SCHEMBL2086656

SCHEMBL2086656

CC1(c2ccccc2)NC(=N)c2ccccc21

nearest known ligand 0.40

Predicted protein targets (top 18)

geneUniProtsupporting neighboursconfidence
▸ ALDH1A1 P00352 3/20 0.40
▸ CFTR P13569 1/20 0.35
▸ GOPC Q9HD26 1/20 0.35
▸ LMNA P02545 1/20 0.35
▸ HTR5A P47898 2/20 0.34
▸ CYP19A1 P11511 2/20 0.33
▸ PDK2 Q15119 1/20 0.33
▸ PDK4 Q16654 1/20 0.33
▸ NOS2 P35228 1/20 0.33
▸ MMP2 P08253 1/20 0.33
▸ MMP9 P14780 1/20 0.33
▸ GAA P10253 1/20 0.32
▸ SMN1; SMN2 Q16637 1/20 0.32
▸ ATM Q13315 1/20 0.32
▸ CYP3A4 P08684 1/20 0.32
▸ HSD17B10 Q99714 1/20 0.32
▸ TDP1 Q9NUW8 1/20 0.32
▸ ITGA4 P13612 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
SCHEMBL8240792 0.85 BACE1 (0.36) ALDH1A1PDK2TDP1
SCHEMBL8238535 0.83 NPSR1 (0.38) ALDH1A1PDK2
SCHEMBL28555391 0.79 NOS2 (0.43) ALDH1A1LMNAHTR5ACYP19A1PDK2
SCHEMBL29976483 0.79 NOS2 (0.43) ALDH1A1LMNAHTR5ACYP19A1PDK2
SCHEMBL15693096 0.78 PDK2 (0.42) ALDH1A1LMNAPDK2SMN1; SMN2HSD17B10
SCHEMBL27927123 0.78 PDK2 (0.36) ALDH1A1LMNAHTR5APDK2PDK4
SCHEMBL2086654 0.77 PGR (0.44) PDK2
SCHEMBL2084820 0.75 BACE1 (0.49) CYP19A1PDK2
SCHEMBL2085277 0.75 BACE1 (0.46) —
SCHEMBL8248134 0.74 PGR (0.46) PDK2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20110059992-A1 New Compounds ASTRAZENECA AB (SE) 2011-03-10 — — US claimed
CN-101506162-A Substituted isoindoles as bace inhibitors and their use ASTRAZENECA AB (SE) 2009-08-12 — — CN claimed
EP-2035378-A1 SUBSTITUTED ISOINDOLES AS BACE INHIBITORS AND THEIR USE AstraZeneca AB (SE) 2009-03-18 — — EP claimed
US-20080171771-A1 New Compounds 391 ASTRAZENECA AB (SE) 2008-07-17 — — US claimed
WO-2007149033-A1 SUBSTITUTED ISOINDOLES AS BACE INHIBITORS AND THEIR USE ASTRAZENECA AB (SE) 2007-12-27 — — WO claimed
US-9382242-B2 Preparation and use of compounds as protease inhibitors MERCK SHARP & DOHME CORP. (US) 2016-07-05 — — US disclosed
US-9382242-B2 Preparation and use of compounds as protease inhibitors MERCK SHARP & DOHME CORP. (US) 2016-07-05 — — US disclosed
US-20140206715-A1 PREPARATION AND USE OF COMPOUNDS AS PROTEASE INHIBITORS PHARMACOPEIA, LLC 2014-07-24 — — US disclosed
US-20140206715-A1 PREPARATION AND USE OF COMPOUNDS AS PROTEASE INHIBITORS PHARMACOPEIA, LLC 2014-07-24 — — US disclosed
US-8722708-B2 Substituted isoindolines as aspartyl protease inhibitors Merck Sharp & Dohme Inc. (US) 2014-05-13 — — US disclosed
US-8722708-B2 Substituted isoindolines as aspartyl protease inhibitors Merck Sharp & Dohme Inc. (US) 2014-05-13 — — US disclosed
EP-2345411-B1 Heterocyclic aspartyl protease inhibitors, preparation and use thereof MERCK SHARP & DOHME (US) 2013-10-02 — — EP disclosed
US-7855213-B2 Compounds ASTRAZENECA AB (SE) 2010-12-21 — — US disclosed
CN-101506162-A Substituted isoindoles as bace inhibitors and their use ASTRAZENECA AB (SE) 2009-08-12 — — CN disclosed
EP-2035378-A1 SUBSTITUTED ISOINDOLES AS BACE INHIBITORS AND THEIR USE AstraZeneca AB (SE) 2009-03-18 — — EP disclosed
US-20080176868-A1 pyrrole/pyrimidine-2-imine fused ring derivatives; aspartyl proteases, beta-secretase inhibitor; cardiovascular diseases, cognitive and neurodegenerative diseases such as Alzheimer's, Human Immunodeficiency Virus, plasmepins, cathepsin D and protozoal enzymes SCHERING CORPORATION 2008-07-24 — — US disclosed
US-20080176868-A1 pyrrole/pyrimidine-2-imine fused ring derivatives; aspartyl proteases, beta-secretase inhibitor; cardiovascular diseases, cognitive and neurodegenerative diseases such as Alzheimer's, Human Immunodeficiency Virus, plasmepins, cathepsin D and protozoal enzymes SCHERING CORPORATION 2008-07-24 — — US disclosed
US-20080171771-A1 New Compounds 391 ASTRAZENECA AB (SE) 2008-07-17 — — US disclosed
WO-2007149033-A1 SUBSTITUTED ISOINDOLES AS BACE INHIBITORS AND THEIR USE ASTRAZENECA AB (SE) 2007-12-27 — — WO disclosed
WO-2006138265-A2 HETEROCYCLIC ASPARTYL PROTEASE INHIBITORS, PREPARATION AND USE THEREOF SCHERING CORPORATION (US) 2006-12-28 — — 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-20140206715-A1 PREPARATION AND USE OF COMPOUNDS AS PROTEASE INHIBITORS CTRL, BACE1, PRSS1 ALDH1A1 4342/4885CFTR 3353/4885GOPC 3644/4885
US-20110059992-A1 New Compounds MAPT, PSEN2, PSEN1 ALDH1A1 2499/4885CFTR 3313/4885GOPC 2721/4885
US-20080176868-A1 pyrrole/pyrimidine-2-imine fused ring derivatives; aspartyl proteases, beta-secretase inhibitor; cardiovascular diseases, cognitive and neurodegenerative diseases such as Alzheimer's, Human Immunodeficiency Virus, plasmepins, cathepsin D and protozoal enzymes BACE1, CTSL, CPN1 ALDH1A1 4821/4885CFTR 4791/4885GOPC 2144/4885
US-20080171771-A1 New Compounds 391 PSEN2, PSEN1, MAPT ALDH1A1 2077/4885CFTR 3340/4885GOPC 2455/4885

“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.

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