| DC70962 |
Cannabicitran |
Cannabicitran is a cannabinoid. Cannabicitran can decrease intraocular pressure in rabbits. |
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| DC70966 |
Cyanidin-3-O-arabinoside |
Cyanidin-3-O-arabinoside is a pigment isolated from flowers of Rhododendron cv. Lems Stormcloud. |
|
| DC70969 |
Fluridone |
Fluridone is an inhibitor of abscisic acid (ABA) biosynthesis. Fluridone suppresses the expression of AchnFAR and TF genes and reduces the formation of primary alcohols. |
|
| DC70971 |
LLY-284 |
LLY-284 is the diastereomer of LLY-283 with much less active. LLY-283 is a potent inhibitor of PRMT5. LLY-284 has the potential for the research of cancer diseases. |
|
| DC70973 |
Neoamygdalin |
Neoamygdalin is a compound identified in the different processed bitter almonds. Neoamygdalin has the potential for the research of cough and asthma. |
|
| DC70974 |
Pirifibrate |
Pirifibrate (EL-466) is a hypolipemic substance. Pirifibrate can be used for the research of hyperlipoproteinemias. |
|
| DC70975 |
Pyraflufen-ethyl |
Pyraflufen-ethyl is a phenylpyrazole herbicide for control of annual and perennial broadleaf weeds. |
|
| DC70977 |
TH5427 |
TH5427 is a promising, targeted inhibitor that can be used to further study NUDT5 activity and ADP-ribose metabolism. TH5427, blocks progestin-dependent, PAR-derived nuclear ATP synthesis and subsequent chromatin remodeling, gene regulation and proliferation in breast cancer cells. NUDT5 is recently identified as a rheostat of hormone-dependent gene regulation and proliferation in breast cancer cells. |
|
| DC70978 |
Thalidomide-piperazine hydrochloride |
Thalidomide-piperazine hydrochloride has the potential for the research of leprosy and multiple myeloma. Thalidomide-piperazine hydrochloride used as a tool in developmental biology leads to important discoveries in the biochemical pathways of limb development. |
|
| DC70985 |
(S,S)-BD-AcAc 2 |
(S,S)-BD-AcAc 2 ((S,S)-Ketone Ester) is a (S,S)-enantiomer of BD-AcAc 2. BD-AcAc 2 elevates the AcAc and acetone levels, thereby produces sustained ketosis and significantly delays central nervous system oxygen toxicity (CNS-OT) seizures. |
|
| DC70986 |
11-trans Leukotriene E4 |
11-trans Leukotriene E4 is an isomer of Leukotriene E4 (LTE4). Slow isomerization of the C-11 double bond of LTE4 leads to the formation of 11-trans LTE4. 11-trans Leukotriene E4 is equipotent to LTE4 in contracting guinea pig ileum. |
|
| DC70987 |
13-Hydroxylupanine |
13-Hydroxylupanine (Hydroxylupanine) is the typical alkaloid profile of sweet lupins.13-Hydroxylupanine blocks ganglionic transmission, decreases cardiac contractility and contracts uterine smooth muscle. |
|
| DC70990 |
16-Epiestriol |
16-Epiestriol is a metabolite of the endogenous estrogen estrone with antibacterial and anti-inflammatory effects. |
|
| DC70996 |
4BAB
Featured
|
4BAB (compound 29) is an irreversible glyoxalase I (GLO1) inhibitor. 4BAB has anticancer effects. |
|
| DC70997 |
4-Hydroxyhippuric acid |
4-Hydroxyhippuric acid is a by-product of metabolism of polyphenols and increases the microflora activity related to the refeeding. |
|
| DC70998 |
6-trans-Leukotriene B4 |
6-trans-leukotriene B4 is a neutrophil chemotaxin in the guinea pig dermis. |
|
| DC71001 |
Alendronate sodium |
Alendronate sodium is an orally active nitrogen-containing bisphosphonate. Alendronate sodium potently inhibits bone resorption. Alendronate sodium is used for the research of postmenopausal osteoporosis. |
|
| DC71007 |
Aucuparin |
Aucuparin, a natural product found in Sorbus aucuparia, inhibits pulmonary fibrosis in a bleomycin (BLM)-induced lung fibrosis mouse model. Anti-inflammatory activity. |
|
| DC71009 |
BAY-R 1005 |
BAY-R 1005, an immunoenhancing agent, is a synthetic glycolipid analogue (GLA), which is supposed to modulate antibody synthesis. |
|
| DC71010 |
Bilirubin Conjugate disodium |
Bilirubin Conjugate disodium is a ditaurate derivative of Bilirubin. Bilirubin, a major end product of heme breakdown, is an important constituent of bile. |
|
| DC71017 |
CCW16 |
CCW16 is the covalent ligand for the E3 ubiquitin ligase RNF4. CCW16 can be used in the synthesis of protein degraders. |
|
| DC71020 |
Coumarin hydrazine |
Coumarin hydrazine is a fluorescent chemical probe (λex=420–450/λem=468 nm) to label cellular protein- and lipid-bound carbonyls. |
|
| DC71024 |
Croverin |
Croverin is a diterpenoid compound isolated from the aerial parts of Croton laui. |
|
| DC71025 |
CS12192 |
CS12192 is a compound improving survival and weight gain. CS12192 has the potential for the research of graft-versus-host disease (GVHD) (extracted from the patent CN112773802A). |
|
| DC71026 |
Cussosaponin C |
Cussosaponin C is a compound isolated from Pulsatilla koreana Nakai. |
|
| DC71027 |
Cyclobutyrol |
Cyclobutyrol is a potent choleretic agent. Cyclobutyrol also inhibits biliary lipid secretion. Cyclobutyrol induces choleretic is unrelated to bile acids. CB and bile acids do not compete for the hepatobiliar transport mechanisms |
|
| DC71028 |
DAUDA
Featured
|
DAUDA (11-(dansylamino) undecanoic acid) is an environment-sensitive fluorescent fatty acid analogue. DAUDA alters its intensities and fluorescent emission spectra on entry into binding proteins. DAUDA is used to determine the relative affinity of natural fatty acids for polymorphs of the Schistosoma mansoni Sm14 fatty acid-binding protein. |
|
| DC71031 |
Deschloro Cetirizine dihydrochloride |
Deschloro Cetirizine Dihydrochloride is a Cetirizine impurity. Cetirizine, a second-generation antihistamine and the carboxylated metabolite of hydroxyzine, is a specific, orally active and long-acting histamine H1-receptor antagonist. |
|
| DC71035 |
Emylcamate |
Emylcamate is a potent muscle relaxant. Emylcamate has the potential for the research of neurological diseases. |
|
| DC71037 |
EUK-118 |
EUK-118 is an analog of EUK 8 and EUK 134 with reduced activity. EUK-118 exhibits superoxide dismutase (SOD) mimetic activity. |
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