Vardenafil

Vardenafil

SCHEMBL5441

CCCc1nc(C)c2c(=O)[nH]c(-c3cc(S(=O)(=O)N4CCN(CC)CC4)ccc3OCC)nn12.Cl.O.O.O

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

PDE5A

The experimentally established mechanism targets of Vardenafil. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
PDE5A known ✓ O76074 20/20 1.00
PDE6A P16499 3/20 1.00
PDE1A P54750 8/20 0.97
PDE1B Q01064 8/20 0.97
PDE1C Q14123 8/20 0.97
PDE4B Q07343 3/20 0.97
PDE3B Q13370 3/20 0.97
PDE3A Q14432 3/20 0.97
PDE2A O00408 2/20 0.97
PDE6D O43924 2/20 0.97
PDE9A O76083 2/20 0.97
PDE6G P18545 2/20 0.97
PDE4A P27815 2/20 0.97
ADORA1 P30542 2/20 0.97
ADRA1A P35348 2/20 0.97
PDE6B P35913 2/20 0.97
PDE6C P51160 2/20 0.97
PDE4C Q08493 2/20 0.97
PDE4D Q08499 2/20 0.97
KCNH2 Q12809 2/20 0.97

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
Vardenafil SCHEMBL973820 0.99 PDE5A (1.00) PDE5APDE6APDE1APDE1BPDE1C
Vardenafil SCHEMBL5685 0.99 PDE5A (1.00) PDE5APDE6APDE1APDE1BPDE1C
Vardenafil SCHEMBL5772 0.98 PDE5A (1.00) PDE5APDE6APDE1APDE1BPDE1C
Vardenafil SCHEMBL29390262 0.98 PDE5A (1.00) PDE5APDE6APDE1APDE1BPDE1C
SCHEMBL24418486 0.93 PDE5A (0.90) PDE5APDE6APDE1APDE1BPDE1C
SCHEMBL31347918 0.93 PDE5A (0.90) PDE5APDE6APDE1APDE1BPDE1C
Hydrochloric Acid SCHEMBL974638 0.92 PDE5A (0.98) PDE5APDE6APDE1APDE1BPDE1C
SCHEMBL19197262 0.92 PDE5A (0.88) PDE5APDE6APDE1APDE1BPDE1C
Hydrochloric Acid SCHEMBL973844 0.92 PDE5A (0.98) PDE5APDE6APDE1APDE1BPDE1C
SCHEMBL13694 0.91 PDE5A (0.87) PDE5APDE6APDE1APDE1BPDE1C

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7696206-B2 2-phenyl substituted imidazotriazinones as phosphodiesterase inhibitors BAYER SCHERING PHARMA AKTIENGESELLSCHAFT (DE) 2010-04-13 US claimed
US-20100016323-A1 2-PHENYL SUBSTITUTED IMIDAZOTRIAZINONES AS PHOSPHODIESTERASE INHIBITORS BAYER SCHERING PHARMA AKTIENGESELLSCHAFT (DE) 2010-01-21 US claimed
EP-1392314-B1 NOVEL USE OF 2-[2-Ethoxy-5-(4-methyl-piperazin-1-sulfonyl)-phenyl]-5-methyl-7-propyl-3H-imidazo[5,1-f][1,2,4]triazin-4-on BAYER HEALTHCARE AG (DE) 2006-12-20 EP claimed
US-20060189624-A1 Novel combination for treating sexual dysfunction BAYER AKTIENGESELLSCHAFT (DE) 2006-08-24 US claimed
EP-1216039-B1 NOVEL COMBINATION FOR THE TREATMENT OF SEXUAL DYSFUNCTION BAYER HEALTHCARE AG (DE) 2005-03-16 EP claimed
EP-3083629-B1 THE METHOD FOR MANUFACTURING OF VARDENAFIL AND ITS SALTS ZAKL FARMACEUTYCZNE POLPHARMA SA (PL) 2021-03-31 EP disclosed
US-9845328-B2 Method for manufacturing of vardenafil and its salts ZAKLADY FARMACEUTYCZNE POLPHARMA S.A. (PL) 2017-12-19 US disclosed
US-20160311827-A1 THE METHOD FOR MANUFACTURING OF VARDENAFIL AND ITS SALTS ZAKLADY FARMACEUTYCZNE POLPHARMA S.A. (PL) 2016-10-27 US disclosed
US-20130059844-A1 2-PHENYL SUBSTITUTED IMIDAZOTRIAZINONES AS PHOSPHODIESTERASE INHIBITORS BAYER SCHERING PHARMA AKTIENGESELLSCHAFT (DE) 2013-03-07 US disclosed
EP-2295436-A1 2-Phenyl-subsitituted Imidazotriazinones as Phosphodiesterase V inhibitors Bayer Schering Pharma AG (DE) 2011-03-16 EP disclosed
US-20110009367-A1 2-PHENYL SUBSTITUTED IMIDAZOTRIAZINONES AS PHOSPHODIESTERASE INHIBITORS BAYER SCHERING PHARMA AKTIENGESELLSCHAFT (DE) 2011-01-13 US disclosed
US-7704999-B2 2-phenyl substituted imidazotriazinones as phosphodiesterase inhibitors BAYER SCHERING PHARMA AKTIENGESELLSCHAFT (DE) 2010-04-27 US disclosed
US-20040152700-A1 Novel use of 2-phenyl-substituted imidazotriazinones BAYER SCHERING PHARMA AKTIENGESELLSCHAFT (DE) 2004-08-05 US disclosed
US-20040067945-A1 2-phenyl substituted imidazotriazinones as phosphodiesterase inhibitors BAYER INTELLECTUAL PROPERTY GMBH (DE) 2004-04-08 US 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
EP-1216039-A2 NOVEL COMBINATION FOR THE TREATMENT OF SEXUAL DYSFUNCTION Bayer Aktiengesellschaft (DE) 2002-06-26 EP 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
WO-2001019357-A2 COMBINATION PREPARATION FOR THE TREATMENT OF SEXUAL DYSFUNCTION BAYER AKTIENGESELLSCHAFT (DE) 2001-03-22 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 (7 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-20100016323-A1 2-PHENYL SUBSTITUTED IMIDAZOTRIAZINONES AS PHOSPHODIESTERASE INHIBITORS PDE3A, PDE2A, PDE3B PDE5A 4/4885PDE6A 17/4885PDE1A 18/4885
US-20110009367-A1 2-PHENYL SUBSTITUTED IMIDAZOTRIAZINONES AS PHOSPHODIESTERASE INHIBITORS PDE3B, PDE3A, PDE2A PDE5A 4/4885PDE6A 11/4885PDE1A 25/4885
US-20060189624-A1 Novel combination for treating sexual dysfunction PDE3B, PDE3A, PDE2A PDE5A 4/4885PDE6A 17/4885PDE1A 14/4885
US-20130059844-A1 2-PHENYL SUBSTITUTED IMIDAZOTRIAZINONES AS PHOSPHODIESTERASE INHIBITORS PDE3B, PDE3A, PDE2A PDE5A 4/4885PDE6A 11/4885PDE1A 25/4885
US-20040067945-A1 2-phenyl substituted imidazotriazinones as phosphodiesterase inhibitors PDE3B, PDE3A, PDE2A PDE5A 4/4885PDE6A 11/4885PDE1A 25/4885
US-20160311827-A1 THE METHOD FOR MANUFACTURING OF VARDENAFIL AND ITS SALTS CYP3A5, KDM5A, KDM5C PDE5A 6/4885PDE6A 189/4885PDE1A 565/4885
US-20040152700-A1 Novel use of 2-phenyl-substituted imidazotriazinones PDE7A, PDE4A, PDE5A PDE5A 3/4885PDE6A 20/4885PDE1A 4/4885

“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.