SCHEMBL29131265

SCHEMBL29131265

CCOP(=O)(CSc1ccc(Cl)cc1)OCC

nearest known ligand 0.54

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
MEN1 O00255 3/20 0.54
KMT2A Q03164 3/20 0.54
MAPT P10636 3/20 0.39
HPGD P15428 3/20 0.39
LMNA P02545 1/20 0.39
SMN1; SMN2 Q16637 3/20 0.39
ALDH1A1 P00352 3/20 0.39
KDM4E B2RXH2 2/20 0.39
PKM P14618 1/20 0.39
KCNH2 Q12809 1/20 0.39
HTT P42858 1/20 0.38
HSD17B10 Q99714 1/20 0.38
TDP1 Q9NUW8 1/20 0.38
L3MBTL1 Q9Y468 1/20 0.38
TSHR P16473 1/20 0.38
RAB9A P51151 2/20 0.36
NPC1 O15118 2/20 0.36
DAO P14920 1/20 0.36
POLB P06746 1/20 0.36
MMP2 P08253 1/20 0.36

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
SCHEMBL17754399 0.84 KCNH2 (0.40) MEN1KMT2AMAPTHPGDALDH1A1
SCHEMBL30810994 0.83 MAOA (0.40) MEN1KMT2ALMNASMN1; SMN2ALDH1A1
SCHEMBL31248444 0.83 CA2 (0.40) MEN1KMT2AMAPTKCNH2TSHR
SCHEMBL11432311 0.83 ALDH1A1 (0.39) MEN1KMT2ALMNASMN1; SMN2ALDH1A1
SCHEMBL722868 0.82 KCNH2 (0.58) MEN1KMT2AMAPTHPGDALDH1A1
SCHEMBL1331369 0.82 KCNH2 (0.58) MEN1KMT2AMAPTHPGDALDH1A1
SCHEMBL29131330 0.81 MTNR1A (0.42) KMT2AMAPTSMN1; SMN2ALDH1A1KDM4E
SCHEMBL31389228 0.81 KCNH2 (0.41) MEN1KMT2AMAPTLMNAKCNH2
SCHEMBL31248445 0.81 KCNH2 (0.41) MEN1KMT2AMAPTLMNAKCNH2
SCHEMBL31327270 0.78 CA1 (0.54) MEN1KMT2AMAPTHPGDLMNA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-117303992-A Preparation method of polyfunctional group substituted chiral sulfoxide compound 厦门大学 2023-12-29 CN claimed
WO-2025133217-A1 COMPOUNDS FLINDR THERAPEUTICS B. V. (NL) 2025-06-26 WO disclosed
EP-4543859-A1 3-(SULPHONYL OR SULFONIMIDOYL)PROP-2-EN-1-YL]-2-OXO-1,2-DIHYDROPYRIDINE-3-CARBOXAMIDE DERIVATIVES Flindr Therapeutics B.V. (NL) 2025-04-30 EP disclosed
US-12234207-B2 Halo-(3-(phenylsulfonyl)prop-1-enyl)pyridine derivative and use thereof CUREVERSE INCORPORATED (KR) 2025-02-25 US disclosed
CN-112930345-B Novel halo- (3- (benzenesulfonyl) prop-1-ene) pyridine derivatives and use thereof 库尔维斯株式会社 2024-09-24 CN disclosed
CN-117303992-A Preparation method of polyfunctional group substituted chiral sulfoxide compound 厦门大学 2023-12-29 CN disclosed
WO-2023249490-A1 3-(SULPHONYL OR SULFONIMIDOYL)PROP-2-EN-1-YL]-2-OXO-1,2-DIHYDROPYRIDINE-3-CARBOXAMIDE DERIVATIVES IMMAGENE B.V. (NL) 2023-12-28 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 (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-12234207-B2 Halo-(3-(phenylsulfonyl)prop-1-enyl)pyridine derivative and use thereof KEAP1, NFE2L2, NQO1 MEN1 4692/4885KMT2A 2452/4885MAPT 2326/4885

“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.