SCHEMBL1387640

SCHEMBL1387640

[c]1nc(-c2cccnc2)cs1

nearest known ligand 0.50

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CYP19A1 P11511 7/20 0.50
CYP2A6 P11509 7/20 0.50
CYP3A4 P08684 5/20 0.50
ALDH1A1 P00352 4/20 0.50
CYP1A2 P05177 2/20 0.50
AXL P30530 1/20 0.50
PBRM1 Q86U86 1/20 0.50
MKNK1 Q9BUB5 1/20 0.50
MKNK2 Q9HBH9 1/20 0.50
RAB9A P51151 2/20 0.47
NPC1 O15118 1/20 0.47
CYP2C9 P11712 2/20 0.46
CYP2B6 P20813 2/20 0.46
CYP2C19 P33261 1/20 0.46
METAP2 P50579 1/20 0.44
SIRT3 Q9NTG7 1/20 0.44
DYRK1A Q13627 1/20 0.44
DYRK1B Q9Y463 1/20 0.44
KDM4E B2RXH2 2/20 0.44
LMNA P02545 1/20 0.44

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
SCHEMBL443517 0.78 LMNA (0.43) CYP19A1CYP3A4CYP1A2RAB9ANPC1
SCHEMBL7240451 0.76 ATM (0.33) CYP2A6
SCHEMBL5540279 0.75 RAB9A (0.47) CYP2A6CYP3A4ALDH1A1RAB9ANPC1
SCHEMBL17625930 0.74 ATM (0.42) CYP2A6
SCHEMBL29419014 0.70 CYP2A6 (1.00) CYP19A1CYP2A6CYP3A4ALDH1A1CYP1A2
SCHEMBL120088 0.70 CYP2A6 (1.00) CYP19A1CYP2A6CYP3A4ALDH1A1CYP1A2
SCHEMBL30473120 0.70 CYP2A6 (1.00) CYP19A1CYP2A6CYP3A4ALDH1A1CYP1A2
SCHEMBL1830802 0.69 CYP1A2 (0.36) CYP19A1ALDH1A1CYP1A2CYP2C9CYP2C19
SCHEMBL17626098 0.69 KMO (0.51) ALDH1A1RAB9ANPC1KDM4EHPGD
SCHEMBL468087 0.69 CYP19A1 (0.45) CYP19A1RAB9ANPC1MAPTSMN1; 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 89 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-110997663-A Benzofuran ureas or carbamates and heteroaromatic analogs thereof for use in therapy 欧洲分子生物学实验室 2020-04-10 CN claimed
EP-1441719-B1 N-SUBSTITUTED PYRROLIDIN DERIVATIVES AS DIPEPTIDYL PEPTIDASE IV INHIBITORS HOFFMANN LA ROCHE (CH) 2011-03-30 EP claimed
US-7803819-B2 DPP IV inhibitors HOFFMANN-LA ROCHE INC. (US) 2010-09-28 US claimed
CN-1713907-B N-substituted pyrrolidine derivatives as dipeptidyl peptidase IV inhibitors HOFFMANN LA ROCHE 2010-05-26 CN claimed
US-7470701-B2 Substituted 2,5-heterocyclic derivatives NOVARTIS VACCINES AND DIAGNOSTICS, INC. (US) 2008-12-30 US claimed
US-20080255120-A1 SUBSTITUTED 2,5-HETEROCYCLIC DERIVATIVES NOVARTIS VACCINES AND DIAGNOSTICS, INC. (US) 2008-10-16 US claimed
US-20070259925-A1 DPP IV INHIBITORS BOEHRINGER MARKUS 2007-11-08 US claimed
CN-1989131-A Substituted thiophene derivatives as anti-cancer agents CHIRON CORP (US) 2007-06-27 CN claimed
EP-1732919-A1 SUBSTITUTED THIOPHENE DERIVATIVES AS ANTI-CANCER AGENTS CHIRON CORPORATION (US) 2006-12-20 EP claimed
CN-1829721-A Spiro '1-azabicyclo' 2.2.2! octan-3,5'-oxazolidin - 2'-one! derivatives with affinity to the alpha7 nicotinic acetylcholine receptor ASTRAZENECA AB (SE) 2006-09-06 CN claimed
US-20050096348-A1 DPP IV inhibitors BOEHRINGER MARKUS (CH) 2005-05-05 US claimed
EP-1441719-A1 N-SUBSTITUTED PYRROLIDIN DERIVATIVES AS DIPEPTIDYL PEPTIDASE IV INHIBITORS F. HOFFMANN-LA ROCHE AG (CH) 2004-08-04 EP claimed
US-20040116418-A1 Compounds and methods for inhibition of HIV and related viruses MEDIVIR AB (SE) 2004-06-17 US claimed
US-20030130281-A1 DPP IV inhibitors HOFFMAN-LA ROCHE INC. 2003-07-10 US claimed
WO-2003037327-A1 N-SUBSTITUTED PYRROLIDIN DERIVATIVES AS DIPEPTIDYL PEPTIDASE IV INHIBITORS F. HOFFMANN-LA-ROCHE AG (CH) 2003-05-08 WO claimed
US-20020132794-A1 Compounds and methods for inhibition of HIV and related viruses MEDIVIR AB 2002-09-19 US claimed
EP-0706514-B1 COMPOUNDS AND METHODS FOR INHIBITION OF HIV AND RELATED VIRUSES MEDIVIR AB (SE) 1998-11-18 EP claimed
JP-H09502702-A 1997-03-18 JP claimed
EP-0706514-A1 COMPOUNDS AND METHODS FOR INHIBITION OF HIV AND RELATED VIRUSES MEDIVIR AB (SE) 1996-04-17 EP claimed
WO-1995006034-A1 COMPOUNDS AND METHODS FOR INHIBITION OF HIV AND RELATED VIRUSES MEDIVIR AB (SE) 1995-03-02 WO claimed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (5 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-20080255120-A1 SUBSTITUTED 2,5-HETEROCYCLIC DERIVATIVES CYP3A5, ABCG2, ABCB1 CYP19A1 128/4885CYP2A6 44/4885CYP3A4 14/4885
US-20070259925-A1 DPP IV INHIBITORS DPP4, DPP3, DPP7 CYP19A1 887/4885CYP2A6 382/4885CYP3A4 82/4885
US-20020132794-A1 Compounds and methods for inhibition of HIV and related viruses POLRMT, POLM, POLR1E CYP19A1 2848/4885CYP2A6 2465/4885CYP3A4 916/4885
US-20030130281-A1 DPP IV inhibitors DPP4, DPP3, DPP7 CYP19A1 1019/4885CYP2A6 724/4885CYP3A4 171/4885
US-20050096348-A1 DPP IV inhibitors DPP4, DPP3, DPP7 CYP19A1 887/4885CYP2A6 382/4885CYP3A4 82/4885

“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.