Predicted protein targets (top 20)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | L3MBTL1 | Q9Y468 | 2/20 | 0.50 |
| ▸ | MAPT | P10636 | 2/20 | 0.43 |
| ▸ | CYP1A2 | P05177 | 1/20 | 0.43 |
| ▸ | CYP3A4 | P08684 | 1/20 | 0.43 |
| ▸ | CYP2C9 | P11712 | 1/20 | 0.43 |
| ▸ | CYP2C19 | P33261 | 1/20 | 0.43 |
| ▸ | NPSR1 | Q6W5P4 | 1/20 | 0.43 |
| ▸ | ACHE | P22303 | 1/20 | 0.43 |
| ▸ | MEN1 | O00255 | 2/20 | 0.43 |
| ▸ | KMT2A | Q03164 | 2/20 | 0.43 |
| ▸ | SMN1; SMN2 | Q16637 | 1/20 | 0.43 |
| ▸ | NPC1 | O15118 | 1/20 | 0.43 |
| ▸ | RAB9A | P51151 | 1/20 | 0.43 |
| ▸ | HPGD | P15428 | 2/20 | 0.42 |
| ▸ | MRGPRX4 | Q96LA9 | 1/20 | 0.42 |
| ▸ | LMNA | P02545 | 2/20 | 0.41 |
| ▸ | GAA | P10253 | 1/20 | 0.41 |
| ▸ | TP53 | P04637 | 1/20 | 0.40 |
| ▸ | TDP1 | Q9NUW8 | 1/20 | 0.40 |
| ▸ | KDM4E | B2RXH2 | 1/20 | 0.40 |
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 | |
|---|---|---|---|---|
| SCHEMBL29669768 | 1.00 | L3MBTL1 (0.50) | L3MBTL1MAPTCYP1A2CYP3A4CYP2C9 | |
| SCHEMBL21551484 | 0.85 | L3MBTL1 (0.48) | L3MBTL1MAPTCYP1A2CYP3A4CYP2C9 | |
| SCHEMBL11471602 | 0.84 | TSHR (0.50) | MAPTCYP1A2CYP2C9ACHEMEN1 | |
| SCHEMBL37754 | 0.83 | L3MBTL1 (0.53) | L3MBTL1MAPTCYP1A2CYP3A4CYP2C9 | |
| SCHEMBL3371911 | 0.82 | TRPA1 (0.45) | CYP3A4ACHEMEN1KMT2ANPC1 | |
| SCHEMBL2191597 | 0.82 | PDE10A (0.45) | L3MBTL1MAPTCYP1A2CYP3A4CYP2C9 | |
| SCHEMBL982573 | 0.82 | L3MBTL1 (0.51) | L3MBTL1MAPTCYP1A2CYP3A4CYP2C9 | |
| SCHEMBL1799618 | 0.82 | LMNA (0.52) | L3MBTL1MAPTCYP1A2CYP3A4CYP2C9 | |
| SCHEMBL6404163 | 0.82 | L3MBTL1 (0.51) | L3MBTL1MAPTCYP1A2CYP3A4CYP2C9 | |
| SCHEMBL28989055 | 0.81 | ABL1 (0.56) | L3MBTL1MAPTCYP1A2CYP2C19ACHE |
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 76 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-104359990-B | A kind of analyzing detecting method of (S) or (R)-4-chloro-3-hydroxyl butyronitrile | 浙江海正药业股份有限公司 | 2016-09-07 | — | — | CN | claimed |
| CN-102297905-A | HPLC (High Performance Liquid Chromatography) method for utilizing chiral column to separate, identify and prepare monomer matter from cucurbitacin mixture | — | 2011-12-28 | — | — | CN | claimed |
| CN-114751920-A | Antitumor compounds | 法马马有限公司 | 2022-07-15 | — | — | CN | disclosed |
| CN-114736219-A | Antitumor compounds | 法马马有限公司 | 2022-07-12 | — | — | CN | disclosed |
| CN-107207700-B | Method for synthesizing polyoxazolidone compound with high stability | 科思创德国股份有限公司 | 2021-04-27 | — | — | CN | disclosed |
| CN-111004179-B | Resolution method of 5' -methoxylapatin | 武汉大安制药有限公司 | 2021-03-09 | — | — | CN | disclosed |
| CN-111004179-A | Resolution method of 5' -methoxylapatin | 武汉大安制药有限公司 | 2020-04-14 | — | — | CN | disclosed |
| CN-110621678-A | Antitumor compounds | 法马马有限公司 | 2019-12-27 | — | — | CN | disclosed |
| EP-2543736-B1 | METHOD FOR PRODUCING 1,5-PENTAMETHYLENE DIISOCYANATE | MITSUI CHEMICALS INC (JP) | 2019-10-30 | — | — | EP | disclosed |
| US-10385167-B2 | Process for the synthesis of polyoxazolidinone compounds with high stability | COVESTRO DEUTSCHLAND AG (DE) | 2019-08-20 | — | — | US | disclosed |
| EP-2592069-B1 | METHOD OF PRODUCING TOLUENEDICARBAMATE AND METHOD OF PRODUCING TOLUENEDIISOCYANATE | MITSUI CHEMICALS INC (JP) | 2019-04-24 | — | — | EP | disclosed |
| CN-1126628-A | Simulated moving bed chromatographic separation process | DAICEL CHEM (JP) | 1996-07-17 | — | — | CN | disclosed |
| EP-0606366-A1 | SUBSTITUTED PHENSERINES AND PHENYLCARBAMATES OF (-)-ESEROLINE, (-)-N1-NORESEROLINE, AND (-)-N1-BENZYLNORESEROLINE; AS SPECIFIC INHIBITORS OF ACETYLCHOLINESTERASE | THE GOVERNMENT OF THE UNITED STATES OF AMERICA as represented by THE SECRETARY of the DEPARTMENT OF HEALTH AND HUMAN SERVICES (US) | 1994-07-20 | — | — | EP | disclosed |
| WO-1993006105-A1 | SUBSTITUTED PHENSERINES AND PHENYLCARBAMATES OF (-)-ESEROLINE, (-)-N1-NORESEROLINE, AND (-)-N1-BENZYLNORESEROLINE; AS SPECIFIC INHIBITORS OF ACETYLCHOLINESTERASE | UNITED STATES GOVERNMENT, AS REPRESENTED BY SECRET (US) | 1993-04-01 | — | — | WO | disclosed |
| US-5075208-A | Releasing a photographically useful compound upon reduction | FUJI PHOTO FILM CO., LTD. (JP) | 1991-12-24 | — | — | US | disclosed |
| US-4994363-A | Silver halide light-sensitive material containing a compound releasing a photographically useful group | FUJI PHOTO FILM CO., LTD. (JP) | 1991-02-19 | — | — | US | disclosed |
| US-4840887-A | USEFUL GROUP RELEASED BY CLEAVAGE BETWEEN SULFONYL GROUP AND A NITROGEN, SULFUR OR OXYGEN ATOM; STABILITY | FUJI PHOTO FILM CO., LTD. (JP) | 1989-06-20 | — | — | US | disclosed |
| US-4692550-A | Continuous process for thermal splitting of carbamic acid esters | BAYER AKTIENGESELLSCHAFT (DE) | 1987-09-08 | — | — | US | disclosed |
| US-4497887-A | Thermal development type diazo copying material with hydrophobic resin encapsulated coupler particle | Ricoh Compay, Ltd. (JP) | 1985-02-05 | — | — | US | disclosed |
| US-4226883-A | Carbamate derivatives and method for manufacture thereof | YAMAMOTO IZURU | 1980-10-07 | — | — | US | disclosed |