SCHEMBL309673

SCHEMBL309673

COc1cccc(NS(C)(=O)=O)c1

nearest known ligand 0.60

Predicted protein targets (top 19)

geneUniProtsupporting neighboursconfidence
LMNA P02545 6/20 0.60
SMN1; SMN2 Q16637 4/20 0.60
MEN1 O00255 3/20 0.60
KMT2A Q03164 3/20 0.60
TSHR P16473 1/20 0.60
HTT P42858 1/20 0.60
PTGS1 P23219 1/20 0.59
ALDH1A1 P00352 4/20 0.59
POLB P06746 2/20 0.58
PKM P14618 2/20 0.56
HPGD P15428 2/20 0.56
CYP19A1 P11511 1/20 0.56
KEAP1 Q14145 1/20 0.53
DRD2 P14416 1/20 0.52
DRD4 P21917 1/20 0.52
DRD3 P35462 1/20 0.52
PGR P06401 1/20 0.51
GAA P10253 1/20 0.51
MAPK1 P28482 1/20 0.51

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
Hydrochloric Acid SCHEMBL20502482 0.98 LMNA (0.59) LMNASMN1; SMN2MEN1KMT2ATSHR
SCHEMBL10416921 0.89 PGR (0.61) LMNASMN1; SMN2MEN1KMT2ATSHR
SCHEMBL4204011 0.87 PGR (0.62) LMNASMN1; SMN2MEN1KMT2ATSHR
SCHEMBL27363449 0.84 POLB (0.53) LMNASMN1; SMN2MEN1KMT2ATSHR
SCHEMBL21033859 0.84 LMNA (0.59) LMNASMN1; SMN2MEN1KMT2ATSHR
SCHEMBL11785316 0.84 LMNA (0.59) LMNASMN1; SMN2MEN1KMT2ATSHR
SCHEMBL5763668 0.84 LMNA (0.59) LMNASMN1; SMN2MEN1KMT2ATSHR
SCHEMBL1645211 0.84 CA1 (0.62) LMNASMN1; SMN2MEN1KMT2ATSHR
SCHEMBL28082173 0.83 TSHR (0.74) LMNASMN1; SMN2MEN1KMT2ATSHR
SCHEMBL17227610 0.82 LMNA (0.61) LMNASMN1; SMN2MEN1KMT2ATSHR

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-4258191-A STARTING WITH 4-BUTYRYLAMINO-3-METHOXY-NITROBENZENE THE UNITED STATES OF AMERICA AS REPRESENTED BY THE SECRETARY OF HEALTH, EDUCATION AND WELFARE (US) 1981-03-24 US claimed
US-20230348441-A1 BICYCLIC COMPOUND THAT ACTS AS CRBN PROTEIN REGULATOR MEDSHINE DISCOVERY INC. (CN) 2023-11-02 US disclosed
US-11744832-B2 Heteroaryl substituted pyrrolo[2,3-b]pyridines and pyrrolo[2,3-b]pyrimidines as Janus kinase inhibitors INCYTE CORPORATION (US) 2023-09-05 US disclosed
US-20220395506-A1 HETEROARYL SUBSTITUTED PYRROLO[2,3-b]PYRIDINES AND PYRROLO[2,3-b]PYRIMIDINES AS JANUS KINASE INHIBITORS INCYTE CORPORATION 2022-12-15 US disclosed
EP-3328843-B1 1,3,4-OXADIAZOLE SULFONAMIDE DERIVATIVE COMPOUNDS AS HISTONE DEACETYLASE 6 INHIBITOR, AND THE PHARMACEUTICAL COMPOSITION COMPRISING THE SAME CHONG KUN DANG PHARMACEUTICAL CORP (KR) 2022-10-26 EP disclosed
US-11331320-B2 Heteroaryl substituted pyrrolo[2,3-b]pyridines and pyrrolo[2,3-b]pyrimidines as Janus kinase inhibitors INCYTE HOLDINGS CORPORATION (US) 2022-05-17 US disclosed
CN-107922362-B 1,3, 4-oxadiazole sulfonamide derivative compounds as histone deacetylase 6 inhibitors and pharmaceutical compositions containing the same 株式会社钟根堂 2021-06-15 CN disclosed
WO-2021047674-A1 BICYCLIC COMPOUND THAT ACTS AS CRBN PROTEIN REGULATOR 南京明德新药研发有限公司 2021-03-18 WO disclosed
US-20200338077-A1 HETEROARYL SUBSTITUTED PYRROLO[2,3-b]PYRIDINES AND PYRROLO[2,3-b]PYRIMIDINES AS JANUS KINASE INHIBITORS INCYTE CORPORATION 2020-10-29 US disclosed
US-20180251437-A1 1,3,4-OXADIAZOLE SULFONAMIDE DERIVATIVE COMPOUNDS AS HISTONE DEACETYLASE 6 INHIBITOR, AND THE PHARMACEUTICAL COMPOSITION COMPRISING THE SAME CHONG KUN DANG PHARMACEUTICAL CORP. (KR) 2018-09-06 US disclosed
WO-2001064634-A1 PHARMACEUTICAL COMPOSITIONS CONTAINING AZETIDINE DERIVATIVES, NOVEL AZETIDINE DERIVATIVES AND PREPARATION THEREOF AVENTIS PHARMA S.A. (FR) 2001-09-07 WO disclosed
EP-0142085-B1 METHOD OF PREPARING MICROSPHERES FOR INTRAVASCULAR DELIVERY Mosier, Benjamin (US) 1988-08-24 EP disclosed
US-4704397-A ANTITUMOR AGENTS WARNER-LAMBERT COMPANY (US) 1987-11-03 US disclosed
EP-0142085-A2 Method of preparing microspheres for intravascular delivery Mosier, Benjamin (US) 1985-05-22 EP disclosed
US-4492720-A DISSOLVING, DISPERSION IN MATRIX, EVAPORATION OF SOLVENT MOSIER BENJAMIN 1985-01-08 US disclosed
EP-0035862-B1 PHARMACEUTICALLY ACCEPTABLE SALTS OF 4'-(9-ACRIDINYLAMINO) METHANESULFON-M-ANISIDIDE, THEIR PRODUCTION, AND PHARMACEUTICAL COMPOSITIONS CONTAINING SUCH SALTS WARNER-LAMBERT COMPANY (US) 1984-06-13 EP disclosed
US-4399283-A ANTITIMOR AGENTS WARNER LAMBERT COMPANY (US) 1983-08-16 US disclosed
US-4258191-A STARTING WITH 4-BUTYRYLAMINO-3-METHOXY-NITROBENZENE THE UNITED STATES OF AMERICA AS REPRESENTED BY THE SECRETARY OF HEALTH, EDUCATION AND WELFARE (US) 1981-03-24 US disclosed
US-4258191-A STARTING WITH 4-BUTYRYLAMINO-3-METHOXY-NITROBENZENE THE UNITED STATES OF AMERICA AS REPRESENTED BY THE SECRETARY OF HEALTH, EDUCATION AND WELFARE (US) 1981-03-24 US disclosed
US-4258191-A STARTING WITH 4-BUTYRYLAMINO-3-METHOXY-NITROBENZENE THE UNITED STATES OF AMERICA AS REPRESENTED BY THE SECRETARY OF HEALTH, EDUCATION AND WELFARE (US) 1981-03-24 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 (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-20200338077-A1 HETEROARYL SUBSTITUTED PYRROLO[2,3-b]PYRIDINES AND PYRROLO[2,3-b]PYRIMIDINES AS JANUS KINASE INHIBITORS JAK3, JAK1, JAK2 LMNA 4785/4885SMN1; SMN2 3741/4885MEN1 3406/4885
US-20180251437-A1 1,3,4-OXADIAZOLE SULFONAMIDE DERIVATIVE COMPOUNDS AS HISTONE DEACETYLASE 6 INHIBITOR, AND THE PHARMACEUTICAL COMPOSITION COMPRISING THE SAME HDAC1, HDAC6, HDAC2 LMNA 3360/4885SMN1; SMN2 1602/4885MEN1 4654/4885
US-20230348441-A1 BICYCLIC COMPOUND THAT ACTS AS CRBN PROTEIN REGULATOR CRBN, CRKL, NCOR1 LMNA 3513/4885SMN1; SMN2 2827/4885MEN1 3717/4885
US-20220395506-A1 HETEROARYL SUBSTITUTED PYRROLO[2,3-b]PYRIDINES AND PYRROLO[2,3-b]PYRIMIDINES AS JANUS KINASE INHIBITORS JAK3, JAK1, JAK2 LMNA 4785/4885SMN1; SMN2 3741/4885MEN1 3406/4885
US-11744832-B2 Heteroaryl substituted pyrrolo[2,3-b]pyridines and pyrrolo[2,3-b]pyrimidines as Janus kinase inhibitors JAK3, JAK1, JAK2 LMNA 4785/4885SMN1; SMN2 3741/4885MEN1 3406/4885
US-11331320-B2 Heteroaryl substituted pyrrolo[2,3-b]pyridines and pyrrolo[2,3-b]pyrimidines as Janus kinase inhibitors JAK3, JAK1, JAK2 LMNA 4785/4885SMN1; SMN2 3741/4885MEN1 3406/4885

“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.