SCHEMBL7051522

SCHEMBL7051522

COc1ccc(C(C)CO)cc1

nearest known ligand 0.70

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ABCB11 O95342 1/20 0.70
ALDH1A1 P00352 2/20 0.51
GAA P10253 1/20 0.51
MAPT P10636 1/20 0.51
TSHR P16473 2/20 0.48
CYP2C9 P11712 1/20 0.48
CA1 P00915 2/20 0.48
CA2 P00918 2/20 0.48
CA12 O43570 1/20 0.48
CA7 P43166 1/20 0.48
CA9 Q16790 1/20 0.48
CA14 Q9ULX7 1/20 0.48
AOC3 Q16853 2/20 0.47
GPR88 Q9GZN0 1/20 0.46
L3MBTL1 Q9Y468 2/20 0.46
ACHE P22303 1/20 0.46
CYP1A2 P05177 1/20 0.46
CYP2D6 P10635 1/20 0.46
CYP2C19 P33261 1/20 0.46
MAPK1 P28482 1/20 0.45

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.

Compoundsimilaritytop predictedshared targets
SCHEMBL7419755 1.00 ABCB11 (0.70) ABCB11ALDH1A1GAAMAPTTSHR
SCHEMBL6680649 0.84 ABCB11 (0.56) ABCB11ALDH1A1GAAMAPTTSHR
SCHEMBL11705595 0.83 ABCB11 (0.51) ABCB11ALDH1A1GAAMAPTTSHR
SCHEMBL2641075 0.83 ABCB11 (0.52) ABCB11TSHRCYP2C9ACHETDP1
Naproxol SCHEMBL29979997 0.83 ABCB11 (1.00) ABCB11MAPTTSHRCYP2C9L3MBTL1
Naproxol SCHEMBL30599771 0.83 ABCB11 (1.00) ABCB11MAPTTSHRCYP2C9L3MBTL1
Naproxol SCHEMBL43203 0.83 ABCB11 (1.00) ABCB11MAPTTSHRCYP2C9L3MBTL1
Naproxol SCHEMBL10395753 0.83 ABCB11 (1.00) ABCB11MAPTTSHRCYP2C9L3MBTL1
Naproxol SCHEMBL8471214 0.83 ABCB11 (1.00) ABCB11MAPTTSHRCYP2C9L3MBTL1
SCHEMBL4454111 0.82 CA1 (0.52) ABCB11ALDH1A1GAAMAPTTSHR

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 21 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-118955244-A Method for preparing primary alcohol by homogeneously catalyzing and reducing carboxylic acid derivative by using N-heterocyclic carbene copper complex 延安大学 2024-11-15 CN disclosed
EP-3365334-B1 BENZOLACTAM COMPOUNDS AS PROTEIN KINASE INHIBITORS OTSUKA PHARMA CO LTD (JP) 2024-07-17 EP disclosed
CN-117751155-A Copolymerization of aldehydes and vinyl ethers 巴斯夫欧洲公司 2024-03-22 CN disclosed
CN-117440986-A Polyisobutene having a high content of specific double bond isomers 巴斯夫欧洲公司 2024-01-23 CN disclosed
CN-113698514-B Process for preparing highly reactive isobutylene homo-or copolymers 巴斯夫欧洲公司 2023-11-10 CN disclosed
CN-116075531-A Process for preparing highly reactive isobutylene homo-or copolymers 巴斯夫欧洲公司 2023-05-05 CN disclosed
US-20230019032-A1 BENZOLACTAM COMPOUNDS AS PROTEIN KINASE INHIBITORS OTSUKA PHARMACEUTICAL CO., LTD. (JP) 2023-01-19 US disclosed
CN-108602913-B Method for producing highly reactive isobutene homo-or copolymers 巴斯夫欧洲公司 2022-07-08 CN disclosed
CN-113698514-A Method for producing highly reactive isobutene homo-or copolymers 巴斯夫欧洲公司 2021-11-26 CN disclosed
CN-109415452-B Method for producing highly reactive isobutene homo-or copolymers 巴斯夫欧洲公司 2021-10-26 CN disclosed
CN-110997737-A Method for producing highly reactive isobutene homo-or copolymers 巴斯夫欧洲公司 2020-04-10 CN disclosed
US-10457669-B2 Benzolactam compounds as protein kinase inhibitors OTSUKA PHARMACEUTICAL CO., LTD. (JP) 2019-10-29 US disclosed
CN-109415452-A The method for preparing highly reactive isobutylene homo or copolymer 巴斯夫欧洲公司 2019-03-01 CN disclosed
US-20190047990-A1 BENZOLACTAM COMPOUNDS AS PROTEIN KINASE INHIBITORS OTSUKA PHARMACEUTICAL CO., LTD. (JP) 2019-02-14 US disclosed
CN-108602913-A The method for preparing highly reactive isobutylene homo or copolymer 巴斯夫欧洲公司 2018-09-28 CN disclosed
CN-108602914-A Method for producing highly reactive isobutene homo-or copolymers 巴斯夫欧洲公司 2018-09-28 CN disclosed
EP-0882715-B1 NOVEL N-(UNSUBSTITUTED OR SUBSTITUTED)-4-SUBSTITUTED-6-(UNSUBSTITUTED OR SUBSTITUTED)PHENOXY-2-PYRIDINECARBOXAMIDES OR THIOCARBOXAMIDES, PROCESSES FOR PRODUCING THE SAME, AND HERBICIDES KUREHA CHEMICAL IND CO LTD (JP) 2003-04-23 EP disclosed
US-6339045-B1 CAN BE USED IN A SMALL AMOUNT, SHOWING A GOOD SELECTIVITY BETWEEN CROP AND WEED, AND CAUSING NO PHYTOTOXICITY KUREHA KAGAKU KOGYO KABUSHIKI KAISHA (JP) 2002-01-15 US disclosed
EP-0882715-A1 NOVEL N-(UNSUBSTITUTED OR SUBSTITUTED)-4-SUBSTITUTED-6-(UNSUBSTITUTED OR SUBSTITUTED)PHENOXY-2-PYRIDINECARBOXAMIDES OR THIOCARBOXAMIDES, PROCESSES FOR PRODUCING THE SAME, AND HERBICIDES KUREHA KAGAKU KOGYO KABUSHIKI KAISHA (JP) 1998-12-09 EP disclosed
US-4151179-A ANTIINFLAMMATORY AGENTS FISONS LIMITED (GB) 1979-04-24 US 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 (3 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.

PatentTitleText reads most aboutPredicted target · text-rank
US-20230019032-A1 BENZOLACTAM COMPOUNDS AS PROTEIN KINASE INHIBITORS MAPK1, ALK, MAP3K1 ABCB11 2337/4885ALDH1A1 1598/4885GAA 4612/4885
US-20190047990-A1 BENZOLACTAM COMPOUNDS AS PROTEIN KINASE INHIBITORS MAPK1, ALK, MAP3K1 ABCB11 2337/4885ALDH1A1 1598/4885GAA 4612/4885
US-10457669-B2 Benzolactam compounds as protein kinase inhibitors MAPK1, ALK, MAP3K1 ABCB11 2337/4885ALDH1A1 1598/4885GAA 4612/4885

“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.