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5-(5-Fluoro-2-oxo-1,2-dihydro-indol-3-ylidenemethyl)-2,4-dimethyl-1H-pyrrole-3-carboxylic Acid is a sunitinib impurity.

Rocepafant (LAU8080) is a platelet-activating factor (PAF) antagonist that attenuates hypoxic-ischemic brain damage in neonatal rats.Rocepafant inhibits tumor necrosis factor-Afa-mediated cytotoxicity in mouse L929 tumor cells.

[1,1'-Bis(diphenylphosphino)ferrocene]dichloropalladium(II) (PDCL2(DPPF)) is a catalyst.

Crocetin β-D-glucopyranoside, an active component of saffron pigments[1].

Erythrocentauric acid is a natural product from Gentiana macrophylla.

Crocetin dialdehyde, a natural product, is present in saffron [1].

Dipyrocetyl has anti-inflammatory and analgesic effects.

Erythrocentaurin has antibacterial activity; it also exhibits a concentration-dependent α-amylase inhibition (IC(50) 1.67 ± 0.28 mg/mL).

Nitrocefin is an antibiotic. It being sensitive to hydrolysis by all lactamases produced by gram-positive and gram-negative bacteria.

C8 Dihydroceramide acts as a negative control for C8 Ceramide, a cell-permeable analog of natural ceramides. C8 Ceramide, also known as N-Octanoyl-D-erythro-sphingosine, exhibits potent chemotherapeutic properties and anti-proliferation effects. Additionally, it stimulates dendritic cells to enhance T cell responses during viral infections. In vitro studies have also shown that C8 Ceramide induces a slight activation of protein kinase (PKC) [4].

(S)-1-[(S)-tert-Butylphosphinoyl]-2-[(S)-1-(diphenylphosphino)ethyl]ferrocene is a useful organic compound for research related to life sciences and the catalog number is T67235.

Procerine is a useful organic compound for research related to life sciences and the catalog number is T124398.

Valrocemide (TV1901), also known as TV-1901, is an antiepileptic drug (AED). Valrocemide has a broad spectrum of anticonvulsant activity and promising potential as a new AED. Valrocemide is an anticonvulsant agent under development by Teva and Acorda as a potential therapeutic for the treatment of epilepsy.

(R)-1-[(R)-1-(Di-tert-butylphosphino)ethyl]-2-[(R)-phenylphosphinoyl]ferrocene is a useful organic compound for research related to life sciences and the catalog number is T67232.

Transcrocetinate disodium (Disodium trans-crocetinate), extracted from saffron (Crocus sativus L.), is a high-affinity antagonist of NMDA receptor.

Tetraethylammonium hexachlorocerate(IV) is a useful organic compound for research related to life sciences and the catalog number is T64591.

Transcrocetin (8,8'-Diapocarotenedioic Acid) is a singlet oxygen quencher.

β-Crocetin is a natural product from Plant

Dihydrocelastrol is synthesized by hydrogenation of celastrol, a treterpene isolated from Chinese medicinal plant Tripterygium regelii. Dihydrocelastrol could inhibit cell proliferation and promote apoptosis through caspase-dependent way in vitro. DHCE co

1,2,3,4,5-Pentaphenyl-1'-(di-tert-butylphosphino)ferrocene is a useful organic compound for research related to life sciences. The catalog number is T65527 and the CAS number is 312959-24-3.

Dihydrocephalomannine is similar to paclitaxel, showing reduced cytotoxicity and tubulin binding.

(S)-1-[(S)-1-(Di-tert-butylphosphino)ethyl]-2-[(S)-phenylphosphinoyl]ferrocene is a useful organic compound for research related to life sciences and the catalog number is T67233.

Crocetin (Transcrocetin) meglumine, sourced from Crocus sativus L. (saffron), functions as a high-affinity antagonist of the NMDA receptor.

(R)-1-[(R)-tert-Butylphosphinoyl]-2-[(R)-1-(diphenylphosphino)ethyl]ferrocene is a useful organic compound for research related to life sciences and the catalog number is T67234.

1-Acetylferrocene, an organoiron compound with the formula Fe, consists of ferrocene substituted by an acetyl group on one of the cyclopentadienyl rings. It is an orange, air-stable solid and is soluble in organic solvents.

Transcrocetin meglumine salt is a natural product isolated from saffron (Crocus sativus L.) and is a high-affinity antagonist of the NMDA receptor.

Crocetine dimethyl ester (Dimethylcrocetin) is a saffronin derivative with antioxidant activity, inhibition of AChE activity, and inhibition of cell growth and differentiation.

Pyr10 is a pyrazole derivative and a selective TRP cation 3 inhibitor. Pyr10 has the ability to distinguish between receptor-operated TRPC3 and native stromal interaction molecule 1 (STIM1)/Orai1 channels. Pyr10 inhibits Ca2+ influx in carbachol-stimulate