Remission & chronicity
Biomarker Targets & Therapeutic Agents
Gene targets queried against DGIdb, Open Targets, ChEMBL, PubMed, and Europe PMC. Agents ranked: Clinical > Mechanistic > Correlative.
CALCR
| Therapeutic Agent | Effect Direction | Evidence Tier | Potency | Source |
|---|---|---|---|---|
| ADRENOMEDULLIN 2/INTERMEDIN | ↑ activates | Mechanistic | DGIdb | |
| DAVALINTIDE | ↑ activates | Mechanistic | DGIdb | |
| HUMAN CALCITONIN | ↑ activates | Mechanistic | DGIdb | |
| CALCITONIN HUMAN | ↑ activates | Mechanistic | DGIdb | |
| Β-CGRP | ↑ activates | Mechanistic | DGIdb | |
| CALCITONIN | ? unclear | Mechanistic | DGIdb | |
| SALMON CALCITONIN | ↑ activates | Mechanistic | DGIdb | |
| CALCITONIN SALMON | ↑ activates | Mechanistic | DGIdb | |
| Α-CGRP | ↑ activates | Mechanistic | DGIdb | |
| [125I]CALCITONIN | ↑ activates | Mechanistic | DGIdb | |
| CAGRILINTIDE | ↑ activates | Mechanistic | DGIdb | |
| ADRENOMEDULLIN | ↑ activates | Mechanistic | DGIdb | |
| AMYLIN | ↑ activates | Mechanistic | DGIdb | |
| SMC021 | ↑ activates | Mechanistic | DGIdb | |
| PRAMLINTIDE | ↑ activates | Mechanistic | DGIdb | |
| AC187 | ↓ inhibits | Mechanistic | DGIdb | |
| PRAMLINTIDE ACETATE | ↑ activates | Mechanistic | DGIdb | |
| LIPROTAMASE | ? unclear | Mechanistic | DGIdb | |
| [125I]CALCITONIN (SALMON) | ↑ activates | Mechanistic | DGIdb | |
| AMLINTIDE | ↑ activates | Mechanistic | DGIdb | |
| KBP-066 | ↑ activates | Mechanistic | DGIdb | |
| NN1213 | ↑ activates | Mechanistic | DGIdb | |
| CALCITONIN-(8-32) (SALMON) | ↓ inhibits | Mechanistic | DGIdb | |
| KBP-088 | ↑ activates | Mechanistic | DGIdb | |
| CHEMBL2369886 | ↓ inhibits | Mechanistic | 0.069 nM (Ki) | ChEMBL |
| CHEMBL2369897 | ↓ inhibits | Mechanistic | 5.28 nM (Ki) | ChEMBL |
| CHEMBL2369893 | ↓ inhibits | Mechanistic | 0.56 nM (Ki) | ChEMBL |
| CHEMBL2369915 | ↓ inhibits | Mechanistic | 0.069 nM (Ki) | ChEMBL |
| CHEMBL2369895 | ↓ inhibits | Mechanistic | 0.023 nM (Ki) | ChEMBL |
| CHEMBL2304022 | ↓ inhibits | Mechanistic | 1229.0 nM (Ki) | ChEMBL |
| CHEMBL2369899 | ↓ inhibits | Mechanistic | 195.0 nM (Ki) | ChEMBL |
| CHEMBL2369905 | ↓ inhibits | Mechanistic | 400.0 nM (Ki) | ChEMBL |
| CHEMBL2369912 | ↓ inhibits | Mechanistic | 0.05 nM (Ki) | ChEMBL |
| CHEMBL2369892 | ↓ inhibits | Mechanistic | 42.5 nM (Ki) | ChEMBL |
| CHEMBL2369907 | ↓ inhibits | Mechanistic | 0.051 nM (Ki) | ChEMBL |
| CHEMBL2369904 | ↓ inhibits | Mechanistic | 2569.0 nM (Ki) | ChEMBL |
| CHEMBL2035983 | ↓ inhibits | Mechanistic | 3200.0 nM (Ki) | ChEMBL |
| CHEMBL4448157 | ↑ activates | Mechanistic | 0.013 nM (EC50) | ChEMBL |
| CHEMBL4452412 | ↑ activates | Mechanistic | 0.013 nM (EC50) | ChEMBL |
| CHEMBL4457292 | ↑ activates | Mechanistic | 0.017 nM (EC50) | ChEMBL |
Showing top 40 of 141 agents ranked by evidence tier.
CTSK
| Therapeutic Agent | Effect Direction | Evidence Tier | Potency | Source |
|---|---|---|---|---|
| ODANACATIB | ↓ inhibits | Mechanistic | DGIdb | |
| CALPEPTIN | ↓ inhibits | Mechanistic | 0.11 nM (IC50) | DGIdb |
| BALICATIB | ↓ inhibits | Mechanistic | DGIdb | |
| MIV-701 | ? unclear | Mechanistic | DGIdb | |
| RELACATIB | ↓ inhibits | Mechanistic | DGIdb | |
| HEPARAN SULFATE | ? unclear | Mechanistic | DGIdb | |
| ANTISENSE OLIGONUCLEOTIDES | ? unclear | Mechanistic | DGIdb | |
| GC-376 | ↓ inhibits | Mechanistic | DGIdb | |
| UAWJ9-36-3 | ↓ inhibits | Mechanistic | DGIdb | |
| K11777 | ↓ inhibits | Mechanistic | DGIdb | |
| COMPOUND 1B [PMID: 16290936] | ↓ inhibits | Mechanistic | DGIdb | |
| COMPOUND 23 [PMID: 35944849] | ↓ inhibits | Mechanistic | DGIdb | |
| CHEMBL:CHEMBL2316602 | ? unclear | Mechanistic | DGIdb | |
| ONO-5334 | ↓ inhibits | Mechanistic | DGIdb | |
| L873724 | ↓ inhibits | Mechanistic | DGIdb | |
| CHEMBL419772 | ↓ inhibits | Mechanistic | 100.0 nM (IC50) | ChEMBL |
| CHEMBL113761 | ↓ inhibits | Mechanistic | 1630.0 nM (IC50) | ChEMBL |
| CHEMBL115734 | ↓ inhibits | Mechanistic | 5.0 nM (IC50) | ChEMBL |
| CHEMBL3142832 | ↓ inhibits | Mechanistic | 230.0 nM (Ki) | ChEMBL |
| CHEMBL3142835 | ↓ inhibits | Mechanistic | 30500.0 nM (Ki) | ChEMBL |
| CHEMBL100563 | ↓ inhibits | Mechanistic | 2.3 nM (Ki) | ChEMBL |
| CHEMBL99890 | ↓ inhibits | Mechanistic | 1.4 nM (Ki) | ChEMBL |
| CHEMBL314777 | ↓ inhibits | Mechanistic | 1061.0 nM (Ki) | ChEMBL |
| CHEMBL86453 | ↓ inhibits | Mechanistic | 492.0 nM (Ki) | ChEMBL |
| CHEMBL264623 | ↓ inhibits | Mechanistic | 683.0 nM (Ki) | ChEMBL |
| CHEMBL299277 | ↓ inhibits | Mechanistic | 330.0 nM (Ki) | ChEMBL |
| CHEMBL87150 | ↓ inhibits | Mechanistic | 229.0 nM (Ki) | ChEMBL |
| CHEMBL294615 | ↓ inhibits | Mechanistic | 33.0 nM (Ki) | ChEMBL |
| CHEMBL57836 | ↓ inhibits | Mechanistic | 10.0 nM (Ki) | ChEMBL |
| CHEMBL313182 | ↓ inhibits | Mechanistic | 1370.0 nM (Ki) | ChEMBL |
| CHEMBL77665 | ↓ inhibits | Mechanistic | 15.0 nM (Ki) | ChEMBL |
| CHEMBL171998 | ↓ inhibits | Mechanistic | 706.0 nM (Ki) | ChEMBL |
| CHEMBL354439 | ↓ inhibits | Mechanistic | 5.0 nM (Ki) | ChEMBL |
| CHEMBL170962 | ↓ inhibits | Mechanistic | 12.0 nM (Ki) | ChEMBL |
| CHEMBL169560 | ↓ inhibits | Mechanistic | 8.0 nM (Ki) | ChEMBL |
| CHEMBL354132 | ↓ inhibits | Mechanistic | 48.0 nM (Ki) | ChEMBL |
| CHEMBL80508 | ↓ inhibits | Mechanistic | 11.0 nM (Ki) | ChEMBL |
| CHEMBL78288 | ↓ inhibits | Mechanistic | 460.0 nM (IC50) | ChEMBL |
| CHEMBL353725 | ↓ inhibits | Mechanistic | 10.0 nM (Ki) | ChEMBL |
| CHEMBL73908 | ↓ inhibits | Mechanistic | 470.0 nM (IC50) | ChEMBL |
Showing top 40 of 178 agents ranked by evidence tier.
ESR1
| Therapeutic Agent | Effect Direction | Evidence Tier | Potency | Source |
|---|---|---|---|---|
| ESTRONE | ↑ activates | Mechanistic | 480.0 nM (EC50) | DGIdb |
| EVEROLIMUS | ? unclear | Mechanistic | DGIdb | |
| ANASTROZOLE | ? unclear | Mechanistic | DGIdb | |
| SIVIFENE | ? unclear | Mechanistic | DGIdb | |
| ARZOXIFENE | ~ modulates | Mechanistic | DGIdb | |
| ENDOXIFEN | ↓ inhibits | Mechanistic | DGIdb | |
| OSPEMIFENE | ↓ inhibits | Mechanistic | DGIdb | |
| RALOXIFEN | ? unclear | Mechanistic | DGIdb | |
| FULVESTRANT | ↓ inhibits | Mechanistic | 6.0 nM (IC50) | DGIdb |
| INAVOLISIB | ? unclear | Mechanistic | DGIdb | |
| TESTOSTERONE PROPIONATE | ? unclear | Mechanistic | DGIdb | |
| PHENYLMERCURIC ACETATE | ? unclear | Mechanistic | DGIdb | |
| ESTRADIOL CYPIONATE | ↑ activates | Mechanistic | DGIdb | |
| ESTROGEN | ? unclear | Mechanistic | DGIdb | |
| METHOXSALEN | ? unclear | Mechanistic | DGIdb | |
| BORIC ACID | ? unclear | Mechanistic | DGIdb | |
| IMLUNESTRANT | ↓ inhibits | Mechanistic | DGIdb | |
| PROTOAPIGENONE | ? unclear | Mechanistic | DGIdb | |
| CLOMIPHENE CITRATE | ? unclear | Mechanistic | DGIdb | |
| DAUNORUBICIN HYDROCHLORIDE | ? unclear | Mechanistic | DGIdb | |
| NERATINIB | ? unclear | Mechanistic | DGIdb | |
| ALACHLOR | ? unclear | Mechanistic | DGIdb | |
| METHAMPHETAMINE | ? unclear | Mechanistic | DGIdb | |
| OCHRATOXIN A | ? unclear | Mechanistic | DGIdb | |
| CETRIMONIUM BROMIDE | ? unclear | Mechanistic | DGIdb | |
| EXEMESTANE | ? unclear | Mechanistic | DGIdb | |
| GW7647 | ? unclear | Mechanistic | DGIdb | |
| NORGESTREL | ? unclear | Mechanistic | DGIdb | |
| AMCENESTRANT | ↓ inhibits | Mechanistic | DGIdb | |
| LETROZOLE | ? unclear | Mechanistic | DGIdb | |
| PROGESTERONE | ? unclear | Mechanistic | DGIdb | |
| DIETHYLSTILBESTROL | ↑ activates | Mechanistic | 12.0 nM (EC50) | DGIdb |
| ESTRIOL | ↑ activates | Mechanistic | DGIdb | |
| 16Α-HYDROXYESTRONE | ↑ activates | Mechanistic | DGIdb | |
| BRILANESTRANT | ? unclear | Mechanistic | DGIdb | |
| LEVONORGESTREL | ? unclear | Mechanistic | DGIdb | |
| ACOLBIFENE | ? unclear | Mechanistic | DGIdb | |
| PROPYLPYRAZOLETRIOL | ↑ activates | Mechanistic | DGIdb | |
| ESTRADIOL VALERATE | ↑ activates | Mechanistic | DGIdb | |
| MEGESTROL | ? unclear | Mechanistic | DGIdb |
Showing top 40 of 386 agents ranked by evidence tier.
LRP5
Pipeline results not yet available for this target. Run the pipeline to populate.
PTH1R
| Therapeutic Agent | Effect Direction | Evidence Tier | Potency | Source |
|---|---|---|---|---|
| PARATHYROID HORMONE | ? unclear | Mechanistic | DGIdb | |
| 9-AMINOCAMPTOTHECIN | ? unclear | Mechanistic | DGIdb | |
| PCO-371 | ↑ activates | Mechanistic | 4100.0 nM (EC50) | DGIdb |
| [ILE5,TRP23]PTHRP-(3-36) (HUMAN) | ↑ activates | Mechanistic | DGIdb | |
| [ALA1,12,AIB3,GLN10,HARG11,TRP14,ARG19]PTH-(1-21)-NH2 (HUMAN) | ↑ activates | Mechanistic | DGIdb | |
| PTHRP-(1-36) | ↑ activates | Mechanistic | DGIdb | |
| [TRP23,TYR36]PTHRP-(1-36)-NH2 (HUMAN) | ↑ activates | Mechanistic | DGIdb | |
| RECOMBINANT PARATHYROID HORMONE-RELATED PROTEIN | ? unclear | Mechanistic | DGIdb | |
| PTHRP-(1-21)/PTH-(22-34) (HUMAN) | ↑ activates | Mechanistic | DGIdb | |
| [ILE5,TRP23]PTHRP-(1-36) (HUMAN) | ↑ activates | Mechanistic | DGIdb | |
| CHEMBL:CHEMBL586870 | ? unclear | Mechanistic | DGIdb | |
| [ALA1,12,AIB3,GLN10,HARG11,TRP14,ARG19]PTH-(1-28)-NH2 (HUMAN) | ↑ activates | Mechanistic | DGIdb | |
| PTH-(1-34) (RAT) | ↑ activates | Mechanistic | DGIdb | |
| [PHE23]PTH-(1-34) (HUMAN) | ↑ activates | Mechanistic | DGIdb | |
| TIP39-(3-39) (HUMAN/BOVINE) | ↓ inhibits | Mechanistic | DGIdb | |
| [HIS5]PTH-(1-34) (HUMAN) | ↑ activates | Mechanistic | DGIdb | |
| CHEMBL:CHEMBL599896 | ? unclear | Mechanistic | DGIdb | |
| [TYR36]-PTHRP-(1-36) AMIDE (HUMAN) | ↑ activates | Mechanistic | DGIdb | |
| TERIPARATIDE ACETATE | ↑ activates | Mechanistic | DGIdb | |
| PTHRP-(1-20)/TIP-(23-39) (HUMAN) | ↑ activates | Mechanistic | DGIdb | |
| [ILE5,TRP23]PTHRP-(4-36) (HUMAN) | ↑ activates | Mechanistic | DGIdb | |
| [TYR34]PTH-(1-34) (HUMAN) | ↑ activates | Mechanistic | DGIdb | |
| DEXAMETHASONE | ? unclear | Mechanistic | DGIdb | |
| [ALA1,12,AIB3,GLN10,HARG11,TRP14]PTH-(1-14)-NH2 | ↑ activates | Mechanistic | DGIdb | |
| ABALOPARATIDE | ↑ activates | Mechanistic | 0.02 nM (EC50) | DGIdb |
| TIP39 | ↓ inhibits | Mechanistic | DGIdb | |
| TIP39-(9-39) (HUMAN/BOVINE) | ↓ inhibits | Mechanistic | DGIdb | |
| [ALA1,12,AIB3,GLN10,HARG11,TRP14,ARG19]PTH-(1-34)-NH2 | ↑ activates | Mechanistic | DGIdb | |
| [ILE5,TRP23,TYR36]PTHRP-(1-36)-NH2 (HUMAN) | ↑ activates | Mechanistic | DGIdb | |
| [125I][NLE8,21,TYR34]PTH-(1-34)-NH2 (RAT) | ↑ activates | Mechanistic | DGIdb | |
| [TRP23]PTHRP-(1-36) (HUMAN) | ↑ activates | Mechanistic | DGIdb | |
| ENEBOPARATIDE | ↑ activates | Mechanistic | DGIdb | |
| [ILE5,TRP23]PTHRP-(2-36) (HUMAN) | ↑ activates | Mechanistic | DGIdb | |
| RECOMBINANT TRANSFORMING GROWTH FACTOR | ? unclear | Mechanistic | DGIdb | |
| OSTABOLIN-C | ? unclear | Mechanistic | DGIdb | |
| [ILE5,TRP23]PTHRP-(5-36) | ↓ inhibits | Mechanistic | DGIdb | |
| DS69910557 | ↓ inhibits | Mechanistic | DGIdb | |
| [D-TRP12,TYR34]PTH-(7-34) (BOVINE) | ↓ inhibits | Mechanistic | DGIdb | |
| PTHRP-(7-34) (HUMAN, RAT, MOUSE) | ↓ inhibits | Mechanistic | DGIdb | |
| TIP39-(7-39) (HUMAN/BOVINE) | ↓ inhibits | Mechanistic | DGIdb |
Showing top 40 of 183 agents ranked by evidence tier.
SOST
| Therapeutic Agent | Effect Direction | Evidence Tier | Potency | Source |
|---|---|---|---|---|
| AMG-167 | ↓ inhibits | Mechanistic | DGIdb | |
| ANTI-SCLEROSTIN | ↓ inhibits | Mechanistic | DGIdb | |
| BLOSOZUMAB | ↓ inhibits | Mechanistic | DGIdb | |
| SETRUSUMAB | ↓ inhibits | Mechanistic | DGIdb | |
| ROMOSOZUMAB | ↓ inhibits | Mechanistic | DGIdb | |
| ALENDRONATE SODIUM | ? unclear | Mechanistic | DGIdb | |
| CHEMBL4454661 | ↑ activates | Mechanistic | 88.3 nM (EC50) | ChEMBL |
| CHEMBL4458856 | ↑ activates | Mechanistic | 156.7 nM (EC50) | ChEMBL |
| CHEMBL4570369 | ↑ activates | Mechanistic | 52.7 nM (EC50) | ChEMBL |
| CHEMBL4546624 | ↑ activates | Mechanistic | 34.2 nM (EC50) | ChEMBL |
| CHEMBL4462045 | ↑ activates | Mechanistic | 162.3 nM (EC50) | ChEMBL |
| CHEMBL4554919 | ↑ activates | Mechanistic | 60.7 nM (EC50) | ChEMBL |
| CHEMBL4573551 | ↑ activates | Mechanistic | 104.0 nM (EC50) | ChEMBL |
| CHEMBL4450022 | ↑ activates | Mechanistic | 802.0 nM (EC50) | ChEMBL |
| CHEMBL4545471 | ↑ activates | Mechanistic | 861.0 nM (EC50) | ChEMBL |
| CHEMBL4456989 | ↑ activates | Mechanistic | 529.0 nM (EC50) | ChEMBL |
| CHEMBL4444758 | ↑ activates | Mechanistic | 1620.0 nM (EC50) | ChEMBL |
| CHEMBL4448674 | ↓ inhibits | Mechanistic | 20.0 nM (IC50) | ChEMBL |
| CHEMBL4475291 | ↓ inhibits | Mechanistic | 20.0 nM (IC50) | ChEMBL |
| CHEMBL4455231 | ↓ inhibits | Mechanistic | 20.0 nM (IC50) | ChEMBL |
| CHEMBL4544777 | ↓ inhibits | Mechanistic | 20.0 nM (IC50) | ChEMBL |
| CHEMBL4459781 | ↓ inhibits | Mechanistic | 20.0 nM (IC50) | ChEMBL |
| CHEMBL4448063 | ↓ inhibits | Mechanistic | 20.0 nM (IC50) | ChEMBL |
| CHEMBL4462260 | ↓ inhibits | Mechanistic | 1500.0 nM (IC50) | ChEMBL |
| OCOTEINE | ↓ inhibits | Mechanistic | 1500.0 nM (IC50) | ChEMBL |
| CHEMBL1560685 | ↓ inhibits | Mechanistic | 1500.0 nM (IC50) | ChEMBL |
| CHEMBL4465758 | ↓ inhibits | Mechanistic | 15000.0 nM (IC50) | ChEMBL |
| CHEMBL464955 | ↓ inhibits | Mechanistic | 1500.0 nM (IC50) | ChEMBL |
| BOLDINE | ↓ inhibits | Mechanistic | 5000.0 nM (IC50) | ChEMBL |
| CHEMBL2021342 | ↓ inhibits | Mechanistic | 37.66 nM (Kd) | ChEMBL |
| CHEMBL5531992 | ↓ inhibits | Mechanistic | 233.7 nM (Kd) | ChEMBL |
| (+)-EPITAXIFOLIN | ↓ inhibits | Mechanistic | 2632.0 nM (Kd) | ChEMBL |
| COUMARIN | ↓ inhibits | Mechanistic | 273.3 nM (Kd) | ChEMBL |
| CHEMBL5531959 | ↓ inhibits | Mechanistic | 397.1 nM (Kd) | ChEMBL |
| CHEMBL5559172 | ↓ inhibits | Mechanistic | 4782.0 nM (Kd) | ChEMBL |
| CIANIDANOL | ↓ inhibits | Mechanistic | 1579.0 nM (Kd) | ChEMBL |
| CHEMBL455364 | ↓ inhibits | Mechanistic | 211.2 nM (Kd) | ChEMBL |
| CHEMBL5558704 | ↓ inhibits | Mechanistic | 19.6 nM (Kd) | ChEMBL |
TNFSF11
| Therapeutic Agent | Effect Direction | Evidence Tier | Potency | Source |
|---|---|---|---|---|
| DENOSUMAB | ↓ inhibits | Mechanistic | DGIdb | |
| LENALIDOMIDE | ? unclear | Mechanistic | DGIdb | |
| CHEMBL4165601 | ↓ inhibits | Mechanistic | 2750.0 nM (Kd) | ChEMBL |
| CHEMBL4161101 | ↓ inhibits | Mechanistic | 4540.0 nM (Kd) | ChEMBL |
| CHEMBL4172400 | ↓ inhibits | Mechanistic | 30910.0 nM (Kd) | ChEMBL |
| CHEMBL4462272 | ↓ inhibits | Mechanistic | 17300.0 nM (Kd) | ChEMBL |
| CHEMBL4457006 | ↓ inhibits | Mechanistic | 614.0 nM (Kd) | ChEMBL |
| CHEMBL4454307 | ↓ inhibits | Mechanistic | 3500.0 nM (Kd) | ChEMBL |
| CHEMBL4554653 | ↓ inhibits | Mechanistic | 3100.0 nM (Kd) | ChEMBL |
| CHEMBL4560856 | ↓ inhibits | Mechanistic | 2700.0 nM (Kd) | ChEMBL |
| CHEMBL1978769 | ↓ inhibits | Mechanistic | 9800.0 nM (Kd) | ChEMBL |
| CHEMBL4436581 | ↓ inhibits | Mechanistic | 13800.0 nM (Kd) | ChEMBL |
| CHEMBL4514088 | ↓ inhibits | Mechanistic | 6300.0 nM (Kd) | ChEMBL |
| CHEMBL4470163 | ↓ inhibits | Mechanistic | 7300.0 nM (Kd) | ChEMBL |
| CHEMBL255489 | ↓ inhibits | Mechanistic | 1000.0 nM (IC50) | ChEMBL |
| CHEMBL4756975 | ↓ inhibits | Mechanistic | 2500.0 nM (IC50) | ChEMBL |
| CHEMBL3742191 | ↓ inhibits | Mechanistic | 1880.0 nM (IC50) | ChEMBL |
| CHEMBL3741720 | ↓ inhibits | Mechanistic | 2860.0 nM (IC50) | ChEMBL |
| CHEMBL3741275 | ↓ inhibits | Mechanistic | 5070.0 nM (IC50) | ChEMBL |
| CHEMBL4745590 | ↓ inhibits | Mechanistic | 2700.0 nM (IC50) | ChEMBL |
| CHEMBL4750116 | ↓ inhibits | Mechanistic | 2000.0 nM (IC50) | ChEMBL |
| CHEMBL4797434 | ↓ inhibits | Mechanistic | 1900.0 nM (IC50) | ChEMBL |
| CHEMBL4760595 | ↓ inhibits | Mechanistic | 1400.0 nM (IC50) | ChEMBL |
| CHEMBL4752672 | ↓ inhibits | Mechanistic | 5100.0 nM (IC50) | ChEMBL |
| CHEMBL4745373 | ↓ inhibits | Mechanistic | 6400.0 nM (IC50) | ChEMBL |
| CHEMBL4794699 | ↓ inhibits | Mechanistic | 8710.0 nM (Kd) | ChEMBL |
| CHEMBL4787527 | ↓ inhibits | Mechanistic | 4900.0 nM (Kd) | ChEMBL |
| CHEMBL4783826 | ↓ inhibits | Mechanistic | 6620.0 nM (Kd) | ChEMBL |
| CHEMBL3741778 | ↓ inhibits | Mechanistic | 4600.0 nM (Kd) | ChEMBL |
| CHEMBL3740423 | ↓ inhibits | Mechanistic | 17610.0 nM (Kd) | ChEMBL |
| CHEMBL3740948 | ↓ inhibits | Mechanistic | 19060.0 nM (Kd) | ChEMBL |
| CHEMBL3740702 | ↓ inhibits | Mechanistic | 11040.0 nM (Kd) | ChEMBL |
| CHEMBL3740051 | ↓ inhibits | Mechanistic | 22300.0 nM (Kd) | ChEMBL |
| CHEMBL3741922 | ↓ inhibits | Mechanistic | 3550.0 nM (Kd) | ChEMBL |
| CHEMBL3740630 | ↓ inhibits | Mechanistic | 12500.0 nM (Kd) | ChEMBL |
| CHEMBL3742150 | ↓ inhibits | Mechanistic | 2820.0 nM (Kd) | ChEMBL |
| CHEMBL3741278 | ↓ inhibits | Mechanistic | 9310.0 nM (Kd) | ChEMBL |
| CHEMBL3741437 | ↓ inhibits | Mechanistic | 5340.0 nM (Kd) | ChEMBL |
| CHEMBL3741883 | ↓ inhibits | Mechanistic | 8490.0 nM (Kd) | ChEMBL |
| CHEMBL3741027 | ↓ inhibits | Mechanistic | 18640.0 nM (Kd) | ChEMBL |
Showing top 40 of 46 agents ranked by evidence tier.
| Therapeutic Agent | Effect Direction | Evidence Tier | Potency | Source |
|---|---|---|---|---|
| PARICALCITOL | ↑ activates | Mechanistic | DGIdb | |
| THIOTEPA | ? unclear | Mechanistic | DGIdb | |
| HEMATOXYLIN | ? unclear | Mechanistic | DGIdb | |
| SLAZINIC ACID | ? unclear | Mechanistic | DGIdb | |
| GOLIMUMAB | ? unclear | Mechanistic | DGIdb | |
| GW5074 | ? unclear | Mechanistic | DGIdb | |
| EPALRESTAT | ? unclear | Mechanistic | DGIdb | |
| 4'-METHOXYCHALCONE | ? unclear | Mechanistic | DGIdb | |
| DESERPIDINE | ? unclear | Mechanistic | DGIdb | |
| BRONOPOL | ? unclear | Mechanistic | DGIdb | |
| CHEMBL:CHEMBL515505 | ? unclear | Mechanistic | DGIdb | |
| RITANSERIN | ? unclear | Mechanistic | DGIdb | |
| RECOMBINANT INTERFERON | ? unclear | Mechanistic | DGIdb | |
| FLUAZINAM | ? unclear | Mechanistic | DGIdb | |
| CALPHOSTIN C | ? unclear | Mechanistic | DGIdb | |
| GALLIC ACID | ? unclear | Mechanistic | DGIdb | |
| TBBT | ? unclear | Mechanistic | DGIdb | |
| FUMARPROTOCETRARIC ACID | ? unclear | Mechanistic | DGIdb | |
| ZAFIRLUKAST | ? unclear | Mechanistic | DGIdb | |
| ZAPA | ? unclear | Mechanistic | DGIdb | |
| SANGUINARINE SULFATE | ? unclear | Mechanistic | DGIdb | |
| IPA-3 | ? unclear | Mechanistic | DGIdb | |
| AGROCLAVINE | ? unclear | Mechanistic | DGIdb | |
| MEDROXYPROGESTERONE | ? unclear | Mechanistic | DGIdb | |
| NISOLDIPINE | ? unclear | Mechanistic | DGIdb | |
| MECYSTEINE HYDROCHLORIDE | ? unclear | Mechanistic | DGIdb | |
| VALSPODAR | ? unclear | Mechanistic | DGIdb | |
| CHEMBL:CHEMBL126804 | ? unclear | Mechanistic | DGIdb | |
| ERYTHROSINE | ? unclear | Mechanistic | DGIdb | |
| SODIUM DODECYL SULFATE | ? unclear | Mechanistic | DGIdb | |
| RT3 | ? unclear | Mechanistic | DGIdb | |
| AMBAZONE | ? unclear | Mechanistic | DGIdb | |
| KEPONE | ? unclear | Mechanistic | DGIdb | |
| CHOLECALCIFEROL | ↑ activates | Mechanistic | DGIdb | |
| S(+)-APOMORPHINE | ? unclear | Mechanistic | DGIdb | |
| PD-118057 | ? unclear | Mechanistic | DGIdb | |
| ETHACRIDINE | ? unclear | Mechanistic | DGIdb | |
| AG 9 | ? unclear | Mechanistic | DGIdb | |
| CALCITRIOL | ↑ activates | Mechanistic | 0.065 nM (Kd) | DGIdb |
| EICOSAPENTAENOIC ACID | ? unclear | Mechanistic | DGIdb |
Showing top 40 of 638 agents ranked by evidence tier.
Clinical Trials
Drug, biologic and supplement trials (treatment or prevention) from ClinicalTrials.gov whose main condition is Osteoporosis: recruiting, active or completed, most recently updated first. Data retrieved 2026-10-28.
This randomised clinical trial aims to study osteoporosis as a disease of accelerated skeletal aging caused by the accumulation of senescent cells within the skeleton and investigate the effects and safety of senolytics and antioxidant therapy on bone.
The primary objective of this study is to characterize safety and tolerability of romosozumab in postmenopausal women with osteoporosis and a high risk of fracture in India.
Previous studies have shown that there is a large inter-individual variability in the degree of bone loss during glucocorticoid treatment, and while some patients experience extensive bone loss other patients\' bone mass remains stable. The aim of the study is to find a biomarker that can be use...
The goal of this randomized-controlled trial is to compare the effect of rhythmic estrogen treatment to continuous estrogen treatment on bone turnover in healthy postmenopausal women. The main question it aims to answer are: • Does rhythmic estrogen lead to increased bone formation in healthy postme...
This randomized open label clinical trial will evaluate the effect of continued denosumab alone over 18 months versus denosumab with added abaloparatide for 18 months. 70 postmenopausal women will be enrolled over a period of 18 months. The co-primary outcomes will be group differences in bone miner...
In this research study the study investigators want to learn more about the effect of two different FDA-approved medication regimens in the treatment of postmenopausal osteoporosis.
Post-menopausal osteoporosis and the resulting fractures are an important cause of disability and loss of independence. They also increase the risk of morbidity and mortality. Given potential side effects, hormone replacement therapy is no longer recommended for menopausal women with risk of becomin...
The purpose of the study is to evaluate the effect of treatment with romosozumab for 6 months compared with placebo on the percent changes in bone mineral density (BMD) at the lumbar spine, at the total hip and femoral neck in postmenopausal Chinese women with osteoporosis.
Our goal is to demonstrate efficacy of the novel agent Denosumab to improve or preserve muscle health, strength, mobility and function in frail older adults.
People with Alzheimer's disease are at an increased risk of bone fracture. Some studies have shown that those taking donepezil have a lower rate of bone fractures, but the reasons for this are unknown. The purpose of this study is to measure the effect of donepezil treatment on bone metabolism facto...
Osteoporotic fractures are a key health problem in older men. Although there are drugs approved to treat osteoporosis in men \[bisphosphonates, denosumab, and teriparatide (TPTD) or PTH(1-34)\], there is a lack of knowledge on how to use them effectively. TPTD is a potent bone anabolic drug, meaning...
This study is a prospective, multicenter, open-label, randomized non-inferiority trial comparing intravenous ibandronate and zoledronic acid as sequential therapy after denosumab discontinuation in postmenopausal women with osteoporosis. This trial primarily targets patients with short-term denosuma...
This study investigates the use of blood tests known as Bone Turnover Markers (BTMs) to quickly monitor the effectiveness of osteoporosis treatment in postmenopausal women. Osteoporosis, which weakens bones and increases fracture risk, is typically monitored using a DEXA scan to measure bone density...
This study is a multicenter, randomized, double-blinded, parallel-group Phase III clinical study to compare the clinical efficacy, safety, and immunogenicity of 9MW0311 and Prolia® in Chinese postmenopausal women with osteoporosis at high risk for fracture.
The goal of this clinical trial is to evaluate the effects of blackcurrant (BC) supplementation on changes in bone density and gut microbiome composition in postmenopausal females.
Agents Found By Disease-Level Search
Searched directly from “Osteoporosis” via ClinicalTrials.gov interventions and Open Targets' disease→drug data — independent of the 8-gene target panel above. This surfaces agents whose mechanism doesn't route through a curated gene (combination therapies, standard-of-care drugs, targets outside the panel).
47 agents shown (approved or with trial evidence) — 42 not found by the gene-target search above.
Teriparatide
Zoledronic AcidNOT in gene-target list
AlendronateNOT in gene-target list
Romosozumab
ZoledronateNOT in gene-target list
Parathyroid Hormone (1-34)NOT in gene-target list
Raloxifene
IbandronateNOT in gene-target list
Parathyroid hormone related protein (1-36)NOT in gene-target list
Soy isoflavonesNOT in gene-target list
BONISTEIN(R) bone blendNOT in gene-target list
Dietary intervention of eating two mealsNOT in gene-target list
Aspara-CA 600 mgNOT in gene-target list
Alfarol 1.0 µgNOT in gene-target list
antiresorptivesNOT in gene-target list
E2/DRSP (Angeliq, BAY86-4891)NOT in gene-target list
Dietary PhytoestrogensNOT in gene-target list
creatine monohydrateNOT in gene-target list
blosozumab (LY2541546)NOT in gene-target list
Shock Wave therapyNOT in gene-target list
bone densitometric examination using REMS technologyNOT in gene-target list
Vit DNOT in gene-target list
PamidronateNOT in gene-target list
ronacaleret (SB-751689)NOT in gene-target list
Balloon KyphoplastyNOT in gene-target list
Vitamin D3NOT in gene-target list
MultivitaminNOT in gene-target list
EchoStation Implementing REMS TechnologyNOT in gene-target list
Atenolol 50 MGNOT in gene-target list
Ground Reaction ForcesNOT in gene-target list
Joint Reaction ForcesNOT in gene-target list
MK0217, /Duration of Treatment : 12 MonthsNOT in gene-target list
Comparator : raloxifene hydrochloride /Duration of Treatment : 12 MonthsNOT in gene-target list
SB-751689 oral tablets (400 mg)NOT in gene-target list
N-Telopeptide, Bone MarkerNOT in gene-target list
Vitamin SupplementsNOT in gene-target list
Calcium supplementNOT in gene-target list
ONO-5920 / YM529NOT in gene-target list
Culinary Medicine InterventionNOT in gene-target list
Whey protein supplementNOT in gene-target list
Calcium and Vitamin D SupplementationNOT in gene-target list
Vitality and biological activity of peripheral blood mononuclear cells (PBMCs)NOT in gene-target list
letrozole
Denosumab InjectionNOT in gene-target list
Abaloparatide
romosozumab HCP administration with PFSNOT in gene-target list
romosozumab self-administration with AI/PenNOT in gene-target list
Generated by the Open Source Medicine Foundation Biomarker Pipeline — 2026-10-08. Data sources: DGIdb, Open Targets, ChEMBL, PubMed, ClinicalTrials.gov. Not medical advice.