SCHEMBL10652

SCHEMBL10652

CC(C)NC(=O)OC(C)(C)C

nearest known ligand 0.57

Predicted protein targets (top 15)

geneUniProtsupporting neighboursconfidence
CA1 P00915 1/20 0.57
CA2 P00918 1/20 0.57
CA7 P43166 1/20 0.57
CTSK P43235 11/20 0.53
CYP2D6 P10635 1/20 0.50
CTSS P25774 4/20 0.47
CTSL P07711 2/20 0.45
CTSB P07858 2/20 0.45
KMT2A Q03164 2/20 0.44
CA12 O43570 1/20 0.43
CA14 Q9ULX7 1/20 0.43
TSHR P16473 1/20 0.42
HSD17B10 Q99714 1/20 0.42
MEN1 O00255 1/20 0.41
GAA P10253 1/20 0.41

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
Ammonia Solution, Strong SCHEMBL9235390 0.98 CA1 (0.55) CA1CA2CA7CTSKCYP2D6
SCHEMBL4821105 0.91 CA1 (0.50) CA1CA2CA7CTSKCYP2D6
SCHEMBL24069882 0.85 CA1 (0.57) CA1CA2CA7CTSKCYP2D6
SCHEMBL22979292 0.85 KMT2A (0.49) CA1CA2CA7CTSKCYP2D6
SCHEMBL18086766 0.85 KMT2A (0.49) CA1CA2CA7CTSKCYP2D6
SCHEMBL305895 0.83 CA1 (0.55) CA1CA2CA7CTSKCYP2D6
SCHEMBL2550753 0.83 CA1 (0.55) CA1CA2CA7CTSKCYP2D6
SCHEMBL7148686 0.83 CA1 (0.55) CA1CA2CA7CTSKCYP2D6
SCHEMBL21676408 0.82 CTSK (0.62) CA1CA2CA7CTSKCYP2D6
SCHEMBL1303375 0.81 CA1 (0.53) CA1CA2CA7CTSKCYP2D6

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2903979-B1 NOVEL COMPOUNDS, THEIR PREPARATION AND THEIR USES INHIBIKASE THERAPEUTICS INC (US) 2020-08-19 EP claimed
CN-102584937-A Crystal forms of (3r)-1-(2-methylalanyl-d-tryptophyl)-3-(phenylmethyl)-3-piperidinecarboxylic acid 1,2,2-trimethylhydrazide HELSINN THERAPEUTICS US INC 2012-07-18 CN claimed
US-20090227618-A2 Carboline Derivatives Useful in the Inhibition of Angiogenesis PTC THERAPEUTICS, INC. (US) 2009-09-10 US claimed
US-20070281962-A2 Administering 1,2,3,6-tetrasubstituted pyrido[3,4-b]indoles to inhibit the 5'-untranslated region-dependent translation; anticarcinogenic agents; retinopathy, rheumatoid arthritis, psoriasis, atherosclerosis, obesity, macular degeneration PCT THERAPEUTICS, INC. (US) 2007-12-06 US claimed
WO-2005089764-A9 CARBOLINE DERIVATIVES USEFUL IN THE INHIBITION OF ANGIOGENESIS PTC THERAPEUTICS INC (US) 2007-09-13 WO claimed
EP-1737461-A1 CARBOLINE DERIVATIVES USEFUL IN THE INHIBITION OF ANGIOGENESIS PTC Therapeutics, Inc. (US) 2007-01-03 EP claimed
US-20050272759-A1 Carboline derivatives useful in the inhibition of angiogenesis PTC THERAPEUTICS, INC. 2005-12-08 US claimed
US-6967216-B2 Amino substituted dibenzothiophene derivatives for the treatment of disorders mediated by NP Y5 receptor ASTRAZENECA AB (SE) 2005-11-22 US claimed
WO-2005089764-A1 CARBOLINE DERIVATIVES USEFUL IN THE INHIBITION OF ANGIOGENESIS PTC THERAPEUTICS, INC. (US) 2005-09-29 WO claimed
EP-1140895-B1 THIOPYRAN COMPOUNDS AS INHIBITORS OF MMP FUJISAWA PHARMACEUTICAL CO (JP) 2004-03-24 EP claimed
US-20030225097-A1 Amino substituted dibenzothiophene derivatives for the treatment of disorders mediated by np y5 receptor ASTRAZENECA AB (SE) 2003-12-04 US claimed
EP-1278739-A1 AMINO SUBSTITUTED DIBENZOTHIOPHENE DERIVATIVES FOR THE TREATMENT OF DISORDERS MEDIATED BY THE NP Y5 RECEPTOR AstraZeneca AB (SE) 2003-01-29 EP claimed
US-6376548-B1 FUNGICIDES; HERBICIDES; INSECTICIDES ROHM AND HAAS COMPANY 2002-04-23 US claimed
WO-2001085714-A1 AMINO SUBSTITUTED DIBENZOTHIOPHENE DERIVATIVES FOR THE TREATMENT OF DISORDERS MEDIATED BY THE NP Y5 RECEPTOR ASTRAZENECA AB (SE) 2001-11-15 WO claimed
EP-1140895-A2 THIOPYRAN COMPOUNDS AS INHIBITORS OF MMP FUJISAWA PHARMACEUTICAL CO., LTD. (JP) 2001-10-10 EP claimed
WO-2000040576-A2 THIOPYRAN COMPOUNDS AS INHIBITORS OF MMP FUJISAWA PHARMACEUTICAL CO., LTD. (JP) 2000-07-13 WO claimed
CN-119302960-A Unit dose compositions of AKT inhibitors 南京正大天晴制药有限公司 2025-01-14 CN disclosed
CN-115916350-B Unit dose compositions of AKT inhibitors 南京正大天晴制药有限公司 2024-11-05 CN disclosed
US-5861429-A MITICIDES AND ANTHELMINTICS SANKYO COMPANY, LIMITED (JP) 1999-01-19 US disclosed
WO-1998040421-A1 CATIONIC GROUP 13 COMPLEXES INCORPORATING BIDENTATE LIGANDS AS POLYMERIZATION CATALYSTS UNIVERSITY OF IOWA RESEARCH FOUNDATION (US) 1998-09-17 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 (4 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-20090227618-A2 Carboline Derivatives Useful in the Inhibition of Angiogenesis VEGFA, FLT4, KDR CA1 3943/4885CA2 875/4885CA7 876/4885
US-20030225097-A1 Amino substituted dibenzothiophene derivatives for the treatment of disorders mediated by np y5 receptor NPY5R, NPY1R, NPY2R CA1 2586/4885CA2 2486/4885CA7 3611/4885
US-20050272759-A1 Carboline derivatives useful in the inhibition of angiogenesis VEGFA, FLT4, KDR CA1 3943/4885CA2 875/4885CA7 876/4885
US-20070281962-A2 Administering 1,2,3,6-tetrasubstituted pyrido[3,4-b]indoles to inhibit the 5'-untranslated region-dependent translation; anticarcinogenic agents; retinopathy, rheumatoid arthritis, psoriasis, atherosclerosis, obesity, macular degeneration VEGFA, FLT4, MIF CA1 4844/4885CA2 4487/4885CA7 4692/4885

“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.