SCHEMBL6442718

SCHEMBL6442718

CCN1CCN(S(=O)(=O)c2cnc(OC3CCN(C)CC3)c(C(=O)O)c2)CC1.[NaH]

nearest known ligand 0.70

Predicted protein targets (top 19)

geneUniProtsupporting neighboursconfidence
KMT2A Q03164 2/20 0.70
PDE5A O76074 6/20 0.46
ALDH1A1 P00352 3/20 0.45
CYP2D6 P10635 1/20 0.43
POLB P06746 1/20 0.39
PKM P14618 1/20 0.39
GAA P10253 2/20 0.39
KDM4E B2RXH2 1/20 0.39
LMNA P02545 1/20 0.38
NPC1 O15118 1/20 0.38
RAB9A P51151 1/20 0.38
APOBEC3A P31941 1/20 0.38
APOBEC3G Q9HC16 1/20 0.38
MAPT P10636 1/20 0.38
HPGD P15428 1/20 0.38
CYP2C19 P33261 1/20 0.38
HSD17B10 Q99714 1/20 0.38
PIK3CD O00329 1/20 0.38
PIK3CA P42336 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
SCHEMBL6442726 0.99 KMT2A (0.71) KMT2APDE5AALDH1A1CYP2D6POLB
SCHEMBL6444485 0.90 KMT2A (0.68) KMT2APDE5AALDH1A1CYP2D6PKM
SCHEMBL6442720 0.90 KMT2A (0.57) KMT2APDE5AALDH1A1CYP2D6PKM
SCHEMBL6444270 0.89 KMT2A (0.59) KMT2APDE5AALDH1A1CYP2D6POLB
SCHEMBL6446723 0.84 ALDH1A1 (0.59) KMT2APDE5AALDH1A1CYP2D6GAA
SCHEMBL6441696 0.84 KMT2A (0.98) KMT2APDE5AALDH1A1CYP2D6PKM
SCHEMBL3587341 0.82 KMT2A (1.00) KMT2APDE5AALDH1A1CYP2D6PKM
SCHEMBL6200528 0.82 KMT2A (0.83) KMT2APDE5AALDH1A1CYP2D6PKM
SCHEMBL6441707 0.82 KMT2A (1.00) KMT2APDE5AALDH1A1CYP2D6PKM
Hydrochloric Acid SCHEMBL6386723 0.81 KMT2A (0.98) KMT2APDE5AALDH1A1CYP2D6PKM

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
EP-1371647-B1 Pyridine-3-carboxylic acid derivatives and their use as intermediates PFIZER (US) 2005-07-13 EP disclosed
EP-1371647-A2 Pyridine-3-carboxylic acid derivatives and their use as intermediates PFIZER INC. (US) 2003-12-17 EP disclosed
EP-1073658-B1 PYRAZOLOPYRIMIDINONE CGMP PDE5 INHIBITORS FOR THE TREATMENT OF SEXUAL DYSFUNCTION PFIZER (US) 2003-08-13 EP disclosed
US-6458951-B2 FOR TREATMENT OF MALE ERECTILE DYSFUNCTION, FEMALE SEXUAL DYSFUNCTION PFIZER INC 2002-10-01 US disclosed
US-20010039271-A1 Pyrazolopyrimidinone cGMP PDE5 inhibitors for the treatment of sexual dysfunction BUNNAGE MARK EDWARD (GB) 2001-11-08 US disclosed
US-6251904-B1 Pyrazolopyrimidinone cGMP PDE5 inhibitors for the treatment of sexual dysfunction PFIZER INC. 2001-06-26 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-20010039271-A1 Pyrazolopyrimidinone cGMP PDE5 inhibitors for the treatment of sexual dysfunction PDE5A, PDE3A, PDE3B KMT2A 4533/4885PDE5A 1/4885ALDH1A1 254/4885

“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.