| DC72690 |
Pteropterin monohydrate |
Pteropterin (Pteroyltriglutamic) monohydrate is an active form of folate. Pteropterin monohydrate shows inhibiting effect on tumor growth and has broad anticancer activity. |
|
| DC72691 |
Fmoc-Asp(OtBu)-CH2COOH |
Fmoc-Asp(OtBu)-CH2COOH is a linker. |
|
| DC72692 |
Cidofovir diphosphate |
Cidofovir diphosphate is an active intracellular metabolite of Cidofovir. Cidofovir diphosphate is a selective inhibitor of viral DNA polymerases with Ki values of 6.6, 0.86 and 1.4 μM for HCMV, HSV-1 and HSV-2 DNA polymerase, respectively. |
|
| DC72693 |
NSC363998 free base |
NSC363998 (free base) is an orally active compound. NSC363998 (free base) can suppress rCGG90 induced neurotoxicity. NSC363998 (free base) can be used for the research of neurodegenerative disorder such as Fragile X associated tremor/ataxia syndrome (FXTAS). |
|
| DC72694 |
5(S)-HETE lactone |
5(S)-HETE lactone is an arachidonic acid (AA) metabolite. |
|
| DC72695 |
(E)-5-Octadecene |
(E)-5-Octadecene ((E)-Octadec-5-ene) is a sex pheromone or a related chemical component. (E)-5-Octadecene has effect on destruction of sexual attraction of female moth of rice borers moth (Chilo suppressalis Walker). |
|
| DC72696 |
YEATS4 binder-1 |
YEATS4 binder-1(4e) is a potent and selective YEATS4 binder that binds to the KAc recognition site of the YEATS structural domain with a Ki value of 37 nM. |
|
| DC72697 |
(S,S)-GNE 5729 |
(S,S)-GNE 5729 is a (S,S)-enantiomer of GNE 5729. |
|
| DC72698 |
L-Allooctopine |
L-Allooctopine is a competitive inhibitor of D-octopine. |
|
| DC72699 |
Compound C108
Featured
|
Compound C108 is a G3BP2 inhibitor. Compound C108 also targeted stress granule-associated proteins and Gtpase-activating protein (SH3 domain) binding protein 2. Compound C108 potently inhibits esophageal squamous cell carcinoma (ESCC) cell metastasis. |
|
| DC72700 |
Oleyl alcohol |
Oleyl alcohol is an active compound. Oleyl alcohol can be used for various studies. |
|
| DC72701 |
mono-Pal-MTO |
mono-Pal-MTO is a palm oil-based lipid produced by combining the anticancer drug mitoxantrone (MTO) with palmitoleic acid. When nanoparticles of mono-Pal-MTO and di-Pal-MTO are combined in a molar ratio of 1:1, they show effective siRNA cell delivery and enhance anticancer activity. |
|
| DC72702 |
Metopimazine |
Metopimazine (EXP999) is a phenothiazine derivative used to prevent emesis during chemotherapy. Metopimazine belongs to the anti-dopaminergic anti-emetics (ADA) class. Metopimazine can be used for the research of gastroenteritis (GE) . |
|
| DC72703 |
Cyprodenate |
Cyprodenate (Actebral) is an orally active psychotonic brain stimulant. Cyprodenate can be used for the research of metabolism. |
|
| DC72704 |
Gal-C4-Chol |
Gal-C4-Chol is a glycosylated cholesterol derivative. Gal-C4-Chol can be used as a ligand for asialoglycoprotein receptors (ASGPR) to prepare Galactosylated (Gal) liposomes. Gal-C4-Chol can be used to prepare simple lipid-based nanoparticles. |
|
| DC72705 |
Pteropterin |
Pteropterin (Pteroyltriglutamic) is an active form of folate. Pteropterin shows inhibiting effect on tumor growth and has broad anticancer activity. |
|
| DC72706 |
Thiocystine |
Thiocystine is a relatively stable trisulfide analog of Cystine. Thiocystine functions as a persullide in transferring its sulfane sulfur to thiophilic acceptors. |
|
| DC72707 |
ASO 556089 |
ASO 556089 is a 16 nucleotide length gap protein (3-10-3) that targets MALAT1, a long non-coding human and mouse RNA. ASO 556089 is an antisense oligonucleotide (ASO) with the sequence 5 '-GmCATTmCTAATAGmCAGmC-3'. |
|
| DC72708 |
di-Pal-MTO |
di-Pal-MTO is a palm oil-based lipid produced by combining the anticancer drug mitoxantrone (MTO) with palmitoleic acid. When nanoparticles of mono-Pal-MTO and di-Pal-MTO are combined in a molar ratio of 1:1, they show effective siRNA cell delivery and enhance anticancer activity. |
.png)
|
| DC72709 |
BMS-593214 |
BMS-593214 is an active site-directed factor (F) VIIa inhibitor. BMS-593214 shows antithrombotic and antihaemostatic properties. BMS-593214 is a direct competitive inhibitor of human FVIIa and a non-competitive inhibitor of Viia-activated substrate FX. BMS-593214 prevents electroinduced carotid artery thrombosis (AT) and wire induced vena cava thrombosis (VT). |
|
| DC72710 |
Osivelotor |
Osivelotor is an allosteric modulator of haemoglobin S (HbS). |
|
| DC72711 |
Polyoxin C |
Polyoxin C, the hybrid compound of nucleosides and R-amino acids, is important as the C-terminal amino acid component of Nikkomycin. |
|
| DC72712 |
Clomacran |
Clomacran (SKF 14336; SKF 14336D) is a potent antipsychotic agent. |
|
| DC72713 |
H-Gly-Oet |
H-Gly-Oet can be coupled with Z-Pro-Leu-OEt for the synthesis of tripeptide Z-Pro-Leu-Gly-OEt by thermolysin and α-chymotrypsin catalysis. |
|
| DC72714 |
Vonifimod |
Vonifimod is an immunomodulator. |
|
| DC72715 |
Picibanil |
Picibanil (OK-432) is a streptococcal preparation with potent biological response modifying activities. Picibanil also has anticancer activity. Picibanil can be used for the research of cancers such as lymphangiomas. |
|
| DC72716 |
BA 41899 |
BA 41899 is a purely calcium-sensitizing agent. BA 41899 is completely devoid of phosphodiesterase (PDE) III inhibitory activity or any other known inotropic mechanism. BA 41899 can be used for the research of cardiovascular diseases, such as congestive heart failure (CHF). |
|
| DC72717 |
PG-11047 |
PG-11047 (CGC-11047) is a polyamine analogue. PG-11047 can be used for the research of breast cancer. |
|
| DC72718 |
S19-1035
Featured
|
S19-1035 is a highly potent and specific aldo-keto reductase 1C3 (AKR1C3) inhibitor. S19-1035 inhibits AKR1C3 with an IC50 value of 3.04 nM. S19-1035 can be used for the research of tumor. |
|
| DC72719 |
BAY-5000 |
BAY-5000 (example 32) is a pyrimidinedione derivative. BAY-5000 can be used in the synthesis of cancer-related reagents. |
|
