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H530682
YKL-06-061
YKL-06-061 is a potent and selective SIK (salt-inducible kinase) inhibitor. Salt-inducible kinases …
H555130
YKL-06-062
featured
YKL-06-062 is a second-generation SIK inhibitor. YKL 06-062 induces significant pigmentation after …
H562113
YKL-1-116
YKL-1-116 is a potent, selective and covalent inhibitor of CDK7.
H558735
YKL-5-124
featured
YKL-5-124 is a potent and highly selective covalent CDK7 inhibitor which causes arrest at the G1/S t…
H1010503
YKN72818
featured
YKN72818 is a chemical for drug synthesis.
H598664
Yl 704 A1
Yl 704 A1 is a major component of macrolide antibiotic complex YL-704 isolated from Streptomyces pla…
H525690
YL-0919
featured
YL-0919 is a novel 5-HT1A receptor agonist and selective serotonin reuptake inhibitor.
H406591
YL-109
featured
YL-109 has ability to inhibit breast cancer cell growth and invasiveness in vitro and in vivo. YL-10…
H130312
YL5084
YL5084 is an inhibitor of JNK2, displaying higher selectivity over JNK1. YL5084 covalently binds to …
125737
YL93
YL-93 is a MDM2 and MDM4 inhibitor.
H462401
YLF-466D
YLF-466D is a newly developed AMPK activator, which inhibits platelet aggregation.
H1050061
YLN56861
featured
YLN56861 is a chemical for use in drug synthesis. (Pibrentasvir)
H1045035
YLN61968
featured
YLN61968 is a chemical for use i.n drug synthesis
H1035461
YLN76015
featured
YLN76015 is a chemical for drug synthesis (Cobimetinib).
H1035394
YLN82957
featured
YLN82957 is a chemical for drug synthesis (Ceftazidime).
H1035861
YLN86200
featured
YLN86200 is a chemical for drug synthesis (Ertugliflozin).
H565218
YLT-11
YLT-11 is a polo-like kinase 4 (PLK4) inhibitor which inhibits human breast cancer growth via induci…
H562531
YLT192
YLT192 is an orally active and bioavailable inhibitor of VEGFR2 signaling with potent antiangiogenic…
H563045
YLT205
YLT205 is an inducer of apoptosis in human colorectal cells via the mitochondrial apoptosis pathway.…
H341158
YM 11124
YM 11124 is a biochemical.
H341161
YM 11133
YM 11133 is a biochemical.
H558054
YM 114
YM 114 is a 5-HT(3) receptor anatagonist.
H341159
YM 13650
YM 13650 is a biochemical.
H341164
YM 16151-1
YM 16151-1 is a biochemical.
H341167
YM 16457
YM 16457 is a biochemical.
H341165
YM 16638
YM 16638 is a biochemical.
H341168
YM 212
YM 212 is a biochemical.
H532984
YM 218
YM 218 is a novel, potent, nonpeptide vasopressin V1A receptor-selective antagonist.
H341170
YM 22508
YM 22508 is a biochemical.
H341171
YM 26567-1
YM 26567-1 is a biochemical.
H532985
YM 298198 Hydrochloride
YM 298198 Hydrochloride is a non-competitive antagonist with high affinity and selectivity for mGlu1…
H532990
YM 471
YM 471 is an orally active, non-peptide arginine vasopressin (AVP) V1A and V2 receptor antagonist.
H341162
YM 534
YM 534 is a biochemical.
H341155
YM 9429
YM 9429 is a biochemical.
H527470
YM-01 Tosylate
featured
YM-01 Tosylate is a potent antitumor agent, selectively targeting cancer cells and overcoming tamoxi…
H532982
YM-022
featured
YM-022 is a highly potent and selective non-peptide CCK-BR silent antagonist (Ki values are 68 pM an…
H341156
YM-08050
YM-08050 is a biochemical.
H112004
YM-155 Cl
featured
YM-155 is a survivin inhibitor. It inhibits survivin promoter activity in a reporter assay (IC50 = 0…
H121005
YM-1758735
YM-1758735 is an antagonist.
H525383
YM-17690
YM-17690 is a novel non-analogous leukotriene agonist.
H532983
YM-202074
YM-202074 is a high affinity, selective metabotropic glutamate receptor type 1 (mGlu1) antagonist. Y…
H574942
YM-244769 dihydrochloride
YM-244769 dihydrochloride is a Na+/Ca2+ exchange inhibitor (reverse mode). It can also act as a neur…
H565455
YM-254890
featured
YM-254890 is a novel gαq/11-selective inhibitor, inhibiting adp-induced platelet aggregation and blo…
H526945
YM-264 fumarate
YM-264 is a selective, potent and orally active platelet-activating factor antagonist potentially fo…
H574939
YM-26734
featured
YM-26734 is an inhibitor of rabbit platelet sPLA2. YM-26734 has been used to ameliorate local inflam…
H532987
YM-355179
YM-355179 is a novel, selective, and orally available antagonist for CC chemokine receptor 3.
H526924
YM-358 potassium hydrate
YM-358 potassium hydrate is a angiotensin type 1 receptor antagonist potentially for the treatment o…
H526940
YM-430
YM-430, also known as YM-15430; YM-154301; is a dual of β1 adrenergic receptor antagonist and calciu…
H530134
YM-440
YM-440 is an insulin sensitizer potentially for the treatment of type 2 diabetes. Through research, …
H466204
YM-458
YM-458 is a Dual EZH2/BRD4 Inhibitors to Target Solid Tumors. It has an IC50 (EZH2)=490 nM and IC50 …
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