SCHEMBL3792829

SCHEMBL3792829

CC1(C)OCC(CN)CO1

nearest known ligand 0.33

Predicted protein targets (top 3)

geneUniProtsupporting neighboursconfidence
CA2 P00918 2/20 0.33
APP P05067 1/20 0.33
NCF1 P14598 1/20 0.32

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
SCHEMBL13803857 0.76 APP (0.33) CA2APP
SCHEMBL6276420 0.76 APP (0.33) CA2APP
SCHEMBL24230268 0.75
SCHEMBL12744068 0.74 APP (0.33) APP
SCHEMBL19011946 0.74 APP (0.33) APP
SCHEMBL23671782 0.74 APP (0.33) APP
SCHEMBL714032 0.74 CA2 (0.33) CA2APP
SCHEMBL75036 0.74 APLNR (0.35) APP
SCHEMBL3827605 0.74 APP (0.33) APP
SCHEMBL8833046 0.74 APP (0.33) APP

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-12570648-B2 6,7-dihydro-5H-pyrido[2,3-c]pyridazine derivatives and related compounds as Bcl-xL protein inhibitors and pro-apoptotic agents for treating cancer LES LABORATOIRES SERVIER (FR) 2026-03-10 US disclosed
US-20260027220-A1 EPHA2 BCL-XL INHIBITOR ANTIBODY-DRUG CONJUGATES AND METHODS OF USE THEREOF NOVARTIS AG (CH) 2026-01-29 US disclosed
US-20250339547-A1 MET BCL-XL INHIBITOR ANTIBODY-DRUG CONJUGATES AND METHODS OF USE THEREOF NOVARTIS AG (CH) 2025-11-06 US disclosed
EP-4525926-A1 MET BCL-XL INHIBITOR ANTIBODY-DRUG CONJUGATES AND METHODS OF USE THEREOF Novartis AG (CH) 2025-03-26 EP disclosed
EP-4525925-A1 EPHA2 BCL-XL INHIBITOR ANTIBODY-DRUG CONJUGATES AND METHODS OF USE THEREOF Novartis AG (CH) 2025-03-26 EP disclosed
CN-113923988-B Substituted arylmethyl ureas and heteroarylmethyl ureas, analogs thereof, and methods of using the same 爱彼特生物制药公司 2024-12-13 CN disclosed
EP-4455159-A1 GASTRIC INHIBITORY PEPTIDE RECEPTOR LIGANDS WITH BIO-DISTRIBUTION MODIFIER 3B Pharmaceuticals GmbH (DE) 2024-10-30 EP disclosed
US-20240269304-A1 BCL-XL INHIBITOR ANTIBODY-DRUG CONJUGATES AND METHODS OF USE THEREOF LES LABORATOIRES SERVIER (FR) 2024-08-15 US disclosed
CN-114450284-B 6, 7-Dihydro-5H-pyrido [2,3-C ] pyridazine derivatives as BCL-XL protein inhibitors 法国施维雅药厂 2024-05-07 CN disclosed
EP-3893645-B1 SUBSTITUTED ARYLMETHYLUREAS AND HETEROARYLMETHYLUREAS, ANALOGUES THEREOF, AND METHODS USING SAME ARBUTUS BIOPHARMA CORP (CA) 2024-04-17 EP disclosed
EP-3638716-A1 POLY(PHOSPHOESTERS) FOR DELIVERY OF NUCLEIC ACIDS Translate Bio, Inc. (US) 2020-04-22 EP disclosed
WO-2018231709-A1 POLY(PHOSPHOESTERS) FOR DELIVERY OF NUCLEIC ACIDS TRANSLATE BIO, INC. (US) 2018-12-20 WO disclosed
CN-107922394-A 3 tetrazole radical benzene, 1,2 disulfonic acid amide derivative as metal beta lactamase restrainer 默沙东公司 2018-04-17 CN disclosed
US-20170190729-A1 POLYENE MACROLIDE DERIVATIVE SHIONOGI & CO., LTD. (JP) 2017-07-06 US disclosed
US-20150148543-A1 Methods and Compositions for the Synthesis of Multimerizing Agents TAKEDA PHARMACEUTICAL COMPANY LIMITED (JP) 2015-05-28 US disclosed
US-9024028-B2 Methods and compositions for the synthesis of multimerizing agents ARIAD PHARMACEUTICALS, INC. (US) 2015-05-05 US disclosed
US-20140171649-A1 Methods and Compositions for the Synthesis of Multimerizing Agents ARIAD PHARMACEUTICALS, INC. (US) 2014-06-19 US disclosed
WO-2010081731-A2 DERIVATIVES OF SYRINGOLIN A Max-Planck-Gesellschaft zur Förderung der Wissenschaften e.V (DE) 2010-07-22 WO disclosed
WO-2010081731-A2 DERIVATIVES OF SYRINGOLIN A Max-Planck-Gesellschaft zur Förderung der Wissenschaften e.V (DE) 2010-07-22 WO disclosed
US-20090076062-A1 Organic Compounds MAIBAUM JUERGEN KLAUS 2009-03-19 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 (8 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-20140171649-A1 Methods and Compositions for the Synthesis of Multimerizing Agents PIP5K1C, PIP4K2C, IPMK CA2 543/4885APP 3210/4885NCF1 616/4885
US-20170190729-A1 POLYENE MACROLIDE DERIVATIVE ERG28, RPL23, RPL10 CA2 4408/4885APP 3032/4885NCF1 4028/4885
US-20260027220-A1 EPHA2 BCL-XL INHIBITOR ANTIBODY-DRUG CONJUGATES AND METHODS OF USE THEREOF EPHA2, EPHA1, EPHB1 CA2 1668/4885APP 2647/4885NCF1 1654/4885
US-20250339547-A1 MET BCL-XL INHIBITOR ANTIBODY-DRUG CONJUGATES AND METHODS OF USE THEREOF MET, BCL3, BCL9 CA2 3647/4885APP 3104/4885NCF1 2226/4885
US-20150148543-A1 Methods and Compositions for the Synthesis of Multimerizing Agents PARG, POLI, MCM6 CA2 933/4885APP 1098/4885NCF1 805/4885
US-12570648-B2 6,7-dihydro-5H-pyrido[2,3-c]pyridazine derivatives and related compounds as Bcl-xL protein inhibitors and pro-apoptotic agents for treating cancer BCOR, BCL2A1, BAK1 CA2 2981/4885APP 2733/4885NCF1 705/4885
US-20240269304-A1 BCL-XL INHIBITOR ANTIBODY-DRUG CONJUGATES AND METHODS OF USE THEREOF BCL3, BCL9, BCL2L10 CA2 4016/4885APP 3514/4885NCF1 1488/4885
US-20090076062-A1 Organic Compounds AGTR1, AGTR2, REN CA2 1571/4885APP 84/4885NCF1 2990/4885

“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.