SCHEMBL987275

SCHEMBL987275

COc1ccc(S(C)(=O)=O)cc1C(=O)O

nearest known ligand 0.62

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
LMNA P02545 3/20 0.60
SMN1; SMN2 Q16637 1/20 0.59
MAPK1 P28482 2/20 0.56
APEX1 P27695 1/20 0.56
TSHR P16473 3/20 0.54
ADRA2A P08913 1/20 0.54
CYP2D6 P10635 1/20 0.54
CYP2C9 P11712 1/20 0.54
DRD2 P14416 1/20 0.54
DRD3 P35462 1/20 0.54
HTR2B P41595 1/20 0.54
STAT6 P42226 1/20 0.54
KCNH2 Q12809 1/20 0.54
BLM P54132 1/20 0.53
ALDH1A1 P00352 2/20 0.49
KDM4E B2RXH2 1/20 0.49
HPGD P15428 1/20 0.49
GAA P10253 2/20 0.48
LCK P06239 1/20 0.47
FYN P06241 1/20 0.47

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
SCHEMBL642859 0.86 ALDH1A1 (0.57) LMNASMN1; SMN2MAPK1TSHRADRA2A
SCHEMBL8261355 0.86 SMN1; SMN2 (0.59) LMNASMN1; SMN2MAPK1TSHRADRA2A
SCHEMBL131628 0.85 GAA (0.65) MAPK1APEX1TSHRADRA2ACYP2D6
SCHEMBL31079411 0.85 MAPK1 (0.54) LMNAMAPK1APEX1TSHRALDH1A1
SCHEMBL30219287 0.85 SMN1; SMN2 (0.57) LMNASMN1; SMN2MAPK1TSHRADRA2A
SCHEMBL9598030 0.85 SMN1; SMN2 (0.57) LMNASMN1; SMN2MAPK1TSHRADRA2A
SCHEMBL3220624 0.85 SMN1; SMN2 (0.57) LMNASMN1; SMN2MAPK1TSHRADRA2A
SCHEMBL1364551 0.85 MAPK1 (0.54) LMNAMAPK1APEX1TSHRALDH1A1
SCHEMBL3344597 0.85 SMN1; SMN2 (0.57) LMNASMN1; SMN2MAPK1TSHRADRA2A
Hydrochloric Acid SCHEMBL10988216 0.83 GAA (0.63) MAPK1APEX1TSHRADRA2ACYP2D6

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-3975434-A Processes of producing 2,5-disubstituted benzamides SOCIETE D'ETUDES SCIENTIFIQUES ET INDUSTRIELLES DE L'ILE-DE-FRANCE (FR) 1976-08-17 US claimed
US-20240158372-A1 BISAMIDE SARCOMERE ACTIVATING COMPOUNDS AND USES THEREOF AMGEN INC. 2024-05-16 US disclosed
CN-117126085-A Preparation method of N- [2- (diethylamino) ethyl ] -5- (methylsulfonyl) -2-methoxybenzamide salt 江苏恩华药业股份有限公司 2023-11-28 CN disclosed
US-11780826-B2 Bisamide sarcomere activating compounds and uses thereof AMGEN INC. (US) 2023-10-10 US disclosed
US-20220289685-A1 ANTIMALARIAL HEXAHYDROPYRIMIDINE ANALOGUES UCB BIOPHARMA SRL (SOCIETE A RESPONSABILITE LIMITEE) (BE) 2022-09-15 US disclosed
US-20220281850-A1 BISAMIDE SARCOMERE ACTIVATING COMPOUNDS AND USES THEREOF AMGEN INC. 2022-09-08 US disclosed
EP-4017591-A1 ANTIMALARIAL HEXAHYDROPYRIMIDINE ANALOGUES UCB Biopharma SRL (BE) 2022-06-29 EP disclosed
US-11299479-B1 Bisamide sarcomere activating compounds and uses thereof CYTOKINETICS, INC. (US) 2022-04-12 US disclosed
CN-114206856-A Anti-malarial hexahydropyrimidine analogues UCB生物制药有限责任公司 2022-03-18 CN disclosed
US-11254658-B2 Bisamide sarcomere activating compounds and uses thereof AMGEN INC. (US) 2022-02-22 US disclosed
WO-1997022604-A1 NOVEL SUBSTITUTED 4-(1H-BENZIMIDAZOL-2-YL)[1,4]DIAZEPANES USEFUL FOR THE TREATMENT OF ALLERGIC DISEASES HOECHST MARION ROUSSEL, INC. (US) 1997-06-26 WO disclosed
WO-1997019074-A1 SUBSTITUTED 4-(1H-BENZIMIDAZOL-2-YL-AMINO)PIPERIDINES USEFUL FOR THE TREATMENT OF ALLERGIC DISEASES HOECHST MARION ROUSSEL, INC. (US) 1997-05-29 WO disclosed
US-4935511-A Nervous system, gastrointestinal disorders RORER PHARMACEUTICAL CORPORATION (US) 1990-06-19 US disclosed
US-4673686-A CNS MODIFIERS, ANTI-APOMORPHINE ANTIENETIC ACITIVTY/ SOCIETE D'ETUDES SCIENTIFIQUES ET INDUSTRIELLE DE L'ILE DE FRANCE (FR) 1987-06-16 US disclosed
US-4624961-A LEARNING ENHANCEMENT A. H. ROBINS COMPANY, INCORPORATED (US) 1986-11-25 US disclosed
US-4352802-A DESALINATION OF SEA WATER BEECHAM GROUP LIMITED (GB) 1982-10-05 US disclosed
EP-0041817-A1 Benzamide derivatives, process for their preparation and pharmaceutical compositions containing them BEECHAM GROUP PLC (GB) 1981-12-16 EP disclosed
US-4197243-A ANTIPSYCHOTICS, STRONG CNS DEPRESSANTS YAMANOUCHI PHARMACEUTICAL CO., LTD. (JP) 1980-04-08 US disclosed
US-4097487-A CNS DEPRESSANTS, ANTIPSYCHOTICS YAMANOUCHI PHARMACEUTICAL CO., LTD. (JA) 1978-06-27 US disclosed
US-3975434-A Processes of producing 2,5-disubstituted benzamides SOCIETE D'ETUDES SCIENTIFIQUES ET INDUSTRIELLES DE L'ILE-DE-FRANCE (FR) 1976-08-17 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 (6 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-11254658-B2 Bisamide sarcomere activating compounds and uses thereof TNNI3, TNNT2, TNNC1 LMNA 42/4885SMN1; SMN2 126/4885MAPK1 1704/4885
US-11780826-B2 Bisamide sarcomere activating compounds and uses thereof TNNI3, TNNT2, TNNC1 LMNA 42/4885SMN1; SMN2 126/4885MAPK1 1704/4885
US-20240158372-A1 BISAMIDE SARCOMERE ACTIVATING COMPOUNDS AND USES THEREOF TNNI3, TNNT2, TNNC1 LMNA 42/4885SMN1; SMN2 126/4885MAPK1 1704/4885
US-20220289685-A1 ANTIMALARIAL HEXAHYDROPYRIMIDINE ANALOGUES G6PD, DPYD, DHFR LMNA 3982/4885SMN1; SMN2 3408/4885MAPK1 2090/4885
US-20220281850-A1 BISAMIDE SARCOMERE ACTIVATING COMPOUNDS AND USES THEREOF TNNI3, TNNT2, TNNC1 LMNA 42/4885SMN1; SMN2 126/4885MAPK1 1704/4885
US-11299479-B1 Bisamide sarcomere activating compounds and uses thereof TNNI3, TNNT2, TNNC1 LMNA 42/4885SMN1; SMN2 126/4885MAPK1 1704/4885

“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.