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| Cat. No. | Product Name | Field of Application | Chemical Structure |
|---|---|---|---|
| DCY-134 | O-diacetyldaurisoline |
>98%,Standard References
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| DCZ-251 | Sanguinarine Sulfate |
>98%,Standard References
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| DCF-013 | 3,′6-d isinapoyl sucrose |
>98%,Standard References
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| DCQ-066 | 13-Dehydroxyindaconintine |
>98%,Standard References
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| DCX-046 | Sipeimine-3β-D-glucoside |
>98%,Standard References
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| DCH-060 | Quercetin-3-O-β-D-glucopyranosyl-7-O-β-D-gentiobiosid |
>98%,Standard References
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| DCQ-082 | 25-OH-PPD |
>98%,Standard References
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| DCY-121 | 20(R)Protopanaxdiol |
>98%,Standard References
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| DCX-035 | Dihydrocucurbitacin F |
>98%,Standard References
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| DCY-150 | Icarisid I |
>98%,Standard References
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| DCY-135 | Bullatine G |
>98%,Standard References
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| DCY-159 | Isosinensetin;3’,4’ ,5,7,8-pentamethoxyflavone |
>98%,Standard References
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| DCD-075 | 6-O-Caffeoylerigeroside |
>98%,Standard References
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| DCJ-026 | Worenine chloride |
>98%,Standard References
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| DCJ-052 | 7-O-Methylchrysin |
>98%,Standard References
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| DCM-065 | 3-O-galloylmucic acid |
>98%,Standard References
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| DCZ-121 | Vitamin B6 |
>98%,Standard References
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| DC12522 | MKK7-COV-3 Featured |
MKK7-COV-3 (MKK7 Covalen inhibitor 3) is a potent, selective, covalent MKK7 inhibitor with in vitro IC50 of 5 nM, displays >1,000-fold selectivity over MKK4 (IC50=7.81 uM), shows EC50 of 1.3 uM for reduction of p-JNK in ICW assays in Beas2B cell line, wit
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| DC22215 | RO 27-3225 Featured |
RO 27-3225 (RO27-3225, RO 273225) is a potent, selective melanocortin melanocortin receptor MC4R agonist with EC50 of 1 nM, >30-fold selectivity over MC3R.
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| DC11869 | RORγt inhibitor 1 |
A potent, selective, orally bioavailable RORγt inverse agonist with IC50 of 17 nM in TR-FRET assays
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| DC21644 | SHP504 Featured |
SHP504 is a distinct, allosteric site 2 SHP2 inhibitor with IC50 of 21 uM (SHP2 1-525), and selective over the phosphatase domain (SHP2 PTP IC50>100 uM).downregulates DUSP6 mRNA, a downstream MAPK pathway marker, in KYSE-520 cancer cells.
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| DC39250 | HCoV-229E Spike Glycoprotein peptide library Featured |
This pool is delivered in subpools of 291 peptides derived from a peptide scan through the entire Spike glycoprotein (Protein ID: P15423) of Human coronavirus 229E (HCoV-229E) for T cell assays. 5mg per peptide, purity>95%
Total Length: 1173 AA; Sequence:
MFVLLVAYAL LHIAGCQTTN GLNTSYSVCN GCVGYSENVF AVESGGYIPS DFAFNNWFLL TNTSSVVDGV
VRSFQPLLLN CLWSVSGLRF TTGFVYFNGT GRGDCKGFSS DVLSDVIRYN LNFEENLRRG TILFKTSYGV
VVFYCTNNTL VSGDAHIPFG TVLGNFYCFV NTTIGNETTS AFVGALPKTV REFVISRTGH FYINGYRYFT
LGNVEAVNFN VTTAETTDFC TVALASYADV LVNVSQTSIA NIIYCNSVIN RLRCDQLSFD VPDGFYSTSP
IQSVELPVSI VSLPVYHKHT FIVLYVDFKP QSGGGKCFNC YPAGVNITLA NFNETKGPLC VDTSHFTTKY
VAVYANVGRW SASINTGNCP FSFGKVNNFV KFGSVCFSLK DIPGGCAMPI VANWAYSKYY TIGSLYVSWS
DGDGITGVPQ PVEGVSSFMN VTLDKCTKYN IYDVSGVGVI RVSNDTFLNG ITYTSTSGNL LGFKDVTKGT
IYSITPCNPP DQLVVYQQAV VGAMLSENFT SYGFSNVVEL PKFFYASNGT YNCTDAVLTY SSFGVCADGS
IIAVQPRNVS YDSVSAIVTA NLSIPSNWTT SVQVEYLQIT STPIVVDCST YVCNGNVRCV ELLKQYTSAC
KTIEDALRNS ARLESADVSE MLTFDKKAFT LANVSSFGDY NLSSVIPSLP TSGSRVAGRS AIEDILFSKL
VTSGLGTVDA DYKKCTKGLS IADLACAQYY NGIMVLPGVA DAERMAMYTG SLIGGIALGG LTSAVSIPFS
LAIQARLNYV ALQTDVLQEN QKILAASFNK AMTNIVDAFT GVNDAITQTS QALQTVATAL NKIQDVVNQQ
GNSLNHLTSQ LRQNFQAISS SIQAIYDRLD TIQADQQVDR LITGRLAALN VFVSHTLTKY TEVRASRQLA
QQKVNECVKS QSKRYGFCGN GTHIFSIVNA APEGLVFLHT VLLPTQYKDV EAWSGLCVDG TNGYVLRQPN
LALYKEGNYY RITSRIMFEP RIPTMADFVQ IENCNVTFVN ISRSELQTIV PEYIDVNKTL QELSYKLPNY
TVPDLVVEQY NQTILNLTSE ISTLENKSAE LNYTVQKLQT LIDNINSTLV DLKWLNRVET YIKWPWWVWL
CISVVLIFVV SMLLLCCCST GCCGFFSCFA SSIRGCCEST KLPYYDVEKI HIQ
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| DC39220 | STING agonist compound 17 Featured |
STING agonist compound 17 is a selective stimulator of interferon genes (STING) receptor agonist.
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| DC3102 | GDC-0879 |
GDC-0879 is a novel potent, selective B-Raf inhibitor for B-RafV600E with IC50 of 0.13 nM.
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| DC10063 | MPI-5a Featured |
MPI_5a is a potent selective inhibitor of HDAC6, and poorly blocks other HDAC enzymes.
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| DC39115 | LCB-1 protein Featured |
LCB-1 is a designed antiviral protein inhibiting SARS-CoV-2. LCB1 is roughly six times more potent on a per mass basis than the most effective monoclonal antibodies reported thus far.LCB1 is currently being evaluated in rodents. LCB1 binds the Spike receptor binding domain (RBD) with affinity below 1 nM and blocks ARS-CoV-2 infection of Vero E6 cells with IC50 of 23.54 pM.
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| DC7491 | RWJ67657 |
RWJ67657 is a selective p38α and p38β inhibitor (IC50 values are 1 and 11 μM respectively) that displays no activity at p38γ, p38δ and a range of other kinases.
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| DC10011 | Centrinone-B |
Centrinone-B is a high affinity and selective PLK4 inhibitor (Ki = 0.59 nM).
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| DC39111 | Tubastatin A TFA |
Tubastatin A TFA (Tubastatin A trifluoroacetate salt) is a potent and selective HDAC6 inhibitor with IC50 of 15 nM in a cell-free assay. It is selective against all the other isozymes (1000-fold) except HDAC8 (57-fold). Tubastatin A promotes autophagy and increases apoptosis.
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| DC39110 | TGF-beta/Smad inhibitor |
The 1D11.16.8 monoclonal antibody reacts with mouse, human, rat, monkey, hamster, canine and bovine TGF-β (transforming growth factor beta) isoforms 1, 2 and 3.The 1D11.16.8 monoclonal antibody is a neutralizing antibody.
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