[1]. | |||
T36745 | CDPCP | ||
cDPCP is a platinum-containing DNA-crosslinking agent.1Unlike cisplatin or oxaliplatin , cDPCP forms monofunctional DNA adducts. It is transported into cells by organic cation transporter 1 (OCT1) and OCT2, inhibiting pr... |