SCHEMBL1265766

SCHEMBL1265766

NC1CCSc2ccccc21

nearest known ligand 0.53

Predicted protein targets (top 7)

geneUniProtsupporting neighboursconfidence
USP2 O75604 1/20 0.45
NPC1 O15118 2/20 0.42
ALPL P05186 1/20 0.41
ALPI P09923 1/20 0.41
MEN1 O00255 2/20 0.40
KMT2A Q03164 2/20 0.40
POLB P06746 1/20 0.38

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
SCHEMBL5387901 1.00 USP2 (0.45) USP2NPC1ALPLALPIMEN1
SCHEMBL5255020 1.00 USP2 (0.45) USP2NPC1ALPLALPIMEN1
Hydrochloric Acid SCHEMBL1003531 0.98 USP2 (0.44) USP2NPC1ALPLALPIMEN1
SCHEMBL1913754 0.88 HCRTR1 (0.44) USP2NPC1ALPLALPIMEN1
SCHEMBL8144693 0.78 HTR2A (0.41) USP2NPC1MEN1KMT2APOLB
SCHEMBL24075123 0.75 USP2 (0.45) USP2NPC1ALPLALPIMEN1
SCHEMBL10373039 0.75 USP2 (0.45) USP2NPC1ALPLALPIMEN1
SCHEMBL12657420 0.75 NPC1 (0.45) USP2NPC1ALPLALPIMEN1
SCHEMBL7556064 0.75 USP2 (0.45) USP2NPC1ALPLALPIMEN1
SCHEMBL12651544 0.75 USP2 (0.45) USP2NPC1ALPLALPIMEN1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-10556878-B2 Thiourea compounds and their use as inhibitors of Sirt2 or Sirt5 CORNELL UNIVERSITY (US) 2020-02-11 US disclosed
US-20160130246-A1 THIOUREA COMPOUNDS AND THEIR USE AS INHIBITORS OF SIRT2 OR SIRT5 NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT 2016-05-12 US disclosed
WO-2014197775-A1 THIOUREA COMPOUNDS AND THEIR USE AS INHIBITORS OF SIRT2 OR SIRT5 CORNELL UNIVERSITY (US) 2014-12-11 WO disclosed
US-7884109-B2 immunosuppressants such as 2-(6-Fluoro-1H-benzo[d]imidazol-1-yl)-9-((1R,4R)-4-hydroxy-1,2,3,4-tetrahydronaphthalen-1-yl)-7H-purin-8(9H)-one, used for the prevention and treatment of autoimmune diseases, inflammatory disease, mast cell mediated disease and transplant rejection WYETH LLC (US) 2011-02-08 US disclosed
US-7884109-B2 immunosuppressants such as 2-(6-Fluoro-1H-benzo[d]imidazol-1-yl)-9-((1R,4R)-4-hydroxy-1,2,3,4-tetrahydronaphthalen-1-yl)-7H-purin-8(9H)-one, used for the prevention and treatment of autoimmune diseases, inflammatory disease, mast cell mediated disease and transplant rejection WYETH LLC (US) 2011-02-08 US disclosed
US-7884109-B2 immunosuppressants such as 2-(6-Fluoro-1H-benzo[d]imidazol-1-yl)-9-((1R,4R)-4-hydroxy-1,2,3,4-tetrahydronaphthalen-1-yl)-7H-purin-8(9H)-one, used for the prevention and treatment of autoimmune diseases, inflammatory disease, mast cell mediated disease and transplant rejection WYETH LLC (US) 2011-02-08 US disclosed
US-20100168102-A9 Amide Derivatives as Kinase Inhibitors DEVGEN NV (BE) 2010-07-01 US disclosed
US-20100168102-A9 Amide Derivatives as Kinase Inhibitors DEVGEN NV (BE) 2010-07-01 US disclosed
US-20100168102-A9 Amide Derivatives as Kinase Inhibitors DEVGEN NV (BE) 2010-07-01 US disclosed
US-20090118283-A1 Amide Derivatives as Kinase Inhibitors DEVGEN NV (BE) 2009-05-07 US disclosed
EP-1134213-A2 Process for the preparation of substituted N-(indole-2-carbonyl)- glycinamides PFIZER INC. (US) 2001-09-19 EP disclosed
US-6277877-B1 GLYCOGEN PHOSPHORYLASE INHIBITOR; ANTIDIABETIC AGENTS PFIZER, INC. 2001-08-21 US disclosed
WO-2000078744-A1 THIOCHROMAN DERIVATIVES AGAINST NEUROLOGICAL DISORDERS ASTRAZENECA UK LIMITED (GB) 2000-12-28 WO disclosed
US-6107329-A HYPOTENSIVE AGENTS; CARDIOVASCULAR DISORDERS PFIZER, INC. (US) 2000-08-22 US disclosed
EP-0832065-A1 SUBSTITUTED N-(INDOLE-2-CARBONYL)-GLYCINAMIDES AND DERIVATIVES AS GLYCOGEN PHOSPHORYLASE INHIBITORS PFIZER INC. (US) 1998-04-01 EP disclosed
WO-1996039384-A1 SUBSTITUTED N-(INDOLE-2-CARBONYL)-GLYCINAMIDES AND DERIVATIVES AS GLYCOGEN PHOSPHORYLASE INHIBITORS PFIZER, INC. (US) 1996-12-12 WO disclosed
EP-0480714-A2 HIV protease inhibitors having symmetrical structure MERCK & CO. INC. (US) 1992-04-15 EP disclosed
US-5035739-A PLANT GROWTH REGULATORS IDEMITSU KOSAN COMPANY LIMITED (JP) 1991-07-30 US disclosed
US-4919705-A PLANT GROWTH REGULATORS IDEMITSU KOSAN COMPANY LIMITED (JP) 1990-04-24 US disclosed
EP-0305529-A1 TRIFLUOROMETHANESULFONAMIDE DERIVATIVES, PROCESS FOR THEIR PREPARATION, AND HERBICIDES CONTAINING SAME IDEMITSU KOSAN COMPANY LIMITED (JP) 1989-03-08 EP 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-20160130246-A1 THIOUREA COMPOUNDS AND THEIR USE AS INHIBITORS OF SIRT2 OR SIRT5 SIRT2, SIRT3, SIRT1 USP2 1003/4885NPC1 2620/4885ALPL 4854/4885
US-20100168102-A9 Amide Derivatives as Kinase Inhibitors MAP3K1, CDK1, CDK2 USP2 2880/4885NPC1 1738/4885ALPL 4417/4885
US-20090118283-A1 Amide Derivatives as Kinase Inhibitors MAP3K1, CDK1, CDK2 USP2 2880/4885NPC1 1738/4885ALPL 4417/4885
US-10556878-B2 Thiourea compounds and their use as inhibitors of Sirt2 or Sirt5 SIRT2, SIRT3, SIRT1 USP2 1003/4885NPC1 2620/4885ALPL 4854/4885

“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.