SCHEMBL4571091

SCHEMBL4571091

COC(=O)[C@@H]1CSCCN1

nearest known ligand 0.43

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
KMT2A Q03164 1/20 0.41
CHRNB2 P17787 2/20 0.33
CHRNA4 P43681 2/20 0.33
CHRNB4 P30926 1/20 0.33
CHRNA3 P32297 1/20 0.33
CHRNA7 P36544 1/20 0.33
KDM4E B2RXH2 1/20 0.32
ALDH1A1 P00352 1/20 0.32
CYP1A2 P05177 1/20 0.32
GAA P10253 1/20 0.32
CYP2D6 P10635 1/20 0.32
MAPT P10636 1/20 0.32
CYP2C9 P11712 1/20 0.32
HPGD P15428 1/20 0.32
ALOX15 P16050 1/20 0.32
CYP2C19 P33261 1/20 0.32
HSD17B10 Q99714 1/20 0.32
DPP4 P27487 1/20 0.31
DPP8 Q6V1X1 1/20 0.31
DPP9 Q86TI2 1/20 0.31

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
SCHEMBL2675696 1.00 KMT2A (0.41) KMT2ACHRNB2CHRNA4CHRNB4CHRNA3
SCHEMBL5493487 1.00 KMT2A (0.41) KMT2ACHRNB2CHRNA4CHRNB4CHRNA3
Hydrochloric Acid SCHEMBL2675695 0.98 KMT2A (0.40) KMT2ACHRNB2CHRNA4CHRNB4CHRNA3
Hydrochloric Acid SCHEMBL5362921 0.98 KMT2A (0.40) KMT2ACHRNB2CHRNA4CHRNB4CHRNA3
SCHEMBL5224314 0.82
SCHEMBL3361966 0.82
SCHEMBL11122946 0.82
Hydrochloric Acid SCHEMBL201248 0.80 KMT2A (0.41) KMT2ACHRNB2CHRNA4CHRNB4CHRNA3
Hydrochloric Acid SCHEMBL201249 0.80 KMT2A (0.41) KMT2ACHRNB2CHRNA4CHRNB4CHRNA3
Hydrochloric Acid SCHEMBL7350919 0.80 KMT2A (0.41) KMT2ACHRNB2CHRNA4CHRNB4CHRNA3

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20250084044-A1 PROTOPORPHYRINOGEN OXIDASE INHIBITORS ENKO CHEM, INC. (US) 2025-03-13 US disclosed
EP-4462999-A1 PROTOPORPHYRINOGEN OXIDASE INHIBITORS Enko Chem, Inc. (US) 2024-11-20 EP disclosed
CN-118541030-A Protoporphyrinogen oxidase inhibitors 恩科化学公司 2024-08-23 CN disclosed
WO-2023137307-A1 PROTOPORPHYRINOGEN OXIDASE INHIBITORS ENKO CHEM, INC. (US) 2023-07-20 WO disclosed
EP-2130825-B1 N-SUBSTITUTED THIOMORPHOLINE DERIVATIVES AS THE INHIBITORS OF DIPEPTIDYL PEPTIDASE IV AND THE PHARMACEUTICAL USES THEREOF BEIJING MOLECULE SCIENCE AND TECHNOLOGY CO LTD (CN) 2014-08-06 EP disclosed
US-8173643-B2 N-substituted thiomorpholine derivatives as the inhibitors of dipeptidyl peptidase IV and the pharmaceutical uses thereof BEIJING MOLECULE SCIENCE AND TECHNOLOGY CO., LTD. (CN) 2012-05-08 US disclosed
US-8173643-B2 N-substituted thiomorpholine derivatives as the inhibitors of dipeptidyl peptidase IV and the pharmaceutical uses thereof BEIJING MOLECULE SCIENCE AND TECHNOLOGY CO., LTD. (CN) 2012-05-08 US disclosed
US-20100113433-A1 N-Substituted Thiomorpholine Derivatives as the Inhibitors of Dipeptidyl Peptidase IV and the Pharmaceutical Uses Thereof BEIJING MOLECULE SCIENCE AND TECHNOLOGY CO., LTD. (CN) 2010-05-06 US disclosed
US-20100113433-A1 N-Substituted Thiomorpholine Derivatives as the Inhibitors of Dipeptidyl Peptidase IV and the Pharmaceutical Uses Thereof BEIJING MOLECULE SCIENCE AND TECHNOLOGY CO., LTD. (CN) 2010-05-06 US disclosed
EP-2130825-A1 N-SUBSTITUTED THIOMORPHOLINE DERIVATIVES AS THE INHIBITORS OF DIPEPTIDYL PEPTIDASE IV AND THE PHARMACEUTICAL USES THEREOF Beijing Molecule Science and Technology Co., Ltd. (CN) 2009-12-09 EP disclosed
US-7304057-B2 Substituted 6-membered N-heterocyclic compounds and method for their use as neurological regulator Institute of Pharmacology and Toxicology Accademy of Military Medical Sciences P.L.A. China (CN) 2007-12-04 US disclosed
US-7304057-B2 Substituted 6-membered N-heterocyclic compounds and method for their use as neurological regulator Institute of Pharmacology and Toxicology Accademy of Military Medical Sciences P.L.A. China (CN) 2007-12-04 US disclosed
US-7304057-B2 Substituted 6-membered N-heterocyclic compounds and method for their use as neurological regulator Institute of Pharmacology and Toxicology Accademy of Military Medical Sciences P.L.A. China (CN) 2007-12-04 US disclosed
US-20050130958-A1 Substituted 6−membered n−heterocyclic compounds and their uses as neurological regulator INSTITUTE OF PHARMACOLOGY AND TOXICOLOGY ACADEMY OF MILITARY MEDICAL SCIENCES P.L.A. CHINA (CN) 2005-06-16 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 (3 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-20250084044-A1 PROTOPORPHYRINOGEN OXIDASE INHIBITORS PPOX, CYP4X1, PNPO KMT2A 4160/4885CHRNB2 4802/4885CHRNA4 4759/4885
US-20100113433-A1 N-Substituted Thiomorpholine Derivatives as the Inhibitors of Dipeptidyl Peptidase IV and the Pharmaceutical Uses Thereof DPP4, DPP3, DPP7 KMT2A 4115/4885CHRNB2 2893/4885CHRNA4 1554/4885
US-20050130958-A1 Substituted 6−membered n−heterocyclic compounds and their uses as neurological regulator BDNF, NGF, NTRK2 KMT2A 3699/4885CHRNB2 299/4885CHRNA4 474/4885

“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.