SCHEMBL2222173

SCHEMBL2222173

O=C1CCC(C(=O)Nc2ccccc2)N1

nearest known ligand 0.65

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
POLB P06746 2/20 0.63
MEN1 O00255 2/20 0.62
KMT2A Q03164 2/20 0.62
SMN1; SMN2 Q16637 1/20 0.62
DDB1 Q16531 1/20 0.60
CRBN Q96SW2 1/20 0.60
NAMPT P43490 2/20 0.51
PARP1 P09874 2/20 0.50
HPGD P15428 1/20 0.50
HDAC3 O15379 4/20 0.49
HDAC11 Q96DB2 4/20 0.49
HDAC6 Q9UBN7 4/20 0.49
HDAC1 Q13547 3/20 0.49
HDAC2 Q92769 3/20 0.49
HDAC10 Q969S8 3/20 0.49
HDAC8 Q9BY41 3/20 0.49
GAA P10253 1/20 0.49
MAPT P10636 1/20 0.49
GFER P55789 1/20 0.49
HPGDS O60760 1/20 0.48

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
SCHEMBL2222163 1.00 POLB (0.63) POLBMEN1KMT2ASMN1; SMN2DDB1
SCHEMBL10743630 0.86 POLB (0.62) POLBMEN1KMT2ASMN1; SMN2DDB1
SCHEMBL9530359 0.86 POLB (0.62) POLBMEN1KMT2ASMN1; SMN2DDB1
SCHEMBL13777929 0.84 POLB (0.64) POLBMEN1KMT2ASMN1; SMN2NAMPT
SCHEMBL30597986 0.83 NPSR1 (0.58) POLBMEN1KMT2ASMN1; SMN2PARP1
SCHEMBL30434482 0.83 POLB (0.55) POLBMEN1KMT2ASMN1; SMN2PARP1
SCHEMBL2334270 0.83 MEN1 (0.61) POLBMEN1KMT2ASMN1; SMN2NAMPT
SCHEMBL13777928 0.83 NPSR1 (0.58) POLBMEN1KMT2ASMN1; SMN2PARP1
SCHEMBL29549442 0.83 MEN1 (0.61) POLBMEN1KMT2ASMN1; SMN2NAMPT
SCHEMBL28103666 0.83 POLB (0.55) POLBMEN1KMT2ASMN1; SMN2PARP1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-12564583-B2 Small molecules against cereblon to enhance effector T cell function Lee Moffitt Cancer Center and Research Institute, Inc. (US) 2026-03-03 US disclosed
US-20230226035-A1 SMALL MOLECULES AGAINST CEREBLON TO ENHANCE EFFECTOR T CELL FUNCTION H. LEE MOFFITT CANCER CENTER AND RESEARCH INSTITUTE, INC. 2023-07-20 US disclosed
CN-109153644-B Small molecules against CEREBLON to enhance effector T cell function H·李·莫菲特癌症中心研究有限公司 2022-10-21 CN disclosed
US-11395820-B2 Small molecules against cereblon to enhance effector t cell function H. LEE MOFFITT CANCER CENTER AND RESEARCH INSTITUTE, INC. (US) 2022-07-26 US disclosed
US-20210177825-A1 SMALL MOLECULES AGAINST CEREBLON TO ENHANCE EFFECTOR T CELL FUNCTION H. LEE MOFFITT CANCER CENTER AND RESEARCH INSTITUTE, INC. 2021-06-17 US disclosed
EP-3429996-A1 SMALL MOLECULES AGAINST CEREBLON TO ENHANCE EFFECTOR T CELL FUNCTION H. Lee Moffitt Cancer Center And Research Institute, Inc. (US) 2019-01-23 EP disclosed
CN-109153644-A SMALL MOLECULES AGAINST CEREBLON TO ENHANCE EFFECTOR T CELL FUNCTION H·李·莫菲特癌症中心研究有限公司 2019-01-04 CN disclosed
WO-2017161119-A1 SMALL MOLECULES AGAINST CEREBLON TO ENHANCE EFFECTOR T CELL FUNCTION H. LEE MOFFITT CANCER CENTER & RESEARCH INSTITUTE, INC. (US) 2017-09-21 WO disclosed
US-8716520-B2 Method of resolution of (RS)- 1,1′-BI-2-naphthol for obtaining enantiomeric pure I.E. (S)-(−)-1,1′-BI-2-naphthol and/or (R)-(+)-1,1′-BI-2-naphthol via co-crystal formation with optically active derivatives of γ-amino acids LUPIN LIMITED (IN) 2014-05-06 US disclosed
US-20120316361-A1 METHOD OF RESOLUTION OF (RS)- 1,1'-BI-2-NAPHTHOL FOR OBTAINING ENANTIOMERIC PURE I.E. (S)-(-)-1,1'-BI-2-NAPHTHOL AND/OR (R)-(+)-1,1'-BI-2-NAPHTHOL VIA CO-CRYSTAL FORMATION WITH OPTICALLY ACTIVE DERIVATIVES OF y -AMINO ACIDS LUPIN LIMITED (IN) 2012-12-13 US disclosed
WO-2011086566-A1 METHOD OF RESOLUTION OF (RS) - 1, 1 ' - BI - 2 - NAPHTHOL FOR OBTAINING ENANTIOMERIC PURE I.E. (S) - (-) \" 1, 1 ' \"BI - 2 -NAPHTHOL AND/OR (R) - ( ) - 1, 1 ' - BI - 2 - NAPHTHOL VIA CO - CRYSTAL FORMATION WITH OPTICALLY ACTIVE DERIVATIVES OF GAMMA -AMINO ACIDS LUPIN LIMITED (IN) 2011-07-21 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 (5 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-20120316361-A1 METHOD OF RESOLUTION OF (RS)- 1,1'-BI-2-NAPHTHOL FOR OBTAINING ENANTIOMERIC PURE I.E. (S)-(-)-1,1'-BI-2-NAPHTHOL AND/OR (R)-(+)-1,1'-BI-2-NAPHTHOL VIA CO-CRYSTAL FORMATION WITH OPTICALLY ACTIVE DERIVATIVES OF y -AMINO ACIDS RRS1, RER1, QTRT1 POLB 1375/4885MEN1 1947/4885KMT2A 4648/4885
US-12564583-B2 Small molecules against cereblon to enhance effector T cell function CRBN, CD4, ICOS POLB 4576/4885MEN1 3857/4885KMT2A 3331/4885
US-11395820-B2 Small molecules against cereblon to enhance effector t cell function CD4, GZMB, CRBN POLB 4464/4885MEN1 1005/4885KMT2A 3183/4885
US-20230226035-A1 SMALL MOLECULES AGAINST CEREBLON TO ENHANCE EFFECTOR T CELL FUNCTION CD4, CRBN, GZMB POLB 4402/4885MEN1 738/4885KMT2A 3074/4885
US-20210177825-A1 SMALL MOLECULES AGAINST CEREBLON TO ENHANCE EFFECTOR T CELL FUNCTION CD4, GZMB, CRBN POLB 4464/4885MEN1 1005/4885KMT2A 3183/4885

“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.