SCHEMBL11246

SCHEMBL11246

COc1cc(Br)ccc1CCO

nearest known ligand 0.69

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
PYCR1 P32322 1/20 0.49
KDM4E B2RXH2 2/20 0.44
TDP1 Q9NUW8 2/20 0.44
ERN1 O75460 1/20 0.42
MEN1 O00255 1/20 0.42
USP2 O75604 1/20 0.42
ALDH1A1 P00352 1/20 0.42
GAA P10253 1/20 0.42
MAPT P10636 1/20 0.42
THRB P10828 1/20 0.42
ALOX15 P16050 1/20 0.42
CASP1 P29466 1/20 0.42
HTT P42858 1/20 0.42
RECQL P46063 1/20 0.42
BLM P54132 1/20 0.42
KMT2A Q03164 1/20 0.42
HSD17B10 Q99714 1/20 0.42
L3MBTL1 Q9Y468 1/20 0.42
HTR2A P28223 2/20 0.40
HTR2C P28335 1/20 0.40

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
SCHEMBL29937640 1.00 PYCR1 (0.49) PYCR1KDM4ETDP1ERN1MEN1
SCHEMBL6044488 0.85 KDM4E (0.53) KDM4ETDP1MEN1USP2ALDH1A1
SCHEMBL30223764 0.85 PYCR1 (0.51) PYCR1KDM4ETDP1MEN1USP2
SCHEMBL1427602 0.85 PYCR1 (0.51) PYCR1KDM4ETDP1MEN1USP2
SCHEMBL3484619 0.83 PYCR1 (0.50) PYCR1KDM4ETDP1HTR2A
SCHEMBL3858881 0.82 TSHR (0.46) TDP1MEN1ALDH1A1GAAMAPT
SCHEMBL1569750 0.81 TAAR1 (0.61) HTR2AHTR2CTAAR1
SCHEMBL27488871 0.81 PYCR1 (0.49) PYCR1KDM4ETDP1MEN1USP2
SCHEMBL1446144 0.80 PYCR1 (0.48) PYCR1KDM4ETDP1HTR2A
SCHEMBL20562481 0.80 POLB (0.53) PYCR1KDM4ETDP1MEN1ALDH1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-12503452-B2 Antimicrobial compounds and methods CURZA GLOBAL, LLC (US) 2025-12-23 US disclosed
US-20250213700-A1 COMPOUNDS, COMPOSITIONS, AND METHODS FOR CELL-SPECIFIC PHARMACOLOGY FOX CHASE CHEMICAL DIVERSITY CENTER, INC. 2025-07-03 US disclosed
CN-113574058-B Indole macrocyclic derivative, preparation method and medical application thereof 江苏恒瑞医药股份有限公司 2024-04-16 CN disclosed
WO-2023225369-A1 COMPOUNDS, COMPOSITIONS, AND METHODS FOR CELL-SPECIFIC PHARMACOLOGY DUKE UNIVERSITY (US) 2023-11-23 WO disclosed
WO-2023225369-A1 COMPOUNDS, COMPOSITIONS, AND METHODS FOR CELL-SPECIFIC PHARMACOLOGY DUKE UNIVERSITY (US) 2023-11-23 WO disclosed
US-20230159491-A1 Antimicrobial Compounds and Methods NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT 2023-05-25 US disclosed
US-20230072397-A1 Antimicrobial Compounds and Methods NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT 2023-03-09 US disclosed
US-20220041623-A1 INDOLE MACROCYCLIC DERIVATIVE, PREPARATION METHOD THEREOF AND APPLICATION THEREOF IN MEDICINE JIANGSU HENGRUI MEDICINE CO., LTD. (CN) 2022-02-10 US disclosed
CN-113924292-A Antimicrobial compounds and methods 库扎环球有限责任公司 2022-01-11 CN disclosed
CN-113825748-A Antimicrobial compounds and methods 库扎环球有限责任公司 2021-12-21 CN disclosed
US-20130197217-A1 1, 2, 4-TRIAZOLONE DERIVATIVE TAISHO PHARMACEUTICAL CO., LTD (JP) 2013-08-01 US disclosed
US-20120202777-A1 C-Linked Hydroxamic Acid Derivatives Useful As Antibacterial Agents BROWN MATTHEW FRANK (US) 2012-08-09 US disclosed
US-20120202777-A1 C-Linked Hydroxamic Acid Derivatives Useful As Antibacterial Agents BROWN MATTHEW FRANK (US) 2012-08-09 US disclosed
US-20120202777-A1 C-Linked Hydroxamic Acid Derivatives Useful As Antibacterial Agents BROWN MATTHEW FRANK (US) 2012-08-09 US disclosed
WO-2011045703-A2 C-LINKED HYDROXAMIC ACID DERIVATIVES USEFUL AS ANTIBACTERIAL AGENTS PFIZER INC. (US) 2011-04-21 WO disclosed
WO-2008079836-A2 MACROCYCLIC FACTOR VIIA INHIBITORS USEFUL AS ANTICOAGULANTS BRISTOL-MYERS SQUIBB COMPANY (US) 2008-07-03 WO disclosed
CN-1173974-C Piperidylaminomethyltrifluoromethyl cyclic ether compound as p substance antagonist ������ҩ�����޹�˾ 2004-11-03 CN disclosed
CN-1140525-C 1-trifluoromethyl-4-hydroxy-7-piperidinyl-aminomethylchroman derivatives �Ʒ� 2004-03-03 CN disclosed
CN-1355799-A 1-trifluoromethyl-4-hydroxy-7-piperidinyl-aminomethylchroman derivatives PFIZER PROD INC (US) 2002-06-26 CN disclosed
CN-1279681-A Piperidinylaminomethyltrifluoromethyl cyclic ether compounds as substance P antagonists PFIZER (US) 2001-01-10 CN 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-20230159491-A1 Antimicrobial Compounds and Methods MPO, NISCH, RPN2 PYCR1 2907/4885KDM4E 3027/4885TDP1 4219/4885
US-20120202777-A1 C-Linked Hydroxamic Acid Derivatives Useful As Antibacterial Agents HAX1, LPXN, AGXT PYCR1 1015/4885KDM4E 1331/4885TDP1 2637/4885
US-20130197217-A1 1, 2, 4-TRIAZOLONE DERIVATIVE AVPR1B, AVPR1A, AVPR2 PYCR1 602/4885KDM4E 2260/4885TDP1 707/4885
US-20250213700-A1 COMPOUNDS, COMPOSITIONS, AND METHODS FOR CELL-SPECIFIC PHARMACOLOGY DDT, ABCG2, CES2 PYCR1 1574/4885KDM4E 2188/4885TDP1 1046/4885
US-20230072397-A1 Antimicrobial Compounds and Methods MPO, NISCH, RPN2 PYCR1 2907/4885KDM4E 3027/4885TDP1 4219/4885
US-20220041623-A1 INDOLE MACROCYCLIC DERIVATIVE, PREPARATION METHOD THEREOF AND APPLICATION THEREOF IN MEDICINE MCL1, IDO1, TPH1 PYCR1 187/4885KDM4E 1996/4885TDP1 2045/4885
US-12503452-B2 Antimicrobial compounds and methods MPO, NISCH, RPN2 PYCR1 2907/4885KDM4E 3027/4885TDP1 4219/4885

“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.