SCHEMBL5491920

SCHEMBL5491920

C=C(CS(=O)(=O)c1ccccc1)C(=O)O

nearest known ligand 0.56

Predicted protein targets (top 15)

geneUniProtsupporting neighboursconfidence
HSD11B1 P28845 8/20 0.56
MMP2 P08253 1/20 0.52
MMP7 P09237 1/20 0.52
MMP14 P50281 1/20 0.52
POLB P06746 2/20 0.50
KMT2A Q03164 1/20 0.50
ALDH1A1 P00352 2/20 0.49
SMN1; SMN2 Q16637 1/20 0.49
TP53 P04637 1/20 0.49
HTT P42858 1/20 0.49
HSD17B10 Q99714 1/20 0.49
PSIP1 O75475 1/20 0.48
CA12 O43570 1/20 0.46
CA2 P00918 1/20 0.46
CA9 Q16790 1/20 0.46

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
SCHEMBL24106342 0.83 MAPT (0.53) HSD11B1MMP2MMP7MMP14POLB
Hydrochloric Acid SCHEMBL30116899 0.83 HSD11B1 (0.51) HSD11B1MMP2MMP7MMP14POLB
SCHEMBL8572063 0.83 ALDH1A1 (0.61) HSD11B1POLBKMT2AALDH1A1TP53
SCHEMBL3182773 0.80 HSD11B1 (0.53) HSD11B1MMP2MMP7MMP14POLB
SCHEMBL194095 0.80 HSD11B1 (0.53) HSD11B1MMP2MMP7MMP14POLB
SCHEMBL6795476 0.80 PRMT1 (0.61) POLBKMT2ASMN1; SMN2HTTCA12
SCHEMBL6789657 0.79 NPC1 (0.56) HSD11B1MMP2MMP7MMP14ALDH1A1
SCHEMBL7210507 0.79 HTT (0.58) HSD11B1POLBKMT2AALDH1A1SMN1; SMN2
SCHEMBL270706 0.79 MMP2 (0.77) HSD11B1MMP2MMP7MMP14POLB
SCHEMBL5080063 0.78 HSD11B1 (0.58) HSD11B1POLBKMT2AALDH1A1TP53

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-109776324-A Homoallyltrifluoromethyl compound and preparation method thereof 南京工业大学 2019-05-21 CN claimed
US-12435027-B1 Preparation method of N-butenyl amide compounds ZHEJIANG NORMAL UNIVERSITY (CN) 2025-10-07 US disclosed
CN-109776324-A Homoallyltrifluoromethyl compound and preparation method thereof 南京工业大学 2019-05-21 CN disclosed
US-7306893-B2 Intermediate layer contains a unsaturated polymer having a carboxylic acid group in the side chain, which has specific reaction between the support and the photosensitive layer to promot adhesion strength; improve printing durability, chemical resistance; laser recording, photothermography FUJIFILM CORPORATION (JP) 2007-12-11 US disclosed
US-20050048399-A1 Intermediate layer contains a unsaturated polymer having a carboxylic acid group in the side chain, which has specific reaction between the support and the photosensitive layer to promot adhesion strength; improve printing durability, chemical resistance; laser recording, photothermography FUJI PHOTO FILM CO., LTD. 2005-03-03 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-12435027-B1 Preparation method of N-butenyl amide compounds BBOX1, NAT1, AADAC HSD11B1 3155/4885MMP2 3931/4885MMP7 4506/4885

“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.