SCHEMBL5595239

SCHEMBL5595239

CCCc1c2nc(-c3cc(S(=O)(=O)N4CCN(C)CC4)ccc3OCC)[nH]c(=O)c2nn1Cc1ccccc1

nearest known ligand 0.68

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
PDE5A O76074 20/20 0.68
PDE1A P54750 3/20 0.68
PDE1B Q01064 3/20 0.68
PDE1C Q14123 3/20 0.68
ABCC4 O15439 2/20 0.68
PDE4B Q07343 2/20 0.68
PDE2A O00408 1/20 0.68
ABCC5 O15440 1/20 0.68
PDE6D O43924 1/20 0.68
PDE8A O60658 1/20 0.68
PDE9A O76083 1/20 0.68
ABCB11 O95342 1/20 0.68
CYP3A4 P08684 1/20 0.68
HTR1A P08908 1/20 0.68
PDE6A P16499 1/20 0.68
PDE6G P18545 1/20 0.68
PDE4A P27815 1/20 0.68
ADORA2A P29274 1/20 0.68
ADORA1 P30542 1/20 0.68
ADRA1A P35348 1/20 0.68

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
SCHEMBL6334389 0.93 PDE5A (0.66) PDE5APDE1APDE1BPDE1CABCC4
SCHEMBL6334615 0.93 PDE5A (0.66) PDE5APDE1APDE1BPDE1CABCC4
SCHEMBL6333008 0.91 PDE5A (0.65) PDE5APDE1APDE1BPDE1CABCC4
SCHEMBL6332513 0.91 PDE5A (0.72) PDE5APDE1APDE1BPDE1CABCC4
SCHEMBL6338193 0.90 PDE5A (0.63) PDE5APDE1APDE1BPDE1CABCC4
SCHEMBL14836455 0.88 PDE5A (0.75) PDE5APDE1APDE1BPDE1CABCC4
SCHEMBL5595162 0.88 PDE5A (0.78) PDE5APDE1APDE1BPDE1CABCC4
SCHEMBL6338376 0.87 PDE5A (0.63) PDE5APDE1APDE1BPDE1CABCC4
SCHEMBL5595563 0.86 PDE5A (0.67) PDE5APDE1APDE1BPDE1CABCC4
SCHEMBL6332267 0.86 PDE5A (0.62) PDE5APDE1APDE1BPDE1CABCC4

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 6 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20070197560-A1 cGMP PDE 5 inhibitors for inhalation in the treatment of sexual dysfunction NAEF RETO 2007-08-23 US disclosed
US-6916927-B2 Pyrazolopyrimidinones which inhibit type 5 cyclic guanosine 3′,5′-monophosphate phosphodiesterase (cGMP-PDE5) for the treatment of sexual dysfunction PFIZER INC. 2005-07-12 US disclosed
US-20040214831-A1 cGMP PDE 5 inhibitors for inhalation in the treatment of sexual dysfunction NAEF RETO 2004-10-28 US disclosed
US-20040180944-A1 Pyrazolopyrimidinones which inhibit type 5 cyclic guanosine 3',5'-monophosphate phosphodiesterase (cGMP-PDE5) for the treatment of sexual dysfunction PFIZER INC 2004-09-16 US disclosed
US-6723719-B1 DYSMENORRHOEA, BENIGN PROSTATIC HYPERPLASIA (BPH), BLADDER OUTLET OBSTRUCTION, INCONTINENCE, AGINA, CONGESTIVE HEART FAILURE, ATHEROSCLEROSIS; HYPOTENSIVE AND ANTIALLERGEN AGENTS PFIZER INC 2004-04-20 US disclosed
US-20010055570-A1 Cyclic guanosine 3',5'-monophosphate phosphodiesterases (cGMP PDEs); using specified pyrazolopyrimidinone or aminoquinazoline derivatives NAEF RETO (CH) 2001-12-27 US 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 (1 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-20040180944-A1 Pyrazolopyrimidinones which inhibit type 5 cyclic guanosine 3',5'-monophosphate phosphodiesterase (cGMP-PDE5) for the treatment of sexual dysfunction PDE5A, PDE3A, PDE3B PDE5A 1/4885PDE1A 38/4885PDE1B 49/4885

“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.