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Chemical Structure Cat. No. Product Name CAS No.
Methoxamine hydrochlorid Chemical Structure
BCP19863 Methoxamine hydrochlorid 61-16-5
Methoxamine Hydrochloride is an alpha-1 adrenergic agonist that causes prolonged peripheral vasoconstriction.
Fosphenytoin sodium Chemical Structure
BCP13859 Fosphenytoin sodium 92134-98-0
Fosphenytoin sodium is a phenytoin prodrug with similar anticonvulsant properties.
Maduramycin ammonium Chemical Structure
BCP13419 Maduramycin ammonium 84878-61-5
Maduramicin inhibits proliferation and induces apoptosis in myoblast cells.
Ecamsule Chemical Structure
BCP16962 Ecamsule 92761-26-7
Ecamsule is an organic compound which is added to many sunscreens to filter out UVA rays.
Naloxone hydrochloride dihydrate Chemical Structure
BCP16978 Naloxone hydrochloride dihydrate 51481-60-8
Naloxone HCl Dihydrate is a specific opiate antagonist.
Uniconazole Chemical Structure
BCP13880 Uniconazole 83657-22-1
Uniconazole is a triazole chemical used as a plant growth retardant.
2-Hydrazinoadenosine Chemical Structure
BCP30231 2-Hydrazinoadenosine 15763-11-8
Clopidogrel Besylate Chemical Structure
BCP13469 Clopidogrel Besylate 744256-69-7
Clopidogrel besylate is a ticlopidine analog and platelet purinergic P2Y receptor antagonist that inhibits adenosine diphosphate-mediated PLATELET AGGREGATION.
PD-404182 Chemical Structure
BCP30232 PD-404182 72596-74-8
PD-404182 is an inhibitor of KDO 8-P synthase (Ki = 26 nM).
5-Methylthiophene-2-boronic acid pinacol ester Chemical Structure
BCP30230 5-Methylthiophene-2-boronic acid pinacol ester 476004-80-5
2-(5-Hexylthiophen-2-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane Chemical Structure
BCP30229 2-(5-Hexylthiophen-2-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane 917985-54-7
(S)-(-)-Praziquantel Chemical Structure
BCP30228 (S)-(-)-Praziquantel 57452-97-8
Praziquantel is a highly effective anthelmintic against all Schistosoma species and many cestode infestations.
Trimetazidine Chemical Structure
BCP16534 Trimetazidine 5011-34-7
Trimetazidine is a vasodilator used in angina of effort or ischemic heart disease.
Rp-8-bromo-Cyclic AMPS sodium salt Chemical Structure
BCP29965 Rp-8-bromo-Cyclic AMPS sodium salt 925456-59-3
Rp-8-bromo-Cyclic AMPS (Rp-8-bromo-cAMPS) is a cell-permeable cAMP analog that combines an exocyclic sulfur substitution in the equatorial position of the cyclophosphate ring with a bromine substitution in the adenine base of cAMP.
Z-Phe-Tyr(tBu)-diazomethylketone Chemical Structure
BCP29942 Z-Phe-Tyr(tBu)-diazomethylketone 114014-15-2
Z-Phe-Tyr(tBu)-diazomethylketone is an irreversible cathepsin L inhibitor which is ca 10'000 times more effective in inactivating cathepsin L than cathepsin S.
Telotristat Dibesilate Chemical Structure
BCP29779 Telotristat Dibesilate 1374745-47-7
Telotristat besilate is a tryptophan hydroxylase inhibitor.
AZD-8931 Difumaric acid Chemical Structure
BCP24789 AZD-8931 Difumaric acid 1196531-39-1
AZD-8931 is a reversible, ATP competitive EGFR inhibitor of with IC50s of 4, 3 and 4 nM for EGFR, ErbB2 and ErbB3 in cells, respectively.
Dipivefrin hydrochloride Chemical Structure
BCP13649 Dipivefrin hydrochloride 64019-93-8
Dipivefrin hydrochloride is the hydrochloride salt of dipivefrin. It is used topically as eye drops to reduce intra-ocular pressure in the treatment of open-angle glaucoma or ocular hypertension. It has a role as an adrenergic agonist, a sympathomimetic agent and an antiglaucoma drug. It contains a dipivefrin(1+).
Ranirestat Chemical Structure
BCP14386 Ranirestat 147254-64-6
Ranirestat is an aldose reductase inhibitor being developed for the treatment of diabetic neuropathy.
Rufloxacin hydrochloride Chemical Structure
BCP13481 Rufloxacin hydrochloride 106017-08-7
Rufloxacin hydrochloride is a fluoroquinolone antibacterial, inhibits B-cell differentiation in human mononuclear cells, inhibits Topo.
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