Predicted protein targets (top 20)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | S100A4 | P26447 | 6/20 | 0.84 |
| ▸ | MEN1 | O00255 | 9/20 | 0.82 |
| ▸ | THRB | P10828 | 9/20 | 0.82 |
| ▸ | KMT2A | Q03164 | 9/20 | 0.82 |
| ▸ | BLM | P54132 | 8/20 | 0.82 |
| ▸ | RECQL | P46063 | 7/20 | 0.82 |
| ▸ | BRCA1 | P38398 | 6/20 | 0.82 |
| ▸ | SMN1; SMN2 | Q16637 | 6/20 | 0.82 |
| ▸ | HIF1A | Q16665 | 6/20 | 0.82 |
| ▸ | MAPT | P10636 | 6/20 | 0.82 |
| ▸ | TDP1 | Q9NUW8 | 6/20 | 0.82 |
| ▸ | CYP3A4 | P08684 | 4/20 | 0.82 |
| ▸ | USP2 | O75604 | 4/20 | 0.82 |
| ▸ | MAPK1 | P28482 | 4/20 | 0.82 |
| ▸ | TOP2A | P11388 | 4/20 | 0.82 |
| ▸ | HTT | P42858 | 4/20 | 0.82 |
| ▸ | CYP1A2 | P05177 | 3/20 | 0.82 |
| ▸ | CHRM1 | P11229 | 3/20 | 0.82 |
| ▸ | TBXA2R | P21731 | 3/20 | 0.82 |
| ▸ | KDM4E | B2RXH2 | 3/20 | 0.82 |
Click a target to see other patent compounds predicted against it — the reverse direction, in place.
Similar compounds — the chemically nearest patent molecules
Nearest neighbours by Morgan-fingerprint cosine across the patent-compound collection, with each neighbour's top predicted target and the predicted targets it shares with this molecule.
| Compound | similarity | top predicted | shared targets | |
|---|---|---|---|---|
| Hydrochloric Acid SCHEMBL5859468 | 0.99 | S100A4 (0.83) | S100A4MEN1THRBKMT2ABLM | |
| SCHEMBL248564 | 0.95 | S100A4 (0.85) | S100A4MEN1THRBKMT2ABLM | |
| SCHEMBL14164316 | 0.94 | S100A4 (0.84) | S100A4MEN1THRBKMT2ABLM | |
| SCHEMBL10968257 | 0.94 | S100A4 (0.84) | S100A4MEN1THRBKMT2ABLM | |
| SCHEMBL27825155 | 0.94 | S100A4 (0.84) | S100A4MEN1THRBKMT2ABLM | |
| SCHEMBL3763974 | 0.94 | S100A4 (0.84) | S100A4MEN1THRBKMT2ABLM | |
| Hydrochloric Acid SCHEMBL331063 | 0.94 | S100A4 (0.84) | S100A4MEN1THRBKMT2ABLM | |
| SCHEMBL13943294 | 0.94 | S100A4 (0.84) | S100A4MEN1THRBKMT2ABLM | |
| SCHEMBL11563422 | 0.94 | S100A4 (0.84) | S100A4MEN1THRBKMT2ABLM | |
| Hydrochloric Acid SCHEMBL28160744 | 0.94 | S100A4 (0.84) | S100A4MEN1THRBKMT2ABLM |
Similarity is cosine over the 2,048-bit Morgan fingerprint (≈ Tanimoto). Identical fingerprints score 1.00.
Patent provenance — the patents this molecule appears in, and who filed them
Claimed or disclosed in 1195 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| EP-4611903-A1 | METHODS OF TREATING NON-HODGKIN LYMPHOMA | TeneoTwo, Inc. (US) | 2025-09-10 | — | — | EP | claimed |
| US-20250011418-A1 | CANCER SPECIFIC PLECTIN-1 SPECIFIC ANTIBODIES AND METHODS OF USE THEREOF | ZIELBIO, INC. | 2025-01-09 | — | — | US | claimed |
| EP-4427810-A2 | METHODS FOR TREATMENT USING ADOPTIVE CELL THERAPY | Juno Therapeutics, Inc. (US) | 2024-09-11 | — | — | EP | claimed |
| CN-118524843-A | Treatment of B cell malignancies | 阿迪塞特治疗公司 | 2024-08-20 | — | — | CN | claimed |
| WO-2024097218-A1 | METHODS OF TREATING NON-HODGKIN LYMPHOMA | TeneoTwo, Inc. (US) | 2024-05-10 | — | — | WO | claimed |
| EP-3886875-B1 | METHODS FOR TREATMENT USING ADOPTIVE CELL THERAPY | JUNO THERAPEUTICS INC (US) | 2024-05-08 | — | — | EP | claimed |
| CN-116322769-A | Methods for treating multiple myeloma | 詹森生物科技公司 | 2023-06-23 | — | — | CN | claimed |
| WO-2022232420-A1 | CERTAIN N-(1-CYANO-2-PHENYLETHYL)-1,4-OXAZEPANE-2-CARBOXAMIDES FOR TREATING CANCER | INSMED INCORPORATED (US) | 2022-11-03 | — | — | WO | claimed |
| US-20220088070-A1 | METHODS FOR TREATMENT USING ADOPTIVE CELL THERAPY | JUNO THERAPEUTICS, INC. (US) | 2022-03-24 | — | — | US | claimed |
| EP-3886875-A2 | METHODS FOR TREATMENT USING ADOPTIVE CELL THERAPY | Juno Therapeutics, Inc. (US) | 2021-10-06 | — | — | EP | claimed |
| CN-101772500-A | Imidazopyrazines as protein kinase inhibitors | SCHERING CORP | 2010-07-07 | — | — | CN | claimed |
| CN-101341166-A | Synthesis of epirubicin from 13-dihydrodaunorubicine | SOLUX CORP (US) | 2009-01-07 | — | — | CN | claimed |
| EP-1963348-A4 | SYNTHESIS OF EPIRUBICIN FROM 13-DIHYDRODAUNORUBICINE | SOLUX CORP (US) | 2008-12-10 | — | — | EP | claimed |
| CN-101262876-A | Method of treating B cell malignancies with TACI-IG fusion molecules | ZYMOGENETICS INC (US) | 2008-09-10 | — | — | CN | claimed |
| EP-1963348-A2 | SYNTHESIS OF EPIRUBICIN FROM 13-DIHYDRODAUNORUBICINE | Solux Corporation (US) | 2008-09-03 | — | — | EP | claimed |
| WO-2007076345-A2 | SYNTHESIS OF EPIRUBICIN FROM 13-DIHYDRODAUNORUBICINE | SOLUX CORPORATION (US) | 2007-07-05 | — | — | WO | claimed |
| US-20070142309-A1 | SYNTHESIS OF EPIRUBICIN FROM 13-DIHYDRODAUNORUBICINE | SYNBIAS PHARMA LTD (UA) | 2007-06-21 | — | — | US | claimed |
| CN-1375332-A | Composition and method for making Akt cancer gene inactivate and activating P38 precell fade-out gene | UNIV TEXAS (US) | 2002-10-23 | — | — | CN | claimed |
| CN-85107562-B | Method for improving solubility of anthracycline glycoside compound in injection solution | 法米塔利亚·卡洛·埃巴公司 | 1988-06-01 | — | — | CN | claimed |
| CN-85107562-A | Contain anthracene nucleus glucosides preparation of drug combination method | — | 1986-07-23 | — | — | CN | claimed |
Patent text — is the patent's own abstract consistent with the prediction?
For each of this compound's patents that has machine-readable text (2 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.
| Patent | Title | Text reads most about | Predicted target · text-rank |
|---|---|---|---|
| US-20070142309-A1 | SYNTHESIS OF EPIRUBICIN FROM 13-DIHYDRODAUNORUBICINE | DUT, HDAC11, NAA15 | S100A4 3770/4885MEN1 4251/4885THRB 3077/4885 |
| US-20220088070-A1 | METHODS FOR TREATMENT USING ADOPTIVE CELL THERAPY | BCL6, BCL3, CD22 | S100A4 1860/4885MEN1 2811/4885THRB 2667/4885 |
“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.