SCHEMBL440968

SCHEMBL440968

CC(N)(CSSCC(C)(N)C(=O)O)C(=O)O

nearest known ligand 0.48

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
NOS2 P35228 5/20 0.48
NOS1 P29475 3/20 0.48
NOS3 P29474 1/20 0.48
GGT1 P19440 1/20 0.46
ARG1 P05089 1/20 0.42
ARG2 P78540 1/20 0.42
BLM P54132 2/20 0.41
ALDH1A1 P00352 4/20 0.37
MEN1 O00255 2/20 0.37
CYP1A2 P05177 2/20 0.37
KMT2A Q03164 2/20 0.37
KDM4E B2RXH2 2/20 0.37
USP2 O75604 1/20 0.37
EGFR P00533 1/20 0.37
FYN P06241 1/20 0.37
POLB P06746 1/20 0.37
CYP3A4 P08684 1/20 0.37
GAA P10253 1/20 0.37
MAPT P10636 1/20 0.37
HPGD P15428 1/20 0.37

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
SCHEMBL5517028 1.00 NOS2 (0.48) NOS2NOS1NOS3GGT1ARG1
SCHEMBL5518580 1.00 NOS2 (0.48) NOS2NOS1NOS3GGT1ARG1
Hydrochloric Acid SCHEMBL30568703 0.97 NOS2 (0.52) NOS2NOS1NOS3GGT1ARG1
Hydrochloric Acid SCHEMBL5520977 0.97 NOS2 (0.52) NOS2NOS1NOS3GGT1ARG1
Hydrochloric Acid SCHEMBL5520982 0.97 NOS2 (0.52) NOS2NOS1NOS3GGT1ARG1
SCHEMBL6835164 0.82 KIF11 (0.41) NOS2NOS1NOS3GGT1ARG1
SCHEMBL1667369 0.82 KIF11 (0.41) NOS2NOS1NOS3GGT1ARG1
SCHEMBL3703131 0.82 KIF11 (0.41) NOS2NOS1NOS3GGT1ARG1
SCHEMBL7281359 0.82
SCHEMBL7281364 0.82

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20070010689-A1 Optically active 3,3'-dithiobis(2-amino-2methylpropionic acid) derivative and process for producing optically active 2-amino-3-mercapto-2-methylpropionic acid derivative KANEKA CORPORATION (JP) 2007-01-11 US claimed
EP-1666458-A1 OPTICALLY ACTIVE 3,3 -DITHIOBIS(2-AMINO-2-METHYLPROPIONI C ACID) DERIVATIVE AND PROCESS FOR PRODUCING OPTICALLY ACTIVE 2-AMINO-3-MERCAPTO-2-METHYL-PROPIONIC ACID DERIVATIVE KANEKA CORPORATION (JP) 2006-06-07 EP claimed
EP-1144613-B2 METHODS FOR MAKING PROTEINS CONTAINING FREE CYSTEINE RESIDUES BOLDER BIOTECHNOLOGY INC (US) 2020-05-06 EP disclosed
US-20170362626-A1 METHODS FOR MAKING PROTEINS CONTAINING FREE CYSTEINE RESIDUES BOLDER BIOTECHNOLOGY, INC. 2017-12-21 US disclosed
US-20160244798-A1 METHODS FOR MAKING PROTEINS CONTAINING FREE CYSTEINE RESIDUES BOLDER BIOTECHNOLOGY, INC. 2016-08-25 US disclosed
EP-2305804-B1 MonoPEGylated human growth hormone BOLDER BIOTECHNOLOGY INC (US) 2015-05-06 EP disclosed
US-8957023-B2 Methods for making proteins containing free cysteine residues BOLDER BIOTECHNOLOGY INC. (US) 2015-02-17 US disclosed
US-8932828-B2 Method for preparing recombinant granulocyte colony stimulating factor cysteine muteins BOLDER BIOTECHNOLOGY, INC. (US) 2015-01-13 US disclosed
US-20130217629-A1 METHODS FOR MAKING PROTEINS CONTAINING FREE CYSTEINE RESIDUES BOLDER BIOTECHNOLOGY, INC. (US) 2013-08-22 US disclosed
US-8288126-B2 Methods for making proteins containing free cysteine residues BOLDER BIOTECHNOLOGY, INC. (US) 2012-10-16 US disclosed
US-20120064573-A1 METHODS FOR MAKING PROTEINS CONTAINING FREE CYSTEINE RESIDUES NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT 2012-03-15 US disclosed
US-20050026834-A1 Methods for making proteins containing free cysteine residues BOLDER BIOTECHNOLOGY, INC. 2005-02-03 US disclosed
US-6753165-B1 FOR RESIDUES THAT DO NOT FORM DISULFIDE BOND BOLDER BIOTECHNOLOGY, INC. 2004-06-22 US disclosed
US-20040018586-A1 Lysis, denaturing, reducing Growth hormones NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT 2004-01-29 US disclosed
EP-1284987-A2 METHODS FOR REFOLDING PROTEINS CONTAINING FREE CYSTEINE RESIDUES Bolder Biotechnology, Inc. (US) 2003-02-26 EP disclosed
EP-1144613-A4 METHODS FOR MAKING PROTEINS CONTAINING FREE CYSTEINE RESIDUES BOLDER BIOTECHNOLOGY INC (US) 2002-10-29 EP disclosed
WO-2001087925-A2 METHODS FOR REFOLDING PROTEINS CONTAINING FREE CYSTEINE RESIDUES BOLDER BIOTECHNOLOGY, INC. (US) 2001-11-22 WO disclosed
EP-1144613-A1 METHODS FOR MAKING PROTEINS CONTAINING FREE CYSTEINE RESIDUES Bolder Biotechnology, Inc. (US) 2001-10-17 EP disclosed
WO-2000042175-A1 METHODS FOR MAKING PROTEINS CONTAINING FREE CYSTEINE RESIDUES BOLDER BIOTECHNOLOGY INC. (US) 2000-07-20 WO disclosed
US-4789475-A BATHING ACTIVATED CHARCOAL IN POLYMER SOLUTION CONTAINING CHELATING AGENT, ACIDIFY ENVIRONMENTAL CONCERNS, INC. (US) 1988-12-06 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 (1 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-20070010689-A1 Optically active 3,3'-dithiobis(2-amino-2methylpropionic acid) derivative and process for producing optically active 2-amino-3-mercapto-2-methylpropionic acid derivative MPST, TPMT, ALAD NOS2 1867/4885NOS1 2455/4885NOS3 867/4885

“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.