SCHEMBL6211532

SCHEMBL6211532

CC(C)(C)NC(=S)N[C@H](CO)Cc1cccc([N+](=O)[O-])c1

nearest known ligand 0.44

Predicted protein targets (top 15)

geneUniProtsupporting neighboursconfidence
LMNA P02545 5/20 0.44
SMN1; SMN2 Q16637 4/20 0.42
HPGD P15428 2/20 0.42
THRB P10828 1/20 0.42
ALOX12 P18054 1/20 0.42
ALDH1A1 P00352 5/20 0.42
KMT2A Q03164 4/20 0.42
MEN1 O00255 3/20 0.42
GAA P10253 2/20 0.42
L3MBTL1 Q9Y468 2/20 0.41
HTT P42858 2/20 0.41
MAPT P10636 2/20 0.41
TSHR P16473 1/20 0.41
POLB P06746 1/20 0.41
MME P08473 1/20 0.40

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
SCHEMBL6210731 1.00 LMNA (0.44) LMNASMN1; SMN2HPGDTHRBALOX12
SCHEMBL6210717 1.00 LMNA (0.44) LMNASMN1; SMN2HPGDTHRBALOX12
SCHEMBL27561727 0.82 LMNA (0.48) LMNASMN1; SMN2HPGDTHRBALOX12
SCHEMBL27501950 0.82 LMNA (0.48) LMNASMN1; SMN2HPGDTHRBALOX12
SCHEMBL6190987 0.81 LMNA (0.52) LMNASMN1; SMN2HPGDALDH1A1GAA
SCHEMBL6193183 0.81 LMNA (0.52) LMNASMN1; SMN2HPGDALDH1A1GAA
SCHEMBL27503054 0.81 LMNA (0.52) LMNASMN1; SMN2HPGDALDH1A1GAA
SCHEMBL3222312 0.80 MAPT (0.52) LMNASMN1; SMN2HPGDALDH1A1L3MBTL1
SCHEMBL3222299 0.80 MAPT (0.52) LMNASMN1; SMN2HPGDALDH1A1L3MBTL1
SCHEMBL29643038 0.80 MAPT (0.52) LMNASMN1; SMN2HPGDALDH1A1L3MBTL1

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-1299365-B1 2-AMINOTHIAZOLINE DERIVATIVES AND THEIR USE AS NO-SYNTHASE INHIBITORS AVENTIS PHARMA SA (FR) 2005-09-28 EP disclosed
US-6699895-B2 CYCLIZING THE TERT-BUTYL-THIOUREA DERIVATIVE TO FORM THE END PRODUCT AVENTIS PHARMA S.A. (FR) 2004-03-02 US disclosed
US-20020198243-A1 2-aminothiazoline derivatives and process for preparing the same CARRY JEAN-CHRISTOPHE (FR) 2002-12-26 US disclosed
US-20020187987-A1 Use of 2-aminothiazoline derivatives as inhibitors of inducible NO-synthase CARRY JEAN-CHRISTOPHE (FR) 2002-12-12 US disclosed
US-6451821-B1 ADMINISTERING TO A PATIENT A THERAPEUTICALLY EFFECTIVE AMOUNT OF 2-AMINOTHIAZOLINE DERIVATIVES FOR TREATING OR PREVENTING DISEASE CONDITIONS ASSOCIATED WITH AN ABNORMAL PRODUCTION OF NITRIC OXIDE(NO) AVENTIS PHARMA S.A. (FR) 2002-09-17 US disclosed
US-20020022631-A1 Use of 2-aminothiazoline derivatives as inhibitors of inducible no-synthase AVENTIS PHARMA S.A. (FR) 2002-02-21 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 (3 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-20020022631-A1 Use of 2-aminothiazoline derivatives as inhibitors of inducible no-synthase NOS2, NOS3, NOS1 LMNA 4068/4885SMN1; SMN2 4144/4885HPGD 109/4885
US-20020198243-A1 2-aminothiazoline derivatives and process for preparing the same NOS3, TH, CBR1 LMNA 3890/4885SMN1; SMN2 2862/4885HPGD 175/4885
US-20020187987-A1 Use of 2-aminothiazoline derivatives as inhibitors of inducible NO-synthase NOS2, NOS3, NOS1 LMNA 4084/4885SMN1; SMN2 4243/4885HPGD 90/4885

“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.