| DC23056 |
esperamicin A1
Featured
|
Esperamicin A1 is an enediyne antitumor antibiotics of bacterial origin. |
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| DC9440 |
Estropipate
Featured
|
Estropipate is a form of estrogen, used to treat symptoms of menopause, also used to prevent osteoporosis. |
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| DC3162 |
Eszopiclone |
Eszopiclone is a nonbenzodiazepine hypnotic which is slightly effective for insomnia. |
|
| DC7770 |
Etamicastat |
Etamicastat is a novel dopamine β-hydroxylase inhibitor |
|
| DC21003 |
ETC-206
Featured
|
ETC-206 (ETC-1907206) is a novel potent, selective MNK1/2 inhibitor with IC50 of 64/86 nM, inhibits eIF4E phosphorylation inhibition in HeLa cell line with IC50 of 321 nM. |
|
| DC10267 |
Ethosuximide |
Ethosuximide is a succinimide anticonvulsant, used mainly in absence seizures. |
|
| DC12182 |
Ethyl docosa-4,7,10,13,16,19-hexaenoate |
Ethyl cis-4,7,10,13,16,19-Docosahexaenoate, the ethyl ester of Docosahexaenoate (DHA), is enriched in the ethyl ester fraction by the selective alcoholysis of fatty acid ethyl esters originating from tuna oil with lauryl alcohol. |
|
| DC8821 |
Etifoxine Hydrochloride
Featured
|
Etifoxine Hydrochloride is a psychotropic agent with anxiolytic and anticonvulsant activity. Etifoxine Hydrochloride is an activator of GABAA R β2 and GABAA R β3. |
|
| DC9441 |
Etonogestrel |
Etonogestrel is a steroidal progestin used in hormonal contraceptives.
|
|
| DC2102 |
Etoposide 4'-Phosphate |
Etoposide is a semisynthetic derivative of podophyllotoxin, which inhibits DNA synthesis via topoisomerase II inhibition activity. |
|
| DC10239 |
Etoricoxib
Featured
|
Etoricoxib is a new COX-2 selective inhibitor with anti-inflammatory, antipyretic, analgesic, and potential antineoplastic properties. |
|
| DC4234 |
Etravirine |
Etravirine is a non-nucleoside reverse transcriptase inhibitor (NNRTI) of human immunodeficiency virus type 1 (HIV-1). |
|
| DC9884 |
Etretinate |
Etretinate is an oral aromatic retinoid acid which is effective in psoriasis and other dermatological syndromes. |
|
| DC20376 |
Etriciguat |
Etriciguat is a novel potent, selective, orally available soluble guanylate cyclase (sGC) stimulator.. |
|
| DC12061 |
Eurycomanone |
Eurycomanone could increases spermatogenesis by inhibiting the activity of phosphodiesterase and aromatase in steroidogenesis. |
|
| DC9893 |
Evans Blue |
Evans Blue is a potent inhibitor of the uptake of L-glutamate into synaptic vesicles, also an AMPA/kainate receptor antagonist |
|
| DC7987 |
Encenicline hydrochloride (EVP-6124)
Featured
|
Encenicline hydrochloride (EVP-6124 hydrochloride) is a novel partial agonist of α7 neuronal nicotinic acetylcholine receptors (nAChRs). |
|
| DC21005 |
EXEL-0346 |
EXEL-0346 (EXEL0346) is a novel potent, orally active Glucosylceramide synthase (GCS) inhibitor with IC50 of 2 nM. |
|
| DC8260 |
Exemestane(FCE 24304)
Featured
|
Exemestane(FCE 24304) is an aromatase inhibitor, inhibits human placental and rat ovarian aromatase with IC50 of 30 nM and 40 nM, respectively. |
|
| DC22518 |
Exenatide |
Exenatide (Exendin-4) is a 39-aa peptide, highly potent, long-acting glucagon-like peptide-1 receptor (GLP-1) agonist with IC50 of 3.22 nM. |
|
| DC22517 |
Exendin-4 acetate
Featured
|
Exenatide acetate (Exendin-4 acetate) is the acetate of Exenatide, which is highly potent, long-acting glucagon-like peptide-1 receptor (GLP-1) agonist with IC50 of 3.22 nM.. |
|
| DC9532 |
ADH-1 trifluoroacetate
Featured
|
Exherin (ADH-1) trifluoroacetate is a small, cyclic pentapeptide vascular-targeting agent with potential antineoplastic and antiangiogenic activities; selectively and competitively binds to and blocks N-cadherin.
|
|
| DC20377 |
EZH2-IN-3 |
EZH2-IN-3 is a highly selective small molecule inhibitor of EZH2 and EZH1 with IC50 of 21/197/213 nM for wt EZH2/EZH2 Y641N/wt EZH1 respectively. |
|
| DC20379 |
Factor D inhibitor 6 |
Factor D inhibitor 6 is a potent and selective, orally bioavailable inhibitor of Factor D with IC50 of 30 nM. |
|
| DC23545 |
Factor D inhibitor 7 |
Factor D inhibitor 7 is a potent and selective, orally bioavailable inhibitor of Factor D with IC50 of 50 nM. |
|
| DC21899 |
Fadaltran |
Fadaltran is a α2-adrenoreceptor antagonist.. |
|
| DC11329 |
Fadrozole (hydrochloride)
Featured
|
Fadrozole is a non-steroidal aromatase inhibitor (IC50s = 5 and 1.4 nM for human placental and rat ovarian microsomal aromatase, respectively). |
|
| DC21900 |
FAK inhibitor 5 |
FAK inhibitor 5 is the first highly potent, selective irreversible inhibitor of the FAK kinase with IC50 of 0.6 nM. |
|
| DC21650 |
Famitinib |
Famitinib (SHR1020) is a structural analogue of sunitinib, novel and potent multi-targeted RTK inhibitor, including c-Kit, VEGFR2/3, PDGFRβ, FLT-1/3 receptor and c-RET. |
|
| DC10382 |
Farampator
Featured
|
Farampator (CX-691;Org24448) is an AMPA receptor positive modulator. |
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