SCHEMBL23610046

SCHEMBL23610046

CC(O)(c1ccc(Cl)cc1)c1ccccn1

nearest known ligand 0.57

Predicted protein targets (top 15)

geneUniProtsupporting neighboursconfidence
MEN1 O00255 1/20 0.57
KMT2A Q03164 1/20 0.57
CYP19A1 P11511 9/20 0.50
L3MBTL1 Q9Y468 2/20 0.50
SMN1; SMN2 Q16637 1/20 0.50
CASR P41180 1/20 0.47
HDAC6 Q9UBN7 2/20 0.46
MDM2 Q00987 1/20 0.44
AHR P35869 1/20 0.43
TLR7 Q9NYK1 1/20 0.41
NPC1 O15118 1/20 0.40
AGTR1 P30556 1/20 0.40
OPRK1 P41145 1/20 0.40
KDM4E B2RXH2 1/20 0.40
PKM P14618 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
SCHEMBL23610056 1.00 MEN1 (0.57) MEN1KMT2ACYP19A1L3MBTL1SMN1; SMN2
SCHEMBL31143610 1.00 MEN1 (0.57) MEN1KMT2ACYP19A1L3MBTL1SMN1; SMN2
SCHEMBL31143781 1.00 MEN1 (0.57) MEN1KMT2ACYP19A1L3MBTL1SMN1; SMN2
SCHEMBL31143640 0.85 SMN1; SMN2 (0.57) MEN1KMT2AL3MBTL1SMN1; SMN2HDAC6
SCHEMBL23619158 0.85 SMN1; SMN2 (0.57) MEN1KMT2AL3MBTL1SMN1; SMN2HDAC6
SCHEMBL7559746 0.85 SMN1; SMN2 (0.57) MEN1KMT2AL3MBTL1SMN1; SMN2HDAC6
SCHEMBL11683866 0.85 CYP19A1 (0.49) MEN1KMT2ACYP19A1L3MBTL1SMN1; SMN2
SCHEMBL16132512 0.84 SMN1; SMN2 (0.52) MEN1KMT2ACYP19A1L3MBTL1SMN1; SMN2
SCHEMBL3045407 0.84 SMN1; SMN2 (0.67) CYP19A1L3MBTL1SMN1; SMN2AHRTLR7
SCHEMBL30040219 0.83 SMN1; SMN2 (0.50) MEN1KMT2AL3MBTL1SMN1; SMN2HDAC6

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
US-11130734-B2 Amino alcohol-boron-binol complex and method for preparing optically active amino alcohol derivative by using same MOLECULES & MATERIALS CO., LTD. (KR) 2021-09-28 US disclosed
US-11130734-B2 Amino alcohol-boron-binol complex and method for preparing optically active amino alcohol derivative by using same MOLECULES & MATERIALS CO., LTD. (KR) 2021-09-28 US disclosed
US-20210206719-A1 AMINO ALCOHOL-BORON-BINOL COMPLEX AND METHOD FOR PREPARING OPTICALLY ACTIVE AMINO ALCOHOL DERIVATIVE BY USING SAME MOLECULES & MATERIALS CO., LTD. (KR) 2021-07-08 US disclosed
US-20210206719-A1 AMINO ALCOHOL-BORON-BINOL COMPLEX AND METHOD FOR PREPARING OPTICALLY ACTIVE AMINO ALCOHOL DERIVATIVE BY USING SAME MOLECULES & MATERIALS CO., LTD. (KR) 2021-07-08 US disclosed
CN-113072486-A Amino alcohol-boron-binaphthol complex and preparation method of optically active amino alcohol derivative using same 分子与物质株式会社 2021-07-06 CN 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-11130734-B2 Amino alcohol-boron-binol complex and method for preparing optically active amino alcohol derivative by using same BCAT1, BCAT2, HBS1L MEN1 924/4885KMT2A 3665/4885CYP19A1 3214/4885
US-20210206719-A1 AMINO ALCOHOL-BORON-BINOL COMPLEX AND METHOD FOR PREPARING OPTICALLY ACTIVE AMINO ALCOHOL DERIVATIVE BY USING SAME BCAT1, BCAT2, HBS1L MEN1 1024/4885KMT2A 3481/4885CYP19A1 3408/4885

“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.