SCHEMBL178287

SCHEMBL178287

CCC1CCN(CC)CC1

nearest known ligand 0.47

Predicted protein targets (top 8)

geneUniProtsupporting neighboursconfidence
SMN1; SMN2 Q16637 1/20 0.46
HRH3 Q9Y5N1 3/20 0.43
EPHX1 P07099 2/20 0.40
EPHX2 P34913 1/20 0.38
HSD11B1 P28845 2/20 0.36
KMT2A Q03164 1/20 0.34
NCF1 P14598 1/20 0.33
ACHE P22303 1/20 0.33

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
Butane SCHEMBL21084742 0.93 SMN1; SMN2 (0.42) SMN1; SMN2HRH3EPHX1EPHX2HSD11B1
Butane SCHEMBL21084740 0.93 SMN1; SMN2 (0.42) SMN1; SMN2HRH3EPHX1EPHX2HSD11B1
SCHEMBL2759515 0.91 SMN1; SMN2 (0.41) SMN1; SMN2HRH3EPHX1EPHX2HSD11B1
SCHEMBL24671546 0.91 ACHE (0.47) SMN1; SMN2HRH3EPHX1ACHE
SCHEMBL26480956 0.91 SMN1; SMN2 (0.41) SMN1; SMN2HRH3EPHX1EPHX2HSD11B1
SCHEMBL6672852 0.87 SMN1; SMN2 (0.38) SMN1; SMN2HRH3EPHX1EPHX2HSD11B1
SCHEMBL25856473 0.87 KMT2A (0.46) SMN1; SMN2HRH3KMT2AACHE
SCHEMBL13179250 0.85 SMN1; SMN2 (0.41) SMN1; SMN2HRH3EPHX1HSD11B1
SCHEMBL12717977 0.84
SCHEMBL12717971 0.84

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-111629828-B Aluminosilicate zeolite UZM-50 环球油品有限责任公司 2023-07-21 CN claimed
WO-2024112692-A1 CASITAS B-LINEAGE LYMPHOMA PROTOONCOGENE B (CBL-B) DEGRADING COMPOUNDS AND ASSOCIATED METHODS OF USE ARVINAS OPERATIONS, INC. (US) 2024-05-30 WO disclosed
US-20240067642-A1 COMPOUNDS AND USES THEREOF FOGHORN THERAPEUTICS INC. 2024-02-29 US disclosed
US-11857519-B2 Compounds and methods for the targeted degradation of enhancer of zeste homolog 2 polypeptide ARVINAS OPERATIONS, INC. (US) 2024-01-02 US disclosed
US-11833208-B2 PLK1 selective degradation inducing compound UPPTHERA, INC. (KR) 2023-12-05 US disclosed
US-20230372498-A1 PLK1 SELECTIVE DEGRADATION INDUCING COMPOUND UPPTHERA (KR) 2023-11-23 US disclosed
EP-3628044-B1 PYRROLO[2,3-C]PYRIDINES AND RELATED ANALOGS AS LSD-1 INHIBITORS UNIV MICHIGAN REGENTS (US) 2023-11-22 EP disclosed
US-20230357249-A1 ANDROGEN RECEPTOR PROTEIN DEGRADERS WITH A TRICYCLIC CEREBLON LIGAND UNIV MICHIGAN REGENTS (US) 2023-11-09 US disclosed
WO-2023215482-A1 TETRAHYDROISOQUINOLINE HETEROBIFUNCTIONAL BCL-XL DEGRADERS Treeline Biosciences, Inc. (US) 2023-11-09 WO disclosed
US-20230357249-A1 ANDROGEN RECEPTOR PROTEIN DEGRADERS WITH A TRICYCLIC CEREBLON LIGAND UNIV MICHIGAN REGENTS (US) 2023-11-09 US disclosed
US-20070270473-A1 Sulfonamide Compounds and Uses Thereof ELIXIR PHARMACEUTICALS, INC. 2007-11-22 US disclosed
US-20070249649-A1 INHIBITORS OF C-FMS KINASE JANSSEN PHARMACEUTICA, N.V. (BE) 2007-10-25 US disclosed
US-20070249685-A1 4-Cyano-1H-imidazole-2-carboxylic acid [2-cyclohex-1-enyl-4-(2,6-dioxo-piperidin-4-yl)-phenyl]-amide; tyrosine kinase inhibitor; autoimmune diseases, antiinflammatory, anticarcinogenic agent JANSSEN PHARMACEUTICA, N.V. (BE) 2007-10-25 US disclosed
US-20070249618-A1 Novel Piperidine Derivatives as Histamine H3 Receptor Ligands for Treatment of Depression ASTRAZENECA AB (SE) 2007-10-25 US disclosed
US-20070197537-A1 Heterobicyclic thiophene compounds and methods of use ARRAY BIOPHARMA, INC. 2007-08-23 US disclosed
US-7244441-B2 Stents and intra-luminal prostheses containing map kinase inhibitors SCIOS, INC. (US) 2007-07-17 US disclosed
US-20070123516-A1 Method of treating mucus hypersecretion BOEHRINGER INGELHEIM PHARMA GMBH & CO., KG (DE) 2007-05-31 US disclosed
US-7189739-B2 Compounds and methods to treat cardiac failure and other disorders SCIOS, INC. (US) 2007-03-13 US disclosed
US-20070043078-A1 Angiogenesis inhibitor KOWA CO., LTD. (JP) 2007-02-22 US disclosed
US-20070004742-A1 Arylpiperazinyl compounds EPIX DELAWARE, INC. 2007-01-04 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 (13 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-20070197537-A1 Heterobicyclic thiophene compounds and methods of use ERBB2, LCK, SRC SMN1; SMN2 2264/4885HRH3 945/4885EPHX1 2585/4885
US-20230357249-A1 ANDROGEN RECEPTOR PROTEIN DEGRADERS WITH A TRICYCLIC CEREBLON LIGAND AR, GPER1, CRBN SMN1; SMN2 2044/4885HRH3 4257/4885EPHX1 3664/4885
US-20230372498-A1 PLK1 SELECTIVE DEGRADATION INDUCING COMPOUND PLK1, BUB1B, BUB1 SMN1; SMN2 3348/4885HRH3 3536/4885EPHX1 2442/4885
US-20070249649-A1 INHIBITORS OF C-FMS KINASE FES, MUSK, FRK SMN1; SMN2 2217/4885HRH3 685/4885EPHX1 3409/4885
US-20070043078-A1 Angiogenesis inhibitor FLT4, FLT1, KDR SMN1; SMN2 4206/4885HRH3 633/4885EPHX1 963/4885
US-20070270473-A1 Sulfonamide Compounds and Uses Thereof GHSR, GHRHR, SSTR2 SMN1; SMN2 1606/4885HRH3 1448/4885EPHX1 3138/4885
US-20070249685-A1 4-Cyano-1H-imidazole-2-carboxylic acid [2-cyclohex-1-enyl-4-(2,6-dioxo-piperidin-4-yl)-phenyl]-amide; tyrosine kinase inhibitor; autoimmune diseases, antiinflammatory, anticarcinogenic agent MUSK, CHUK, CAMK4 SMN1; SMN2 1787/4885HRH3 453/4885EPHX1 3255/4885
US-20070249618-A1 Novel Piperidine Derivatives as Histamine H3 Receptor Ligands for Treatment of Depression HRH3, HRH1, HRH4 SMN1; SMN2 4112/4885HRH3 1/4885EPHX1 1212/4885
US-20070123516-A1 Method of treating mucus hypersecretion MUC1, CFTR, MAPKAPK5 SMN1; SMN2 4866/4885HRH3 163/4885EPHX1 1327/4885
US-11857519-B2 Compounds and methods for the targeted degradation of enhancer of zeste homolog 2 polypeptide CRBN, MDM2, VHL SMN1; SMN2 881/4885HRH3 3219/4885EPHX1 2385/4885
US-20070004742-A1 Arylpiperazinyl compounds HTR5A, HTR1A, HTR2A SMN1; SMN2 577/4885HRH3 639/4885EPHX1 354/4885
US-11833208-B2 PLK1 selective degradation inducing compound PLK1, BUB1B, BUB1 SMN1; SMN2 3348/4885HRH3 3536/4885EPHX1 2442/4885
US-20240067642-A1 COMPOUNDS AND USES THEREOF VHL, TFEB, BECN1 SMN1; SMN2 368/4885HRH3 2014/4885EPHX1 1508/4885

“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.