SCHEMBL88860

SCHEMBL88860

[O-][S+]1CCNc2ccccc21

nearest known ligand 0.35

Predicted protein targets (top 9)

geneUniProtsupporting neighboursconfidence
MEN1 O00255 2/20 0.34
GAA P10253 2/20 0.34
KMT2A Q03164 2/20 0.34
ALDH1A1 P00352 1/20 0.34
KDM4E B2RXH2 1/20 0.31
NPC1 O15118 1/20 0.31
MAPT P10636 1/20 0.31
RXFP1 Q9HBX9 1/20 0.31
KDM1A O60341 1/20 0.30

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
SCHEMBL7347184 0.88 MEN1 (0.32) MEN1GAAKMT2AALDH1A1
SCHEMBL13477741 0.88 MEN1 (0.32) MEN1GAAKMT2AALDH1A1
SCHEMBL9630852 0.86 MEN1 (0.32) MEN1GAAKMT2AALDH1A1
SCHEMBL83412 0.78 ALOX15 (0.30)
Hydrochloric Acid SCHEMBL9449441 0.77 MEN1 (0.31) MEN1GAAKMT2AALDH1A1
Hydrochloric Acid SCHEMBL27353718 0.77 MEN1 (0.31) MEN1GAAKMT2AALDH1A1
SCHEMBL4622490 0.77
SCHEMBL20100281 0.75 CHRNB2 (0.32)
SCHEMBL9879110 0.73 PARP1 (0.46)
SCHEMBL7347191 0.71 MEN1 (0.32) MEN1GAAKMT2AALDH1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-119285574-A Method for preparing 3, 4-dihydro-2H-benzo [ b ] [1,4] thiazine-1-oxide by cooperation of monopersulfate 绍兴文理学院 2025-01-10 CN claimed
CN-119285574-A Method for preparing 3, 4-dihydro-2H-benzo [ b ] [1,4] thiazine-1-oxide by cooperation of monopersulfate 绍兴文理学院 2025-01-10 CN disclosed
CN-119285574-A Method for preparing 3, 4-dihydro-2H-benzo [ b ] [1,4] thiazine-1-oxide by cooperation of monopersulfate 绍兴文理学院 2025-01-10 CN disclosed
CN-119285574-A Method for preparing 3, 4-dihydro-2H-benzo [ b ] [1,4] thiazine-1-oxide by cooperation of monopersulfate 绍兴文理学院 2025-01-10 CN disclosed
WO-2024126453-A1 NEW SUBSTITUTED INDOLE-2-CARBOXAMIDES AS PHGDH INHIBITORS BOEHRINGER INGELHEIM INTERNATIONAL GMBH (DE) 2024-06-20 WO disclosed
WO-2024089006-A1 HETEROCYCLIC COMPOUNDS CAPABLE OF ACTIVATING STING BOEHRINGER INGELHEIM INTERNATIONAL GMBH (DE) 2024-05-02 WO disclosed
WO-2024089008-A1 HETEROCYCLIC COMPOUNDS CAPABLE OF ACTIVATING STING BOEHRINGER INGELHEIM INTERNATIONAL GMBH (DE) 2024-05-02 WO disclosed
WO-2024088991-A1 HETEROCYCLIC COMPOUNDS CAPABLE OF ACTIVATING STING BOEHRINGER INGELHEIM INTERNATIONAL GMBH (DE) 2024-05-02 WO disclosed
WO-2024089155-A1 HETEROCYCLIC COMPOUNDS AS STING ANTAGONISTS BOEHRINGER INGELHEIM INTERNATIONAL GMBH (DE) 2024-05-02 WO disclosed
US-11814380-B2 Benzylamino substituted pyridopyrimidinones and derivatives as SOS1 inhibitors BOEHRINGER INGELHEIM INTERNATIONAL GMBH (DE) 2023-11-14 US disclosed
US-20090312304-A1 ORGANIC COMPOUNDS NOVARTIS AG (CH) 2009-12-17 US disclosed
US-20090281161-A1 Organic Compounds MAIBAUM JUERGEN KLAUS 2009-11-12 US disclosed
US-20090270417-A1 Organic Compounds NOVARTIS AG (CH) 2009-10-29 US disclosed
US-20090247577-A1 PYRROLIDINE DERIVATIVES USEFUL AS BACE INHIBITORS ROGEL OLIVIER 2009-10-01 US disclosed
US-20090233920-A1 ORGANIC COMPOUNDS NOVARTIS AG (CH) 2009-09-17 US disclosed
US-7576099-B2 Amide derivatives as ion-channel ligands and pharmaceutical compositions and methods of using the same RENOVIS, INC. (US) 2009-08-18 US disclosed
US-7576099-B2 Amide derivatives as ion-channel ligands and pharmaceutical compositions and methods of using the same RENOVIS, INC. (US) 2009-08-18 US disclosed
US-20090192148-A1 Organic Compounds NOVARTIS AG (CH) 2009-07-30 US disclosed
EP-1027347-A2 3-AMINOALKYLAMINO-2H-1,4-BENZOXA(THIA-)ZINES AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM NEUROGEN CORPORATION (US) 2000-08-16 EP disclosed
WO-1999023092-A2 3-AMINOALKYLAMINO-2H-1,4-BENZOXA(THIA-)ZINES AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM NEUROGEN CORPORATION (US) 1999-05-14 WO 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-20090247577-A1 PYRROLIDINE DERIVATIVES USEFUL AS BACE INHIBITORS BACE1, BACE2, APP MEN1 2753/4885GAA 47/4885KMT2A 3683/4885
US-20090233920-A1 ORGANIC COMPOUNDS REN, ACE, AGTR1 MEN1 2386/4885GAA 353/4885KMT2A 3192/4885
US-20090192148-A1 Organic Compounds REN, ACE, AGTR1 MEN1 2336/4885GAA 309/4885KMT2A 3129/4885
US-20090281161-A1 Organic Compounds REN, ACE, OTC MEN1 2965/4885GAA 147/4885KMT2A 3953/4885
US-20090270417-A1 Organic Compounds REN, ACE, OTC MEN1 2965/4885GAA 147/4885KMT2A 3953/4885
US-11814380-B2 Benzylamino substituted pyridopyrimidinones and derivatives as SOS1 inhibitors SOS1, SOST, BMP1 MEN1 112/4885GAA 3390/4885KMT2A 2989/4885
US-20090312304-A1 ORGANIC COMPOUNDS REN, ACE, PIGO MEN1 2792/4885GAA 78/4885KMT2A 3979/4885

“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.