SCHEMBL1255010

SCHEMBL1255010

O=C(O)N(Cl)Cc1ccccc1

nearest known ligand 0.55

Predicted protein targets (top 17)

geneUniProtsupporting neighboursconfidence
CA12 O43570 1/20 0.55
CA9 Q16790 1/20 0.55
NPC1 O15118 3/20 0.50
RAB9A P51151 3/20 0.50
ALDH1A1 P00352 3/20 0.50
GLA P06280 1/20 0.50
HTT P42858 1/20 0.50
PAX8 Q06710 1/20 0.50
SMN1; SMN2 Q16637 1/20 0.50
LMNA P02545 1/20 0.48
NPSR1 Q6W5P4 1/20 0.47
TSHR P16473 2/20 0.46
CES2 O00748 1/20 0.46
CES1 P23141 1/20 0.46
AKR1B1 P15121 1/20 0.46
KMT2A Q03164 3/20 0.46
MEN1 O00255 2/20 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
SCHEMBL3837997 0.85 CA12 (0.55) CA12CA9NPC1RAB9AALDH1A1
SCHEMBL23805051 0.85 CA12 (0.50) CA12CA9NPC1RAB9AALDH1A1
SCHEMBL17710407 0.85 CA12 (0.50) CA12CA9NPC1RAB9AALDH1A1
SCHEMBL28062695 0.82 ALDH1A1 (0.52) RAB9AALDH1A1HTTTSHRKMT2A
SCHEMBL28949040 0.81 NPC1 (0.52) CA12CA9NPC1RAB9AALDH1A1
SCHEMBL27639509 0.81 NPC1 (0.47) CA12CA9NPC1RAB9AALDH1A1
SCHEMBL8380163 0.81 ALDH1A1 (0.49) CA12CA9NPC1RAB9AALDH1A1
SCHEMBL11064075 0.80 KMT2A (0.56) CA12CA9NPC1RAB9AALDH1A1
SCHEMBL17333394 0.78 NPC1 (0.53) CA12CA9NPC1RAB9AALDH1A1
SCHEMBL5144630 0.77 MEN1 (0.58) ALDH1A1KMT2AMEN1

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 30 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-11732005-B2 Peptidomimetic proteasome inhibitors CORNELL UNIVERSITY (US) 2023-08-22 US disclosed
CN-114174281-A Degradation agent for cyclin dependent kinase 7(CDK7) and use thereof 达纳-法伯癌症研究公司 2022-03-11 CN disclosed
US-20220056073-A1 PEPTIDOMIMETIC PROTEASOME INHIBITORS UNIV CORNELL (US) 2022-02-24 US disclosed
US-11203613-B2 Peptidomimetic proteasome inhibitors CORNELL UNIVERSITY 2021-12-21 US disclosed
US-20200317729-A1 PEPTIDOMIMETIC PROTEASOME INHIBITORS CORNELL UNIVERSITY 2020-10-08 US disclosed
EP-3694605-A1 PEPTIDOMIMETIC PROTEASOME INHIBITORS Cornell University (US) 2020-08-19 EP disclosed
WO-2019075252-A1 PEPTIDOMIMETIC PROTEASOME INHIBITORS CORNELL UNIVERSITY (US) 2019-04-18 WO disclosed
EP-2576569-A1 SYNTHETIC PROCESS FOR THE MANUFACTURE OF ECTEINASCIDIN COMPOUNDS Pharma Mar S.A. (ES) 2013-04-10 EP disclosed
WO-2011147828-A1 SYNTHETIC PROCESS FOR THE MANUFACTURE OF ECTEINASCIDIN COMPOUNDS PHARMA MAR, S.A. (ES) 2011-12-01 WO disclosed
US-7884182-B2 For assembling oligopeptide intermediates in chemical ligation reaction; prevents self-ligation; solid phase synthesis AMYLIN PHARMACEUTICALS, INC. (US) 2011-02-08 US disclosed
EP-1511760-A2 CARBOXY PROTECTION STRATEGIES FOR ACIDIC C-TERMINAL AMINO ACIDS IN CHEMICAL LIGATION OF OLIGOPEPTIDES Geneprot, Inc. (CH) 2005-03-09 EP disclosed
EP-0984925-B1 COMPOUNDS, PREPARATION AND USE FOR TRANSFERRING NUCLEIC ACIDS INTO CELLS AVENTIS PHARMA SA (FR) 2004-12-08 EP disclosed
EP-1456225-A2 EXTENDED NATIVE CHEMICAL LIGATION OF THREE OR MORE PEPTIDE FRAGMENTS Geneprot, Inc. (CH) 2004-09-15 EP disclosed
WO-2003042235-A9 EXTENDED NATIVE CHEMICAL LIGATION OF THREE OR MORE PEPTIDE FRAGMENTS GENEPROT INC (CH) 2004-07-29 WO disclosed
WO-2004007661-A2 CARBOXY PROTECTION STRATEGIES FOR ACIDIC C-TERMINAL AMINO ACIDS IN CHEMICAL LIGATION OF OLIGOPEPTIDES GENEPROT, INC. (CH) 2004-01-22 WO disclosed
WO-2003106615-A2 POST-CLEAVAGE SULFUR DEPROTECTION FOR CONVERGENT PROTEIN SYNTHESIS BY CHEMICAL LIGATION GENEPROT, INC. (CH) 2003-12-24 WO disclosed
WO-2003042235-A2 EXTENDED NATIVE CHEMICAL LIGATION OF THREE OR MORE PEPTIDE FRAGMENTS GENEPROT, INC. (CH) 2003-05-22 WO disclosed
US-6300321-B1 LIPOPOLYAMINES AVENTIS PHARMA S.A. (FR) 2001-10-09 US disclosed
EP-0984925-A1 COMPOUNDS, PREPARATION AND USE FOR TRANSFERRING NUCLEIC ACIDS INTO CELLS Aventis Pharma S.A. (FR) 2000-03-15 EP disclosed
WO-1998054130-A1 COMPOUNDS, PREPARATION AND USE FOR TRANSFERRING NUCLEIC ACIDS INTO CELLS RHONE-POULENC RORER S.A. (FR) 1998-12-03 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 (4 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-20200317729-A1 PEPTIDOMIMETIC PROTEASOME INHIBITORS PSMB1, PSMB3, PSMB11 CA12 4562/4885CA9 4312/4885NPC1 4062/4885
US-20220056073-A1 PEPTIDOMIMETIC PROTEASOME INHIBITORS PSMB1, PSMB3, PSMB11 CA12 4556/4885CA9 4300/4885NPC1 4075/4885
US-11203613-B2 Peptidomimetic proteasome inhibitors PSMB1, PSMB3, PSMB11 CA12 4562/4885CA9 4312/4885NPC1 4062/4885
US-11732005-B2 Peptidomimetic proteasome inhibitors PSMB1, PSMB3, PSMB11 CA12 4556/4885CA9 4300/4885NPC1 4075/4885

“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.