SCHEMBL2634372

SCHEMBL2634372

O=S1(=O)CCN(Cc2cccc(Br)c2)CC1

nearest known ligand 0.68

Predicted protein targets (top 19)

geneUniProtsupporting neighboursconfidence
SMN1; SMN2 Q16637 1/20 0.66
TDP1 Q9NUW8 1/20 0.66
LMNA P02545 1/20 0.62
MBTD1 Q05BQ5 1/20 0.55
L3MBTL3 Q96JM7 1/20 0.55
KMT2A Q03164 4/20 0.53
MEN1 O00255 3/20 0.53
KDM4E B2RXH2 2/20 0.52
FAAH O00519 1/20 0.51
SIGMAR1 Q99720 2/20 0.47
POLB P06746 1/20 0.46
CA12 O43570 1/20 0.46
CA2 P00918 1/20 0.46
CA9 Q16790 1/20 0.46
ALDH1A1 P00352 1/20 0.45
HTT P42858 1/20 0.45
CYP1A2 P05177 1/20 0.45
CYP2C19 P33261 1/20 0.45
DRD4 P21917 2/20 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
SCHEMBL29197757 0.81 SMN1; SMN2 (0.72) SMN1; SMN2TDP1MBTD1L3MBTL3KMT2A
SCHEMBL9025487 0.81 SMN1; SMN2 (0.96) SMN1; SMN2TDP1MBTD1L3MBTL3KMT2A
SCHEMBL13981948 0.81 LMNA (0.67) TDP1LMNAKMT2AMEN1KDM4E
SCHEMBL18946202 0.81 LMNA (0.62) LMNAKMT2AMEN1FAAHSIGMAR1
SCHEMBL18423019 0.81 LMNA (0.62) LMNAKMT2AMEN1FAAHSIGMAR1
SCHEMBL11860 0.81 MEN1 (0.66) LMNAKMT2AMEN1KDM4EFAAH
SCHEMBL1367503 0.80 SMN1; SMN2 (0.70) SMN1; SMN2TDP1LMNAMBTD1L3MBTL3
SCHEMBL3641561 0.80 SMN1; SMN2 (1.00) SMN1; SMN2TDP1MBTD1L3MBTL3KDM4E
SCHEMBL6818314 0.80 SMN1; SMN2 (0.93) SMN1; SMN2TDP1MBTD1L3MBTL3KMT2A
SCHEMBL1427500 0.80 KMT2A (0.69) LMNAKMT2AMEN1KDM4EPOLB

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-8633173-B2 Preparation and uses of 1,2,4-triazolo [1,5a] pyridine derivatives CEPHALON, INC (US) 2014-01-21 US disclosed
US-20130296312-A1 Preparation and Uses of 1,2,4-Triazolo [1,5a] Pyridine Derivatives CEPHALON, INC. 2013-11-07 US disclosed
US-8501936-B2 Preparation and uses of 1,2,4-triazolo [1,5a] pyridine derivatives CEPHALON, INC. (US) 2013-08-06 US disclosed
EP-2438066-A2 PREPARATION AND USES OF 1,2,4-TRIAZOLO [1,5a]PYRIDINE DERIVATIVES Cephalon, Inc. (US) 2012-04-11 EP disclosed
US-20100311693-A1 Preparation and Uses of 1,2,4-Triazolo [1,5a] Pyridine Derivatives CEPHALON, INC. (US) 2010-12-09 US disclosed
WO-2010141796-A2 PREPARATION AND USES OF 1,2,4-TRIAZOLO [1,5a] PYRIDINE DERIVATIVES CEPHALON, INC. (US) 2010-12-09 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 (2 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-20130296312-A1 Preparation and Uses of 1,2,4-Triazolo [1,5a] Pyridine Derivatives JAK2, JAK1, JAK3 SMN1; SMN2 3360/4885TDP1 1611/4885LMNA 2075/4885
US-20100311693-A1 Preparation and Uses of 1,2,4-Triazolo [1,5a] Pyridine Derivatives CCNA1, CCNY, RB1 SMN1; SMN2 3192/4885TDP1 266/4885LMNA 835/4885

“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.