SCHEMBL5599840

SCHEMBL5599840

COC(CNS(=O)(=O)c1ccc(C)cc1)OC

nearest known ligand 0.66

Predicted protein targets (top 17)

geneUniProtsupporting neighboursconfidence
▸ MEN1 O00255 2/20 0.66
▸ KMT2A Q03164 2/20 0.66
▸ GBA1 P04062 1/20 0.63
▸ ALDH1A1 P00352 10/20 0.62
▸ TSHR P16473 1/20 0.61
▸ LMNA P02545 1/20 0.54
▸ HPGD P15428 1/20 0.54
▸ HTT P42858 1/20 0.54
▸ CA12 O43570 2/20 0.51
▸ CA9 Q16790 2/20 0.51
▸ CA2 P00918 1/20 0.51
▸ ALOX15 P16050 1/20 0.50
▸ CYP1A2 P05177 1/20 0.50
▸ CYP3A4 P08684 1/20 0.50
▸ ATM Q13315 1/20 0.50
▸ L3MBTL1 Q9Y468 1/20 0.50
▸ CYP19A1 P11511 1/20 0.49

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
SCHEMBL6595288 0.85 MEN1 (0.64) MEN1KMT2AGBA1ALDH1A1TSHR
SCHEMBL17255140 0.84 KMT2A (0.63) MEN1KMT2AGBA1ALDH1A1TSHR
SCHEMBL30569570 0.83 GBA1 (0.59) MEN1KMT2AGBA1ALDH1A1TSHR
SCHEMBL19392455 0.82 MEN1 (0.61) MEN1KMT2AALDH1A1LMNAHPGD
SCHEMBL29960153 0.81 MEN1 (0.59) MEN1KMT2AALDH1A1LMNACA12
SCHEMBL21132292 0.81 GBA1 (0.56) MEN1KMT2AGBA1ALDH1A1TSHR
SCHEMBL7862567 0.80 GBA1 (0.74) MEN1KMT2AGBA1ALDH1A1TSHR
SCHEMBL29543465 0.79 GBA1 (0.72) MEN1KMT2AGBA1ALDH1A1TSHR
SCHEMBL28686588 0.79 GBA1 (0.67) MEN1KMT2AGBA1ALDH1A1TSHR
SCHEMBL17206014 0.79 GBA1 (0.67) MEN1KMT2AGBA1ALDH1A1TSHR

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 20 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-119954810-A Regulator of fused ring derivative, preparation method and application thereof 上海翰森生物医药科技有限公司 2025-05-09 — — CN disclosed
CN-112771025-B Deuterated compounds as ROCK inhibitors 重庆复创医药研究有限公司 2024-02-27 — — CN disclosed
WO-2023217230-A1 KINESIN KIF18A INHIBITOR AND USE THEREOF 上海湃隆生物科技有限公司 2023-11-16 — — WO disclosed
US-20230250080-A1 ENZYME INHIBITORS KALVISTA PHARMACEUTICALS LTD (GB) 2023-08-10 — — US disclosed
US-11613527-B2 Enzyme inhibitors KALVISTA PHARMACEUTICALS LIMITED (GB) 2023-03-28 — — US disclosed
EP-4010333-A1 PLASMA KALLIKREIN INHIBITORS Kalvista Pharmaceuticals Limited (GB) 2022-06-15 — — EP disclosed
CN-114206852-A Plasma kallikrein inhibitors 卡尔维斯塔制药有限公司 2022-03-18 — — CN disclosed
US-20220048894-A1 ENZYME INHIBITORS KALVISTA PHARMACEUTICALS LIMITED (GB) 2022-02-17 — — US disclosed
US-20070032537-A1 5-Substituted 2h-pyrazole-3-carboxylic acid derivatives as agonists for the acid receptor rup25 for the treatment of dyslipidemia and related diseases ARENA PHARMACEUTICALS, INC. (US) 2007-02-08 — — US disclosed
US-20070032537-A1 5-Substituted 2h-pyrazole-3-carboxylic acid derivatives as agonists for the acid receptor rup25 for the treatment of dyslipidemia and related diseases ARENA PHARMACEUTICALS, INC. (US) 2007-02-08 — — US disclosed
US-20070032537-A1 5-Substituted 2h-pyrazole-3-carboxylic acid derivatives as agonists for the acid receptor rup25 for the treatment of dyslipidemia and related diseases ARENA PHARMACEUTICALS, INC. (US) 2007-02-08 — — US disclosed
EP-1633351-A1 5-SUBSTITUTED 2H-PYRAZOLE-3-CARBOXYLIC ACID DERIVATIVES AS AGONISTS FOR THE NICOTINIC ACID RECEPTOR RUP25 FOR THE TREATMENT OF DYSLIPIDEMIA AND RELATED DISEASES Arena Pharmaceuticals, Inc. (US) 2006-03-15 — — EP disclosed
WO-2005011677-A1 5-SUBSTITUTED 2H-PYRAZOLE-3-CARBOXYLIC ACID DERIVATIVES AS AGONISTS FOR THE NICOTINIC ACID RECEPTOR RUP25 FOR THE TREATMENT OF DYSLIPIDEMIA AND RELATED DISEASES ARENA PHARMACEUTICALS, INC. (US) 2005-02-10 — — WO disclosed
US-6825181-B1 ORALLY ADMINISTRATED TO EXHIBIT A STRONG ANTICOAGULANT EFFECT BY INHIBITING ACTIVATED BLOOD- COAGULATION FACTOR X AJINOMOTO CO., INC. (JP) 2004-11-30 — — US disclosed
EP-1065200-A1 AMINOISOQUINOLINE DERIVATIVES Ajinomoto Co., Inc. (JP) 2001-01-03 — — EP disclosed
EP-0757061-B1 Sulfonamido substituted acetal polymers and use thereof in photosensitive compositions and lithographic printing plates KODAK POLYCHROME GRAPHICS LLC (US) 2000-09-13 — — EP disclosed
US-5849842-A Sulfonamido substituted acetal polymers KODAK POLYCHROME GRAPHICS, LLC (US) 1998-12-15 — — US disclosed
US-5698360-A Sulfonamido substituted acetal polymers and use thereof in photo-sensitive compositions and lithographic printing plates SUN CHEMICAL CORPORATION (US) 1997-12-16 — — US disclosed
EP-0757061-A2 Sulfonamido substituted acetal polymers and use thereof in photosensitive compositions and lithographic printing plates SUN CHEMICAL CORPORATION (US) 1997-02-05 — — EP disclosed
US-3969358-A Process for the preparation of thieno [3,2-c] pyridine and thieno [2,3-c] py PARCOR (FR) 1976-07-13 — — 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 (4 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-20230250080-A1 ENZYME INHIBITORS SERPINB1, KLKB1, SERPINE1 MEN1 602/4885KMT2A 1556/4885GBA1 237/4885
US-11613527-B2 Enzyme inhibitors SERPINB1, KLKB1, SERPINE1 MEN1 602/4885KMT2A 1556/4885GBA1 237/4885
US-20070032537-A1 5-Substituted 2h-pyrazole-3-carboxylic acid derivatives as agonists for the acid receptor rup25 for the treatment of dyslipidemia and related diseases ACE, AGTR2, ACE2 MEN1 4781/4885KMT2A 3934/4885GBA1 537/4885
US-20220048894-A1 ENZYME INHIBITORS SERPINB1, KLKB1, SERPINE1 MEN1 602/4885KMT2A 1556/4885GBA1 237/4885

“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.

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