SCHEMBL5307

SCHEMBL5307

CCCc1nc(C)c2c(=O)[nH]c(-c3cc(S(=O)(=O)Cl)ccc3OCC)nn12

nearest known ligand 0.75

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
PDE5A O76074 18/20 0.75
PDE1A P54750 8/20 0.75
PDE1B Q01064 8/20 0.75
PDE1C Q14123 8/20 0.75
PDE4B Q07343 2/20 0.75
PDE6A P16499 2/20 0.73
PDE2A O00408 1/20 0.73
PDE6D O43924 1/20 0.73
PDE9A O76083 1/20 0.73
CHRM2 P08172 1/20 0.73
ADORA3 P0DMS8 1/20 0.73
PDE6G P18545 1/20 0.73
MAOA P21397 1/20 0.73
PDE4A P27815 1/20 0.73
ADORA1 P30542 1/20 0.73
ADRA1A P35348 1/20 0.73
PDE6B P35913 1/20 0.73
PDE6C P51160 1/20 0.73
SLC6A3 Q01959 1/20 0.73
PDE4C Q08493 1/20 0.73

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
SCHEMBL29655362 1.00 PDE5A (0.75) PDE5APDE1APDE1BPDE1CPDE4B
SCHEMBL6340102 0.94 PDE5A (0.67) PDE5APDE1APDE1BPDE1CPDE4B
SCHEMBL974554 0.94 PDE5A (0.66) PDE5APDE1APDE1BPDE1CPDE4B
SCHEMBL6330112 0.93 PDE5A (0.66) PDE5APDE1APDE1BPDE1CPDE4B
SCHEMBL6332643 0.93 PDE5A (0.66) PDE5APDE1APDE1BPDE1CPDE4B
SCHEMBL6334314 0.93 PDE5A (0.66) PDE5APDE1APDE1BPDE1CPDE4B
SCHEMBL8220166 0.92 PDE5A (0.76) PDE5APDE1APDE1BPDE1CPDE4B
SCHEMBL5931959 0.91 PDE5A (0.75) PDE5APDE1APDE1BPDE1CPDE4B
SCHEMBL30594464 0.91 PDE5A (0.75) PDE5APDE1APDE1BPDE1CPDE4B
SCHEMBL29663760 0.91 PDE5A (0.77) PDE5APDE1APDE1BPDE1CPDE4B

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-9845328-B2 Method for manufacturing of vardenafil and its salts ZAKLADY FARMACEUTYCZNE POLPHARMA S.A. (PL) 2017-12-19 US claimed
WO-2023244059-A1 METHODS OF TREATING CANCER USING DUAL ANDROGEN RECEPTOR AND PDE5 INHIBITOR COMPOUNDS ILDONG PHARMACEUTICAL CO., LTD. (KR) 2023-12-21 WO disclosed
EP-4259634-A1 NOVEL COMPOUNDS AS ANDROGEN RECEPTOR AND PHOSPHODIESTERASE DUAL INHIBITOR Ildong Pharmaceutical Co., Ltd. (KR) 2023-10-18 EP disclosed
US-11787812-B2 Substituted pyrazolo[4,3-d]pyrimidines and imidazo[5,1 -f][1,2,4]triazines as androgen receptor and phosphodiesterase dual inhibitors ILDONG PHARMACEUTICAL CO., LTD. (KR) 2023-10-17 US disclosed
US-11787812-B2 Substituted pyrazolo[4,3-d]pyrimidines and imidazo[5,1 -f][1,2,4]triazines as androgen receptor and phosphodiesterase dual inhibitors ILDONG PHARMACEUTICAL CO., LTD. (KR) 2023-10-17 US disclosed
US-11787812-B2 Substituted pyrazolo[4,3-d]pyrimidines and imidazo[5,1 -f][1,2,4]triazines as androgen receptor and phosphodiesterase dual inhibitors ILDONG PHARMACEUTICAL CO., LTD. (KR) 2023-10-17 US disclosed
CN-116848116-A Novel compounds as dual androgen receptor and phosphodiesterase inhibitors 日东制药株式会社 2023-10-03 CN disclosed
US-20220380376-A1 Nitrogen Oxide-Donating PDE-5 and/or PDE-6 Inhibitor Compounds ILDONG PHARMACEUTICAL CO., LTD. (KR) 2022-12-01 US disclosed
EP-4058457-A2 NITROGEN OXIDE-DONATING PDE-5 AND/OR PDE-6 INHIBITOR COMPOUNDS Ildong Pharmaceutical Co., Ltd. (KR) 2022-09-21 EP disclosed
CN-115038704-A Nitrogen oxide donating PDE-5 and/or PDE-6 inhibitor compounds 日东制药股份有限公司 2022-09-09 CN disclosed
US-20050070541-A1 2-Phenyl substituted imidazotriazinones as phosphodiesterase inhibitors BAYER AKTIENGESELLSCHAFT (DE) 2005-03-31 US disclosed
US-20040067945-A1 2-phenyl substituted imidazotriazinones as phosphodiesterase inhibitors BAYER INTELLECTUAL PROPERTY GMBH (DE) 2004-04-08 US disclosed
EP-1368353-A1 2-ALKOXYPHENYL SUBSTITUTED IMIDAZOTRIAZINONES Bayer Aktiengesellschaft (DE) 2003-12-10 EP disclosed
US-6566360-B1 Administering 2-phenyl-substituted imidazotriazinones having short, unbranched alkyl radicals in the 9-position for therapy of hypertrophy of the prostate, incontinence or female sexual dysfunction in mammals BAYER AKTIENGESELLSCHAFT (DE) 2003-05-20 US disclosed
WO-2002064593-A1 2-ALKOXYPHENYL SUBSTITUTED IMIDAZOTRIAZINONES BAYER AKTIENGESELLSCHAFT (DE) 2002-08-22 WO disclosed
US-6362178-B1 TREATMENT OF CARDIOVASCULAR DIORDERS, CEREBROVASCULAR DISORDERS, UROGENITAL DISORDERS AND ERECTILE DYSFUNCTION BAYER AKTIENGESELLSCHAFT (DE) 2002-03-26 US disclosed
EP-1049695-B1 2-PHENYL SUBSTITUTED IMIDAZOTRIAZINONES AS PHOSPHODIESTERASE INHIBITORS BAYER AG (DE) 2002-02-13 EP disclosed
EP-1174431-A2 2-Phenyl-substituited Imidazotriazinones as Phoshodiesterase Inhibitors Bayer Aktiengesellschaft (DE) 2002-01-23 EP disclosed
EP-1049695-A1 2-PHENYL SUBSTITUTED IMIDAZOTRIAZINONES AS PHOSPHODIESTERASE INHIBITORS BAYER AG (DE) 2000-11-08 EP disclosed
WO-1999024433-A1 2-PHENYL SUBSTITUTED IMIDAZOTRIAZINONES AS PHOSPHODIESTERASE INHIBITORS BAYER AKTIENGESELLSCHAFT (DE) 1999-05-20 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-20220380376-A1 Nitrogen Oxide-Donating PDE-5 and/or PDE-6 Inhibitor Compounds PDE6G, PRKG1, PRKG2 PDE5A 4/4885PDE1A 27/4885PDE1B 28/4885
US-20050070541-A1 2-Phenyl substituted imidazotriazinones as phosphodiesterase inhibitors PDE3B, PDE3A, PDE2A PDE5A 4/4885PDE1A 25/4885PDE1B 14/4885
US-11787812-B2 Substituted pyrazolo[4,3-d]pyrimidines and imidazo[5,1 -f][1,2,4]triazines as androgen receptor and phosphodiesterase dual inhibitors PDE5A, AR, PDE3A PDE5A 1/4885PDE1A 7/4885PDE1B 9/4885
US-20040067945-A1 2-phenyl substituted imidazotriazinones as phosphodiesterase inhibitors PDE3B, PDE3A, PDE2A PDE5A 4/4885PDE1A 25/4885PDE1B 14/4885

“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.