SCHEMBL85199

SCHEMBL85199

CC(C)C(=O)NS(=O)(=O)c1ccccc1

nearest known ligand 0.69

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 3/20 0.69
LARS1 Q9P2J5 2/20 0.64
NPSR1 Q6W5P4 1/20 0.63
TARS1 P26639 1/20 0.52
CA2 P00918 2/20 0.51
HPGD P15428 2/20 0.51
LMNA P02545 2/20 0.51
SMN1; SMN2 Q16637 2/20 0.51
MITF O75030 2/20 0.51
KMT2A Q03164 1/20 0.51
KDM4E B2RXH2 2/20 0.50
MMP2 P08253 2/20 0.50
PTGS1 P23219 2/20 0.50
PTGS2 P35354 2/20 0.50
BCAT1 P54687 1/20 0.50
CA1 P00915 1/20 0.50
MMP1 P03956 1/20 0.50
MMP9 P14780 1/20 0.50
MMP8 P22894 1/20 0.50
MMP13 P45452 1/20 0.50

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
SCHEMBL17123491 0.90 ALDH1A1 (0.66) ALDH1A1LARS1NPSR1TARS1CA2
SCHEMBL9885774 0.87 LARS1 (0.69) ALDH1A1LARS1NPSR1TARS1LMNA
SCHEMBL17286576 0.85 TARS1 (0.73) ALDH1A1LARS1NPSR1TARS1LMNA
SCHEMBL19627411 0.84 ALDH1A1 (0.68) ALDH1A1LARS1NPSR1TARS1CA2
SCHEMBL8277097 0.83 ALDH1A1 (0.72) ALDH1A1NPSR1CA2LMNASMN1; SMN2
SCHEMBL8284971 0.82 LARS1 (0.66) ALDH1A1LARS1NPSR1TARS1CA2
SCHEMBL29950584 0.82 ALDH1A1 (0.66) ALDH1A1LARS1NPSR1TARS1CA2
SCHEMBL5663334 0.82 LARS1 (0.57) ALDH1A1LARS1NPSR1TARS1CA2
SCHEMBL13768086 0.82 LARS1 (0.61) ALDH1A1LARS1NPSR1TARS1CA2
SCHEMBL17286571 0.82 CA1 (0.57) ALDH1A1LARS1CA2KMT2AKDM4E

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-116444420-A Small molecule inhibitor of beta-catenin/BCL 9 protein interaction and application thereof 上海医药工业研究院有限公司 2023-07-18 CN claimed
CN-116162056-A Small molecule inhibitor of beta-catenin/BCL 9 protein-protein interaction and application thereof 上海医药工业研究院 2023-05-26 CN claimed
WO-2024217513-A1 β-CATENIN/BCL9 PROTEIN-PROTEIN INTERACTION INHIBITOR, PREPARATION METHOD THEREFOR AND USE THEREOF 复旦大学 2024-10-24 WO disclosed
US-20240287029-A1 SULFONAMIDES, METHOD FOR PREPARATION THEREOF, AND USE THEREOF CHENGDU SHIBEIKANG BIOMEDICAL TECHNOLOGY CO., LTD. (CN) 2024-08-29 US disclosed
EP-4410786-A1 SULFONAMIDE COMPOUND, PREPARATION METHOD THEREFOR AND USE THEREOF Chengdu Shibeikang Biomedical Technology Co., Ltd. (CN) 2024-08-07 EP disclosed
CN-116444420-A Small molecule inhibitor of beta-catenin/BCL 9 protein interaction and application thereof 上海医药工业研究院有限公司 2023-07-18 CN disclosed
CN-116162056-A Small molecule inhibitor of beta-catenin/BCL 9 protein-protein interaction and application thereof 上海医药工业研究院 2023-05-26 CN disclosed
WO-2023046150-A1 SULFONAMIDE COMPOUND, PREPARATION METHOD THEREFOR AND USE THEREOF 成都施贝康生物医药科技有限公司 2023-03-30 WO disclosed
US-20230039309-A1 SUBSTITUTED INDOLE MCL-1 INHIBITORS VANDERBILT UNIVERSITY 2023-02-09 US disclosed
CN-113773300-B Sulfonamide compound, preparation method and application thereof 成都施贝康生物医药科技有限公司 2022-10-11 CN disclosed
US-20210363155-A1 4-PHENYLPIPERIDINES, THEIR PREPARATION AND USE THE TRUSTEES OF COLUMBIA UNIVERSITY IN THE CITY OF NEW YORK (US) 2021-11-25 US disclosed
US-20070259929-A1 Therapeutic Compounds ALLERGAN, INC. 2007-11-08 US disclosed
US-20070259929-A1 Therapeutic Compounds ALLERGAN, INC. 2007-11-08 US disclosed
US-20070259947-A1 THERAPEUTIC COMPOUNDS ALLERGAN, INC. 2007-11-08 US disclosed
US-20070043021-A1 derivatives of 2-methyl-4-(4-methyl-1-piperazinyl)-10H-thieno[2,3-b][1,5]benzodiazepine for modulating sleep disorder; side effect reduction HYPNION, INC. 2007-02-22 US disclosed
US-20070004752-A1 Benzisoxazole piperazine compounds and methods of use thereof HYPNION, INC. 2007-01-04 US disclosed
US-20070004752-A1 Benzisoxazole piperazine compounds and methods of use thereof HYPNION, INC. 2007-01-04 US disclosed
US-4495365-A N-Acylsulfonamide herbicidal antidotes STAUFFER CHEMICAL CO. (US) 1985-01-22 US disclosed
US-4347380-A N-Acylsulfonamide herbicidal antidotes STAUFFER CHEMICAL COMPANY (US) 1982-08-31 US disclosed
US-4266078-A N-Acylsulfonamide herbicidal antidotes STAUFFER CHEMICAL COMPANY (US) 1981-05-05 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 (7 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-20070043021-A1 derivatives of 2-methyl-4-(4-methyl-1-piperazinyl)-10H-thieno[2,3-b][1,5]benzodiazepine for modulating sleep disorder; side effect reduction GABRB3, GRIN2C, GABRB2 ALDH1A1 1166/4885LARS1 4854/4885NPSR1 86/4885
US-20070004752-A1 Benzisoxazole piperazine compounds and methods of use thereof GABRA5, HCRTR2, HCRTR1 ALDH1A1 1540/4885LARS1 4865/4885NPSR1 205/4885
US-20240287029-A1 SULFONAMIDES, METHOD FOR PREPARATION THEREOF, AND USE THEREOF P2RX3, P2RX5, P2RX2 ALDH1A1 2252/4885LARS1 3215/4885NPSR1 89/4885
US-20070259929-A1 Therapeutic Compounds PIGO, CYC1, COXFA4L2 ALDH1A1 747/4885LARS1 2365/4885NPSR1 2050/4885
US-20210363155-A1 4-PHENYLPIPERIDINES, THEIR PREPARATION AND USE HTR3C, HRH4, CYP4F3 ALDH1A1 2713/4885LARS1 3929/4885NPSR1 235/4885
US-20230039309-A1 SUBSTITUTED INDOLE MCL-1 INHIBITORS MCL1, BCL2L1, BCL3 ALDH1A1 1900/4885LARS1 2925/4885NPSR1 4187/4885
US-20070259947-A1 THERAPEUTIC COMPOUNDS GOT2, ANXA5, MMP8 ALDH1A1 840/4885LARS1 2847/4885NPSR1 2506/4885

“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.