SCHEMBL332185

SCHEMBL332185

NC(CS)C(=O)c1cccs1

nearest known ligand 0.50

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CES2 O00748 2/20 0.50
CES1 P23141 2/20 0.50
KEAP1 Q14145 1/20 0.50
KMT2A Q03164 3/20 0.49
MAPT P10636 1/20 0.49
ADAM17 P78536 1/20 0.49
ATM Q13315 1/20 0.49
RAB9A P51151 4/20 0.48
NPC1 O15118 3/20 0.48
ALDH1A1 P00352 2/20 0.48
MEN1 O00255 2/20 0.48
POLB P06746 2/20 0.48
LMNA P02545 1/20 0.48
DAO P14920 1/20 0.47
HPGD P15428 2/20 0.46
SMN1; SMN2 Q16637 1/20 0.46
GSK3B P49841 1/20 0.46
CYP2C19 P33261 2/20 0.44
CYP2D6 P10635 1/20 0.44
CYP2C9 P11712 1/20 0.44

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
SCHEMBL332184 1.00 CES2 (0.50) CES2CES1KEAP1KMT2AMAPT
SCHEMBL30944840 0.93 DAO (0.44) CES2CES1KEAP1KMT2AMAPT
SCHEMBL8298426 0.82 TSHR (0.55) CES2CES1KEAP1KMT2AMAPT
Hydrochloric Acid SCHEMBL4126481 0.81 TSHR (0.54) CES2CES1KEAP1KMT2AMAPT
SCHEMBL13116466 0.79 TSHR (0.49) CES2CES1KEAP1KMT2AMAPT
SCHEMBL11245259 0.79 CYP2C19 (0.53) CES2CES1KEAP1KMT2AMAPT
SCHEMBL10761013 0.76 CES2 (0.55) CES2CES1KEAP1KMT2AMAPT
Hydrochloric Acid SCHEMBL10810413 0.74 RAB9A (0.53) CES2CES1KEAP1KMT2AMAPT
SCHEMBL13116484 0.73 ALDH1A1 (0.49) CES2CES1KEAP1KMT2AMAPT
Hydrochloric Acid SCHEMBL3418543 0.73 DAO (0.53) CES2CES1KEAP1KMT2AMAPT

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2374480-A2 Mutli-drug ligand conjugates Endocyte, Inc. (US) 2011-10-12 EP claimed
US-20080124765-A1 EXPRESSION OF FUNCTIONAL ANTIBODY FRAGMENTS GENENTECH, INC. (US) 2008-05-29 US claimed
JP-3951062-B2 2007-08-01 JP claimed
US-5648237-A Expression of functional antibody fragments GENENTECH, INC. (US) 1997-07-15 US claimed
EP-0604580-A1 EXPRESSION IN E. COLI OF ANTIBODY FRAGMENTS HAVING AT LEAST A CYSTEINE PRESENT AS A FREE THIOL, USE FOR THE PRODUCTION OF BIFUNCTIONAL F(ab') 2? ANTIBODIES GENENTECH, INC. (US) 1994-07-06 EP claimed
WO-1993006217-A1 EXPRESSION IN E. COLI OF ANTIBODY FRAGMENTS HAVING AT LEAST A CYSTEINE PRESENT AS A FREE THIOL, USE FOR THE PRODUCTION OF BIFUNCTIONAL F(ab')2 ANTIBODIES GENENTECH, INC. (US) 1993-04-01 WO claimed
CN-122094701-A TLR3 binding bicyclic peptide ligands 2026-05-26 CN disclosed
EP-4736892-A2 METHODS FOR PREPARING PATHOGEN-INACTIVATED WHOLE BLOOD Cerus Corporation (US) 2026-05-06 EP disclosed
EP-3852817-B1 METHODS FOR PREPARING PATHOGEN-INACTIVATED WHOLE BLOOD CERUS CORP (US) 2026-02-18 EP disclosed
US-20260034277-A1 SYSTEMS AND METHODS FOR PATHOGEN INACTIVATION OF BLOOD PRODUCTS CERUS CORP (US) 2026-02-05 US disclosed
US-20250282827-A1 LIPIDATED POLYMYXIN ANALOGUES AUCKLAND UNISERVICES LTD (NZ) 2025-09-11 US disclosed
US-20250270610-A1 Improving the Efficiency of PAL-Catalyzed Protein Ligation By A Cascade Enzymatic Scheme NANYANG TECHNOLOGICAL UNIVERSITY (SG) 2025-08-28 US disclosed
WO-2025007126-A9 COMPOSITIONS COMPRISING NEURAL PRECURSOR CELL EXPRESSED, DEVELOPMENTALLY DOWN-REGULATED 9 (NEDD9)-BINDING PEPTIDES AND METHODS OF USE THEREOF THE BRIGHAM AND WOMEN'S HOSPITAL, INC. (US) 2025-04-10 WO disclosed
EP-0604580-A1 EXPRESSION IN E. COLI OF ANTIBODY FRAGMENTS HAVING AT LEAST A CYSTEINE PRESENT AS A FREE THIOL, USE FOR THE PRODUCTION OF BIFUNCTIONAL F(ab') 2? ANTIBODIES GENENTECH, INC. (US) 1994-07-06 EP disclosed
WO-1993006217-A1 EXPRESSION IN E. COLI OF ANTIBODY FRAGMENTS HAVING AT LEAST A CYSTEINE PRESENT AS A FREE THIOL, USE FOR THE PRODUCTION OF BIFUNCTIONAL F(ab')2 ANTIBODIES GENENTECH, INC. (US) 1993-04-01 WO disclosed
EP-0487648-A4 ODOR-MASKED AND STABILIZED COMPOSITIONS FOR TREATING KERATINOUS TISSUE, SKIN CONDITIONS, AND PROMOTING WOUND HEALING 1993-03-31 EP disclosed
EP-0487648-A1 ODOR-MASKED AND STABILIZED COMPOSITIONS FOR TREATING KERATINOUS TISSUE, SKIN CONDITIONS, AND PROMOTING WOUND HEALING JOHN MORRIS CO., INC. (US) 1992-06-03 EP disclosed
US-5059421-A Stable protein-liposome conjugate exhibiting an absence of aggregation THE LIPOSOME COMPANY, INC. (US) 1991-10-22 US disclosed
WO-1991002538-A1 ODOR-MASKED AND STABILIZED COMPOSITIONS FOR TREATING KERATINOUS TISSUE, SKIN CONDITIONS, AND PROMOTING WOUND HEALING JOHN MORRIS CO., INC. (US) 1991-03-07 WO disclosed
WO-1991000289-A2 TARGETED LIPOSOMES AND METHODS FOR LIPOSOME-PROTEIN COUPLING THE LIPOSOME COMPANY, INC. (US) 1991-01-10 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 (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-20260034277-A1 SYSTEMS AND METHODS FOR PATHOGEN INACTIVATION OF BLOOD PRODUCTS PRF1, CFD, F5 CES2 3283/4885CES1 2462/4885KEAP1 604/4885
US-20250282827-A1 LIPIDATED POLYMYXIN ANALOGUES PHOSPHO1, PCTP, PTMS CES2 4560/4885CES1 2778/4885KEAP1 3066/4885
US-20250270610-A1 Improving the Efficiency of PAL-Catalyzed Protein Ligation By A Cascade Enzymatic Scheme QPCT, GLUL, QPCTL CES2 2879/4885CES1 1561/4885KEAP1 1131/4885

“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.