SCHEMBL91191

SCHEMBL91191

CCCc1csc2ccccc12

nearest known ligand 0.62

Predicted protein targets (top 18)

geneUniProtsupporting neighboursconfidence
CYP2A6 P11509 3/20 0.62
IDO1 P14902 1/20 0.53
ALDH1A1 P00352 1/20 0.50
CHRNA7 P36544 1/20 0.49
SMN1; SMN2 Q16637 4/20 0.47
CRHBP P24387 1/20 0.47
CRHR2 Q13324 1/20 0.47
CA1 P00915 1/20 0.47
CA2 P00918 1/20 0.47
MAPT P10636 1/20 0.46
MTNR1A P48039 1/20 0.46
DRD2 P14416 2/20 0.45
SLC6A4 P31645 1/20 0.45
TP53 P04637 2/20 0.44
RXFP1 Q9HBX9 1/20 0.44
TAAR1 Q96RJ0 1/20 0.42
DRD4 P21917 1/20 0.42
DRD3 P35462 1/20 0.42

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
SCHEMBL3789614 0.89 CYP2A6 (0.58) CYP2A6IDO1ALDH1A1CHRNA7SMN1; SMN2
SCHEMBL368354 0.87 CYP2A6 (0.56) CYP2A6IDO1ALDH1A1CHRNA7SMN1; SMN2
SCHEMBL9347729 0.85 CYP2A6 (0.55) CYP2A6IDO1ALDH1A1CHRNA7SMN1; SMN2
SCHEMBL9347766 0.85 CYP2A6 (0.55) CYP2A6IDO1ALDH1A1CHRNA7SMN1; SMN2
SCHEMBL8870175 0.84 IDO1 (0.57) CYP2A6IDO1ALDH1A1CHRNA7SMN1; SMN2
SCHEMBL91157 0.83 CYP2A6 (0.67) CYP2A6IDO1ALDH1A1CHRNA7SMN1; SMN2
SCHEMBL25029575 0.81 CYP2A6 (0.50) CYP2A6IDO1ALDH1A1CHRNA7SMN1; SMN2
SCHEMBL25029850 0.80 ALDH1A1 (0.58) CYP2A6IDO1ALDH1A1CHRNA7SMN1; SMN2
SCHEMBL1304400 0.80 CYP2A6 (0.62) CYP2A6IDO1ALDH1A1CHRNA7SMN1; SMN2
SCHEMBL7845291 0.80 CYP2A6 (0.62) CYP2A6IDO1ALDH1A1CHRNA7SMN1; SMN2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2021163727-A1 PIKFYVE KINASE INHIBITORS AcuraStem Incorporated (US) 2021-08-19 WO disclosed
US-20170114054-A1 SUBSTITUTED PYRIDINONES AS MGAT2 INHIBITORS BRISTOL MYERS SQUIBB CO (US) 2017-04-27 US disclosed
US-20150368262-A1 ALPHA HELIX MIMETICS AND METHODS RELATING THERETO Prism BioLab Co., Ltd. (JP) 2015-12-24 US disclosed
US-9040531-B2 Alpha helix mimetics and methods relating thereto Prism BioLab Co., Ltd. (JP) 2015-05-26 US disclosed
EP-1919492-B1 GROWTH HORMONE SECRETAGOGUES IPSEN PHARMA (FR) 2013-03-06 EP disclosed
US-20130030008-A1 ACYLAMINO-SUBSTITUTED FUSED CYCLOPENTANECARBOXYLIC ACID DERIVATIVES AND THEIR USE AS PHARMACEUTICALS SANOFI (FR) 2013-01-31 US disclosed
US-8362073-B2 Acylamino-substituted fused cyclopentanecarboxylic acid derivatives and their use as pharmaceuticals SANOFI (FR) 2013-01-29 US disclosed
US-20120226066-A1 PROCESSES FOR INTERMEDIATES FOR MACROCYCLIC COMPOUNDS MARSAULT ERIC (CA) 2012-09-06 US disclosed
US-20120226072-A1 PROCESSES FOR INTERMEDIATES FOR MACROCYCLIC COMPOUNDS MARSAULT ERIC (CA) 2012-09-06 US disclosed
US-20120226067-A1 PROCESSES FOR INTERMEDIATES FOR MACROCYCLIC COMPOUNDS MARSAULT ERIC (CA) 2012-09-06 US disclosed
US-20090240027-A1 INTERMEDIATES FOR MACROCYCLIC COMPOUNDS TRANZYME PHARMA INC. 2009-09-24 US disclosed
US-20090192138-A1 COMPOUNDS BAESCHLIN DANIEL KASPAR 2009-07-30 US disclosed
US-20090137835-A1 PROCESSES FOR INTERMEDIATES FOR MACROCYCLIC COMPOUNDS TRANZYME PHARMA INC. 2009-05-28 US disclosed
US-7521420-B2 Macrocyclic antagonists of the motilin receptor TRANZYME PHARMA, INC. (CA) 2009-04-21 US disclosed
WO-2007071738-A1 CONDENSED HETEROCYCLIC COMPOUNDS USEFUL AS DPP-IV INHIBITORS NOVARTIS AG (CH) 2007-06-28 WO disclosed
WO-2007061360-A2 NOVEL 3-BICYCLOCARBONYLAMINOPYRIDINE-2-CARBOXAMIDES OR 3-BICYCLOCARBONYLAMINOPYRAZINE-2-CARBOXAMIDES ASTRAZENECA AB (SE) 2007-05-31 WO disclosed
WO-2007014258-A2 GROWTH HORMONE SECRETAGOGUES SOCIETE DE CONSEILS DE RECHERCHES ET D'APPLICATIONS SCIENTIFIQUES S.A.S. (FR) 2007-02-01 WO disclosed
US-20060052509-A1 Composition containing carbon nanotubes having coating thereof and process for producing them MITSUBISHI RAYON CO., LTD. (JP) 2006-03-09 US disclosed
CN-1144791-C Triazole compounds and use thereof as dopamine-D3-ligands BASF 2004-04-07 CN disclosed
WO-2001007431-A2 BENZOTHIOPHENE DERIVATIVES ELI LILLY AND COMPANY (US) 2001-02-01 WO 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 (9 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-20090137835-A1 PROCESSES FOR INTERMEDIATES FOR MACROCYCLIC COMPOUNDS MLNR, CHRM2, CHRM1 CYP2A6 1454/4885IDO1 3504/4885ALDH1A1 2978/4885
US-20150368262-A1 ALPHA HELIX MIMETICS AND METHODS RELATING THERETO PLOD3, COL1A1, THPO CYP2A6 2913/4885IDO1 2687/4885ALDH1A1 1511/4885
US-20170114054-A1 SUBSTITUTED PYRIDINONES AS MGAT2 INHIBITORS PLAAT2, ACAT2, MGAT2 CYP2A6 302/4885IDO1 801/4885ALDH1A1 534/4885
US-20120226066-A1 PROCESSES FOR INTERMEDIATES FOR MACROCYCLIC COMPOUNDS MLNR, CHRM2, CHRM1 CYP2A6 1454/4885IDO1 3504/4885ALDH1A1 2978/4885
US-20090192138-A1 COMPOUNDS DPP4, DPP3, DPP8 CYP2A6 836/4885IDO1 702/4885ALDH1A1 363/4885
US-20090240027-A1 INTERMEDIATES FOR MACROCYCLIC COMPOUNDS MLNR, CCKAR, CHRM2 CYP2A6 1985/4885IDO1 3207/4885ALDH1A1 2729/4885
US-20120226067-A1 PROCESSES FOR INTERMEDIATES FOR MACROCYCLIC COMPOUNDS MLNR, CHRM2, CCKAR CYP2A6 1527/4885IDO1 3184/4885ALDH1A1 3005/4885
US-20130030008-A1 ACYLAMINO-SUBSTITUTED FUSED CYCLOPENTANECARBOXYLIC ACID DERIVATIVES AND THEIR USE AS PHARMACEUTICALS EDF1, LPAR2, LIPG CYP2A6 2339/4885IDO1 1180/4885ALDH1A1 2149/4885
US-20120226072-A1 PROCESSES FOR INTERMEDIATES FOR MACROCYCLIC COMPOUNDS MLNR, CHRM2, CHRM1 CYP2A6 1454/4885IDO1 3504/4885ALDH1A1 2978/4885

“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.