Predicted protein targets (top 20)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | LMNA | P02545 | 3/20 | 0.54 |
| ▸ | F2 | P00734 | 1/20 | 0.54 |
| ▸ | PLA2G7 | Q13093 | 2/20 | 0.53 |
| ▸ | TSHR | P16473 | 4/20 | 0.50 |
| ▸ | MAPT | P10636 | 4/20 | 0.45 |
| ▸ | TDP1 | Q9NUW8 | 3/20 | 0.45 |
| ▸ | TP53 | P04637 | 1/20 | 0.45 |
| ▸ | AKR1C1 | Q04828 | 1/20 | 0.45 |
| ▸ | PLIN1 | O60240 | 1/20 | 0.45 |
| ▸ | BCHE | P06276 | 1/20 | 0.45 |
| ▸ | TNFRSF1A | P19438 | 1/20 | 0.45 |
| ▸ | ACHE | P22303 | 1/20 | 0.45 |
| ▸ | MAOB | P27338 | 1/20 | 0.45 |
| ▸ | RECQL | P46063 | 1/20 | 0.45 |
| ▸ | PLIN5 | Q00G26 | 1/20 | 0.45 |
| ▸ | CYP1B1 | Q16678 | 1/20 | 0.45 |
| ▸ | ABHD5 | Q8WTS1 | 1/20 | 0.45 |
| ▸ | KMT2A | Q03164 | 4/20 | 0.44 |
| ▸ | ALDH1A1 | P00352 | 4/20 | 0.44 |
| ▸ | MAPK1 | P28482 | 1/20 | 0.44 |
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 | |
|---|---|---|---|---|
| SCHEMBL2900886 | 0.82 | CYP1A1 (0.56) | LMNAMAPTTDP1CYP1B1KMT2A | |
| SCHEMBL28182671 | 0.79 | LMNA (0.61) | LMNAF2PLA2G7TSHRMAPT | |
| SCHEMBL11229507 | 0.79 | LMNA (0.61) | LMNAF2PLA2G7TSHRMAPT | |
| SCHEMBL10455847 | 0.79 | PLA2G7 (0.53) | LMNAF2PLA2G7TSHRMAPT | |
| SCHEMBL385227 | 0.79 | PLA2G7 (0.53) | LMNAF2PLA2G7TSHRMAPT | |
| SCHEMBL229640 | 0.77 | LMNA (0.58) | LMNAF2PLA2G7TSHRMAPT | |
| Benzene SCHEMBL28103328 | 0.77 | LMNA (0.58) | LMNAF2PLA2G7TSHRMAPT | |
| SCHEMBL9215281 | 0.76 | LMNA (0.56) | LMNAF2PLA2G7TSHRMAPT | |
| SCHEMBL8422588 | 0.76 | LMNA (0.56) | LMNAF2PLA2G7TSHRMAPT | |
| SCHEMBL7773659 | 0.76 | LMNA (0.56) | LMNAF2PLA2G7TSHRMAPT |
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 85 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-114716386-A | Novel exosome inhibitor and preparation method thereof | 北京和理咨询有限公司 | 2022-07-08 | — | — | CN | claimed |
| CN-107847607-A | Aptamer conjugate of paclitaxel or derivative thereof, and preparation method and application thereof | 北京和理咨询有限公司 | 2018-03-27 | — | — | CN | claimed |
| US-9809822-B2 | Triptolide derivatives and preparation method and use thereof | HONG KONG BAPTIST UNIVERSITY (HK) | 2017-11-07 | — | — | US | claimed |
| CN-105121455-B | Novel triptolide derivative and preparation method and application thereof | 香港浸会大学 | 2017-06-16 | — | — | CN | claimed |
| US-20160362691-A1 | TRIPTOLIDE DERIVATIVES AND PREPARATION METHOD AND USE THEREOF | HONG KONG BAPTIST UNIVERSITY (HK) | 2016-12-15 | — | — | US | claimed |
| CN-105121455-A | Novel triptolide derivative and preparation method and application thereof | UNIV HONG KONG BAPTIST | 2015-12-02 | — | — | CN | claimed |
| EP-0513016-A1 | CYCLOALKYL-SUBSTITUTED GLUTARAMIDE DIURETIC AGENTS | Pfizer Limited (GB) | 1992-11-19 | — | — | EP | claimed |
| EP-0342850-B1 | ENANTIOMERIC GLUTARAMIDE DIURETIC AGENTS | Pfizer Limited (GB) | 1992-05-20 | — | — | EP | claimed |
| CN-1015361-B | ENANTIOMERIC GLUTARAMIDE DIURETIC AGENTS | PFIZER (US) | 1992-02-05 | — | — | CN | claimed |
| EP-0274234-B1 | SPIRO-SUBSITUTED GLUTARAMIDE DIURETIC AGENTS | Pfizer Limited (GB) | 1991-09-11 | — | — | EP | claimed |
| US-5030654-A | Glutaramide diuretic agents | PFIZER INC. (US) | 1991-07-09 | — | — | US | claimed |
| CN-1037704-A | The glutaramide diuretic agents of enantiomorph | PFIZER (US) | 1989-12-06 | — | — | CN | claimed |
| EP-0342850-A1 | Enantiomeric glutaramide diuretic agents | Pfizer Limited (GB) | 1989-11-23 | — | — | EP | claimed |
| EP-0274234-A2 | Spiro-subsituted glutaramide diuretic agents | Pfizer Limited (GB) | 1988-07-13 | — | — | EP | claimed |
| CN-116622005-A | Polymer prodrug compound and preparation method thereof, and polymer prodrug micelle and preparation method thereof | 成都普康生物科技有限公司 | 2023-08-22 | — | — | CN | disclosed |
| CN-114716386-A | Novel exosome inhibitor and preparation method thereof | 北京和理咨询有限公司 | 2022-07-08 | — | — | CN | disclosed |
| CN-107847607-B | Aptamer conjugate of paclitaxel or derivative thereof, and preparation method and application thereof | 北京盈科瑞创新医药股份有限公司 | 2020-11-20 | — | — | CN | disclosed |
| US-4443435-A | ANTICARCINOGENS, HYPOTENSIVE AGENTS, HYPERTHYROIDISM | MERCK & CO., INC. (US) | 1984-04-17 | — | — | US | disclosed |
| EP-0046270-A1 | Novel derivatives of bio-affecting phenolic compounds and pharmaceutical composition containing them | INTERx RESEARCH CORPORATION (US) | 1982-02-24 | — | — | EP | disclosed |
| EP-0038541-A1 | Novel prodrugs of biologically active agents containing mercapto groups, process for preparing and therapeutically effective composition containing the same | MERCK & CO. INC. (US) | 1981-10-28 | — | — | EP | disclosed |
Patent text — is the patent's own abstract consistent with the prediction?
For each of this compound's patents that has machine-readable text (1 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-20160362691-A1 | TRIPTOLIDE DERIVATIVES AND PREPARATION METHOD AND USE THEREOF | TPD52L2, TRDMT1, MCTS1 | LMNA 91/4885F2 2649/4885PLA2G7 2898/4885 |
“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.