SCHEMBL354653

SCHEMBL354653

CCc1noc(C)c1C(=O)N(C)Cc1csc(NC(=O)NCc2ccc(Cl)c(Cl)c2)n1

nearest known ligand 0.52

Predicted protein targets (top 18)

geneUniProtsupporting neighboursconfidence
LMNA P02545 2/20 0.46
HTT P42858 2/20 0.46
SMN1; SMN2 Q16637 2/20 0.46
GAA P10253 2/20 0.46
MAPT P10636 1/20 0.46
GPR55 Q9Y2T6 1/20 0.46
RAB9A P51151 3/20 0.42
NPC1 O15118 2/20 0.42
P2RX7 Q99572 1/20 0.41
KMT2A Q03164 2/20 0.40
TDP1 Q9NUW8 2/20 0.40
CYP1A2 P05177 1/20 0.40
CYP2C9 P11712 1/20 0.40
CYP2C19 P33261 1/20 0.40
ROCK2 O75116 3/20 0.38
ROCK1 Q13464 3/20 0.38
TSHR P16473 2/20 0.38
HSD17B10 Q99714 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
SCHEMBL353096 0.91 P2RX7 (0.46) LMNAGAARAB9ANPC1P2RX7
SCHEMBL355096 0.88 BACE1 (0.46) LMNASMN1; SMN2GAAMAPTRAB9A
SCHEMBL353398 0.88 P2RX7 (0.40) GAAP2RX7KMT2ATDP1CYP1A2
SCHEMBL353432 0.87 ROCK2 (0.49) LMNAHTTSMN1; SMN2GAAMAPT
SCHEMBL353637 0.84 RAB9A (0.41) SMN1; SMN2MAPTRAB9ANPC1P2RX7
SCHEMBL352139 0.84 ROCK1 (0.44) ROCK2ROCK1
SCHEMBL354526 0.84 ROCK1 (0.42) LMNASMN1; SMN2GAAMAPTKMT2A
SCHEMBL883885 0.83 P2RX7 (0.45) LMNAGAARAB9ANPC1P2RX7
SCHEMBL354560 0.83 P2RX7 (0.47) LMNAHTTSMN1; SMN2GAAMAPT
SCHEMBL352968 0.83 ROCK1 (0.41) LMNASMN1; SMN2GAAMAPTP2RX7

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-2200440-B1 ANTIBACTERIAL AMIDE AND SULFONAMIDE SUBSTITUTED HETEROCYCLIC UREA COMPOUNDS CRESTONE INC (US) 2017-07-19 EP claimed
US-8148380-B2 Antibacterial amide and sulfonamide substituted heterocyclic urea compounds CRESTONE, INC. (US) 2012-04-03 US claimed
US-20120015941-A1 Antibacterial Amide and Sulfonamide Substituted Heterocyclic Urea Compounds CRESTONE, INC. (US) 2012-01-19 US claimed
EP-2200440-B1 ANTIBACTERIAL AMIDE AND SULFONAMIDE SUBSTITUTED HETEROCYCLIC UREA COMPOUNDS CRESTONE INC (US) 2017-07-19 EP disclosed
US-8148380-B2 Antibacterial amide and sulfonamide substituted heterocyclic urea compounds CRESTONE, INC. (US) 2012-04-03 US disclosed
US-20120015941-A1 Antibacterial Amide and Sulfonamide Substituted Heterocyclic Urea Compounds CRESTONE, INC. (US) 2012-01-19 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-20120015941-A1 Antibacterial Amide and Sulfonamide Substituted Heterocyclic Urea Compounds NAAA, AADAC, RPSA LMNA 4293/4885HTT 1843/4885SMN1; SMN2 2356/4885

“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.