Kenpaullone

Kenpaullone

SCHEMBL79889

O=C1Cc2c([nH]c3ccc(Br)cc23)-c2ccccc2N1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
GSK3B P49841 20/20 1.00
CCNB2 O95067 19/20 1.00
CDK1 P06493 19/20 1.00
CCNB1 P14635 19/20 1.00
CCNB3 Q8WWL7 19/20 1.00
CDK5 Q00535 17/20 1.00
CDK5R1 Q15078 17/20 1.00
CCNA2 P20248 3/20 1.00
CDK2 P24941 3/20 1.00
CCNA1 P78396 3/20 1.00
CCNT1 O60563 2/20 1.00
CDK9 P50750 2/20 1.00
GSK3A P49840 2/20 1.00
KDM4E B2RXH2 1/20 1.00
MEN1 O00255 1/20 1.00
CDC7 O00311 1/20 1.00
PLK4 O00444 1/20 1.00
CHEK1 O14757 1/20 1.00
AURKA O14965 1/20 1.00
NPC1 O15118 1/20 1.00

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
Kenpaullone SCHEMBL30789744 1.00 GSK3B (1.00) GSK3BCCNB2CDK1CCNB1CCNB3
Kenpaullone SCHEMBL29366756 1.00 GSK3B (1.00) GSK3BCCNB2CDK1CCNB1CCNB3
SCHEMBL5688213 0.90 CCNB2 (1.00) GSK3BCCNB2CDK1CCNB1CCNB3
SCHEMBL30319776 0.90 CCNB2 (1.00) GSK3BCCNB2CDK1CCNB1CCNB3
SCHEMBL5688155 0.90 GSK3B (1.00) GSK3BCCNB2CDK1CCNB1CCNB3
SCHEMBL30319757 0.90 GSK3B (1.00) GSK3BCCNB2CDK1CCNB1CCNB3
SCHEMBL5689156 0.86 GSK3B (1.00) GSK3BCCNB2CDK1CCNB1CCNB3
SCHEMBL30319766 0.86 GSK3B (1.00) GSK3BCCNB2CDK1CCNB1CCNB3
Paullone SCHEMBL3178594 0.85 CCNB2 (1.00) GSK3BCCNB2CDK1CCNB1CCNB3
Paullone SCHEMBL29407267 0.85 CCNB2 (1.00) GSK3BCCNB2CDK1CCNB1CCNB3

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-RE50313-E1 Musculoskeletal stem cell and medium for inducing differentiation of musculoskeletal stem cell CELLATOZ THERAPEUTICS, INC. (KR) 2025-02-25 US claimed
US-20240269129-A1 GLYCOGEN SYNTHASE KINASE 3 (GSK3) INHIBITORS FOR TREATING CTNNB1 SYNDROME THE BROAD INSTITUTE, INC. 2024-08-15 US claimed
US-20240091254-A1 WNT AGONISTS FOR PREVENTION OF CANCER Stichting Amsterdam UMC (NL) 2024-03-21 US claimed
CN-116438295-A Methods and compositions for culturing pluripotent cell suspensions 生命技术公司 2023-07-14 CN claimed
EP-4168536-A1 METHODS AND COMPOSITIONS FOR CULTIVATING PLURIPOTENT CELL SUSPENSIONS Life Technologies Corporation (US) 2023-04-26 EP claimed
EP-3702445-B1 NOVEL MUSCULOSKELETAL STEM CELL CELLATOZ THERAPEUTICS INC (KR) 2022-12-07 EP claimed
US-20220281930-A1 COMPOSITIONS AND METHODS FOR THE TREATMENT OF PATHOLOGICAL PAIN AND ITCH DUKE UNIVERSITY (US) 2022-09-08 US claimed
EP-4017873-A2 COMPOSITIONS AND METHODS FOR THE TREATMENT OF PATHOLOGICAL PAIN AND ITCH Duke University (US) 2022-06-29 EP claimed
US-20210395698-A1 METHODS AND COMPOSITIONS FOR CULTIVATING PLURIPOTENT CELL SUSPENSIONS Life Technologies Corporation 2021-12-23 US claimed
US-20200399602-A1 Method for Differentiation of Human Pluripotent Stem Cell Lines in Suspension Culture AGENCY FOR SCIENCE, TECHNOLOGY AND RESEARCH (SG) 2020-12-24 US claimed
WO-2013142817-A2 COMPOSITIONS AND METHODS TO IMPROVE THE THERAPEUTIC BENEFIT OF INDIRUBIN AND ANALOGS THEREOF, INCLUDING MEISOINDIGO BROWN DENNIS (US) 2013-09-26 WO claimed
US-20130236436-A1 EXPANDABLE CELL SOURCE OF NEURONAL STEM CELL POPULATIONS AND METHODS FOR OBTAINING AND USNIG THEM ZHANG KANG (US) 2013-09-12 US claimed
US-20130095567-A1 DIRECTED DIFFERENTIATION AND MATURATION OF PLURIPOTENT CELLS INTO HEPATOCYTE LIKE CELLS BY MODULATION OF WNT-SIGNALLING PATHWAY CELLARTIS AB (SE) 2013-04-18 US claimed
EP-2550355-A1 DIRECTED DIFFERENTIATION AND MATURATION OF PLURIPOTENT CELLS INTO HEPATOCYTE LIKE CELLS BY MODULATION OF WNT-SIGNALLING PATHWAY Cellartis AB (SE) 2013-01-30 EP claimed
EP-2494865-A2 GUT FLORA-DERIVED EXTRACELLULAR VESICLES, AND METHOD FOR SEARCHING FOR A DISEASE MODEL, VACCINE, AND CANDIDATE DRUG AND FOR DIAGNOSIS USING SAME Aeon Medix Inc. (KR) 2012-09-05 EP claimed
WO-2012034101-A2 EXPANDABLE CELL SOURCE OF NEURONAL STEM CELL POPULATIONS AND METHODS FOR OBTAINING AND USING THEM THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 2012-03-15 WO claimed
WO-2011116930-A1 DIRECTED DIFFERENTIATION AND MATURATION OF PLURIPOTENT CELLS INTO HEPATOCYTE LIKE CELLS BY MODULATION OF WNT-SIGNALLING PATHWAY CELLARTIS AB (SE) 2011-09-29 WO claimed
US-20060217368-A1 Drug for nerve regeneration KYOWA HAKKO KOGYO CO., LTD. (JP) 2006-09-28 US claimed
EP-1645286-A1 DRUG FOR NERVE REGENERATION KYOWA HAKKO KOGYO CO., LTD. (JP) 2006-04-12 EP claimed
US-20020042412-A1 Fused azepinone cyclin dependent kinase inhibitors HEALTH AND HUMAN SERVICES, DEPARTMENT OF, GOVERNMENT OF THE UNITED STATES OF AMERICA AS REPRESENTED BY THE SECRETARY OF THE, THE 2002-04-11 US claimed

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-20060217368-A1 Drug for nerve regeneration GSK3A, BDNF, GSK3B GSK3B 3/4885CCNB2 2747/4885CDK1 435/4885
US-20240269129-A1 GLYCOGEN SYNTHASE KINASE 3 (GSK3) INHIBITORS FOR TREATING CTNNB1 SYNDROME GSK3B, GSK3A, CTNNB1 GSK3B 1/4885CCNB2 1365/4885CDK1 296/4885
US-20020042412-A1 Fused azepinone cyclin dependent kinase inhibitors CCNI, CCNK, CDKN1A GSK3B 4154/4885CCNB2 61/4885CDK1 13/4885

“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.