SCHEMBL3483641

SCHEMBL3483641

O=S(=O)(Cc1ccccc1SS)c1ccccc1

nearest known ligand 0.44

Predicted protein targets (top 17)

geneUniProtsupporting neighboursconfidence
PSIP1 O75475 1/20 0.44
SMN1; SMN2 Q16637 4/20 0.41
NPC1 O15118 2/20 0.41
RAB9A P51151 2/20 0.41
MAPT P10636 1/20 0.40
MPO P05164 1/20 0.40
POLB P06746 2/20 0.39
TSHR P16473 1/20 0.38
HSD17B10 Q99714 1/20 0.38
L3MBTL1 Q9Y468 1/20 0.37
LMNA P02545 2/20 0.36
ALDH1A1 P00352 1/20 0.36
HSD11B1 P28845 3/20 0.36
HTR6 P50406 1/20 0.35
MMP3 P08254 1/20 0.35
MMP8 P22894 1/20 0.35
MMP13 P45452 1/20 0.35

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
SCHEMBL3483640 0.85 PSIP1 (0.47) PSIP1SMN1; SMN2NPC1RAB9AMAPT
SCHEMBL3483705 0.78 LMNA (0.35) LMNA
SCHEMBL11922695 0.73 PSIP1 (0.61) PSIP1SMN1; SMN2NPC1RAB9AMAPT
SCHEMBL2808506 0.72 PSIP1 (0.54) PSIP1SMN1; SMN2NPC1RAB9AMAPT
SCHEMBL1283787 0.72 PSIP1 (0.48) PSIP1SMN1; SMN2NPC1RAB9AMAPT
SCHEMBL4067607 0.72 PSIP1 (0.48) PSIP1SMN1; SMN2NPC1RAB9AMAPT
SCHEMBL1714597 0.72 PSIP1 (0.48) PSIP1SMN1; SMN2NPC1RAB9AMAPT
SCHEMBL3147023 0.72 PSIP1 (0.48) PSIP1SMN1; SMN2NPC1RAB9AMAPT
SCHEMBL14272117 0.72 PSIP1 (0.48) PSIP1SMN1; SMN2NPC1RAB9AMAPT
SCHEMBL4959331 0.72 PSIP1 (0.48) PSIP1SMN1; SMN2NPC1RAB9AMAPT

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7851646-B2 formed by reacting aryl sulfur compound with halogen and fluoro salt to form arylsulfur halotetrafluoride which is reacted with fluoride source to form target arylsulfur pentafluoride; for production of fungicides, herbicides, and insecticides IM&T RESEARCH, INC. (US) 2010-12-14 US disclosed
US-20100076215-A9 Process for Producing Arylsulfur Pentafluorides IM&T RESEARCH, INC. (US) 2010-03-25 US disclosed
US-20090287024-A1 Process for Producing Arylsulfur Pentafluorides IM&T RESEARCH, INC. (US) 2009-11-19 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 (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-20090287024-A1 Process for Producing Arylsulfur Pentafluorides PFAS, MPST, ARSA PSIP1 313/4885SMN1; SMN2 2262/4885NPC1 2716/4885
US-20100076215-A9 Process for Producing Arylsulfur Pentafluorides PFAS, MPST, ARSA PSIP1 313/4885SMN1; SMN2 2262/4885NPC1 2716/4885

“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.