Predicted protein targets (top 20)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | CA1 | P00915 | 3/20 | 0.43 |
| ▸ | CA2 | P00918 | 3/20 | 0.43 |
| ▸ | CA7 | P43166 | 2/20 | 0.43 |
| ▸ | CA9 | Q16790 | 2/20 | 0.43 |
| ▸ | CA12 | O43570 | 1/20 | 0.43 |
| ▸ | CA4 | P22748 | 1/20 | 0.43 |
| ▸ | CA14 | Q9ULX7 | 1/20 | 0.43 |
| ▸ | POLB | P06746 | 2/20 | 0.37 |
| ▸ | SMN1; SMN2 | Q16637 | 2/20 | 0.37 |
| ▸ | ALDH1A1 | P00352 | 3/20 | 0.36 |
| ▸ | TP53 | P04637 | 1/20 | 0.36 |
| ▸ | TSHR | P16473 | 1/20 | 0.36 |
| ▸ | ADRA2B | P18089 | 1/20 | 0.36 |
| ▸ | PTGS1 | P23219 | 1/20 | 0.36 |
| ▸ | TDP1 | Q9NUW8 | 1/20 | 0.36 |
| ▸ | HTT | P42858 | 2/20 | 0.35 |
| ▸ | L3MBTL1 | Q9Y468 | 2/20 | 0.35 |
| ▸ | MAPK1 | P28482 | 1/20 | 0.35 |
| ▸ | IDO1 | P14902 | 2/20 | 0.35 |
| ▸ | TAAR1 | Q96RJ0 | 1/20 | 0.35 |
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 | |
|---|---|---|---|---|
| SCHEMBL8932160 | 0.88 | CA1 (0.50) | CA1CA2CA7CA9CA12 | |
| SCHEMBL903333 | 0.87 | CA1 (0.44) | CA1CA2CA7CA9CA12 | |
| SCHEMBL1231880 | 0.87 | CA1 (0.44) | CA1CA2CA7CA9CA12 | |
| SCHEMBL30517362 | 0.87 | CA1 (0.44) | CA1CA2CA7CA9CA12 | |
| SCHEMBL29396701 | 0.87 | CA1 (0.44) | CA1CA2CA7CA9CA12 | |
| SCHEMBL25208290 | 0.87 | CA1 (0.44) | CA1CA2CA7CA9CA12 | |
| SCHEMBL30007746 | 0.87 | CA1 (0.44) | CA1CA2CA7CA9CA12 | |
| SCHEMBL10290527 | 0.87 | CA1 (0.44) | CA1CA2CA7CA9CA12 | |
| SCHEMBL31593 | 0.87 | CA1 (0.44) | CA1CA2CA7CA9CA12 | |
| SCHEMBL29367537 | 0.87 | CA1 (0.44) | CA1CA2CA7CA9CA12 |
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 31 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-108003165-A | A kind of synthetic method of 5,11- dihydros -5- Phenylindoles simultaneously [3,2-b] carbazole | 河南省科学院化学研究所有限公司 | 2018-05-08 | — | — | CN | claimed |
| CN-107868089-A | A kind of synthetic method of the Phenylindole of 5,12 dihydro 5 simultaneously [3,2 a] carbazole | 河南省科学院化学研究所有限公司 | 2018-04-03 | — | — | CN | claimed |
| CN-106317111-B | A kind of method of synthesis of chiral 1,2 pairs [(2 methoxyphenyl) phenyl phosphino-] ethane | 河南省科学院化学研究所有限公司 | 2018-01-16 | — | — | CN | claimed |
| CN-105418440-B | A kind of method that the propyl alcohol of 2 amino, 2 methyl 1 is synthesized by isopropylamine | 张家港吉慕特化工科技有限公司 | 2017-08-25 | — | — | CN | claimed |
| CN-106317111-A | Chiral 1,2-bi[(2-methoxy phenyl)phenyl phosphine] ethane synthesis method | 河南省科学院化学研究所有限公司 | 2017-01-11 | — | — | CN | claimed |
| CN-108003165-A | A kind of synthetic method of 5,11- dihydros -5- Phenylindoles simultaneously [3,2-b] carbazole | 河南省科学院化学研究所有限公司 | 2018-05-08 | — | — | CN | disclosed |
| CN-107868089-A | A kind of synthetic method of the Phenylindole of 5,12 dihydro 5 simultaneously [3,2 a] carbazole | 河南省科学院化学研究所有限公司 | 2018-04-03 | — | — | CN | disclosed |
| CN-106317111-B | A kind of method of synthesis of chiral 1,2 pairs [(2 methoxyphenyl) phenyl phosphino-] ethane | 河南省科学院化学研究所有限公司 | 2018-01-16 | — | — | CN | disclosed |
| CN-106317111-B | A kind of method of synthesis of chiral 1,2 pairs [(2 methoxyphenyl) phenyl phosphino-] ethane | 河南省科学院化学研究所有限公司 | 2018-01-16 | — | — | CN | disclosed |
| CN-106317111-B | A kind of method of synthesis of chiral 1,2 pairs [(2 methoxyphenyl) phenyl phosphino-] ethane | 河南省科学院化学研究所有限公司 | 2018-01-16 | — | — | CN | disclosed |
| CN-105418440-B | A kind of method that the propyl alcohol of 2 amino, 2 methyl 1 is synthesized by isopropylamine | 张家港吉慕特化工科技有限公司 | 2017-08-25 | — | — | CN | disclosed |
| CN-107074675-A | Preparation method of chiral 2- [ 1-cyclopropylethyl ] -6-isopropyl-phenol | 四川海思科制药有限公司 | 2017-08-18 | — | — | CN | disclosed |
| CN-102858788-A | Ruthenium complex and method for preparing optically active alcohol compound | TAKASAGO PERFUMERY CO LTD | 2013-01-02 | — | — | CN | disclosed |
| CN-1926083-B | Manufacturing method of optical activity alcohol | KANTO KAGAKU | 2010-12-08 | — | — | CN | disclosed |
| CN-101676294-A | Method for producing ruthenium complex | TAKASAGO PERFUMERY CO LTD | 2010-03-24 | — | — | CN | disclosed |
| CN-101495491-A | Process for producing optically active aminophosphinylbutanoic acid | MEIJI SEIKA KAISHA (JP) | 2009-07-29 | — | — | CN | disclosed |
| CN-1926083-A | Manufacturing method of optical activity alcohol | NAGOYA IND SCIENCE RES INST (JP) | 2007-03-07 | — | — | CN | disclosed |
| CN-1187830-A | Catalyst composition and process for preparation of copolymers of carbon monoxide and olefinically unsaturated compound | SHELL INT RESEARCH (NL) | 1998-07-15 | — | — | CN | disclosed |
| US-5780692-A | CATALYTIC ASYMMETRIC HYDROGENATION OF A BENZOPHENONE; SIMPLIFICATION | TAKASAGO INTERNATIONAL CORPORATION (JP) | 1998-07-14 | — | — | US | disclosed |
| US-5614641-A | USING A PHOSPHINO-CONTAINING RUTHENIUM COMPLEX AS CATALYST | ELF AQUITAINE (FR) | 1997-03-25 | — | — | US | disclosed |