SCHEMBL4669530

SCHEMBL4669530

Cc1ccc(S(=O)(=O)N2CCC2C(=O)O)cc1

nearest known ligand 0.62

Predicted protein targets (top 13)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 4/20 0.62
HTT P42858 1/20 0.62
MMP2 P08253 1/20 0.56
GAA P10253 1/20 0.55
HPGD P15428 1/20 0.55
POLB P06746 2/20 0.55
KMT2A Q03164 2/20 0.54
NPSR1 Q6W5P4 1/20 0.54
LMNA P02545 1/20 0.53
MAPK1 P28482 2/20 0.52
L3MBTL1 Q9Y468 1/20 0.52
FKBP1A P62942 1/20 0.51
TSHR P16473 2/20 0.50

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
SCHEMBL5702221 1.00 ALDH1A1 (0.62) ALDH1A1HTTMMP2GAAHPGD
SCHEMBL5702094 1.00 ALDH1A1 (0.62) ALDH1A1HTTMMP2GAAHPGD
SCHEMBL696506 0.92 ALDH1A1 (0.68) ALDH1A1HTTGAAHPGDPOLB
SCHEMBL2636629 0.92 ALDH1A1 (0.68) ALDH1A1HTTGAAHPGDPOLB
SCHEMBL696505 0.92 ALDH1A1 (0.68) ALDH1A1HTTGAAHPGDPOLB
Hydrochloric Acid SCHEMBL4077466 0.91 ALDH1A1 (0.67) ALDH1A1HTTGAAHPGDPOLB
Hydrochloric Acid SCHEMBL4077465 0.91 ALDH1A1 (0.67) ALDH1A1HTTGAAHPGDPOLB
Water SCHEMBL5497101 0.91 ALDH1A1 (0.67) ALDH1A1HTTGAAHPGDPOLB
SCHEMBL6302459 0.88 ALDH1A1 (0.64) ALDH1A1HTTGAAHPGDPOLB
SCHEMBL16635434 0.86 ALDH1A1 (0.59) ALDH1A1HTTGAALMNAL3MBTL1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1193253-B1 PROCESS FOR PRODUCING OPTICALLY ACTIVE AZETIDINE-2-CARBOXYLIC ACIDS KANEKA CORP (JP) 2008-06-25 EP disclosed
EP-1927588-A2 Process for producing optically active azetidine-2-carboxylic acids KANEKA CORPORATION (JP) 2008-06-04 EP disclosed
US-7262308-B2 Process for producing optically active azetidine-2-carboxylic acids KANEKA CORPORATION (JP) 2007-08-28 US disclosed
EP-0974670-B1 Process for producing optically active N-substituted azetidine-2-carboxylic acid compound SUMITOMO CHEMICAL CO (JP) 2006-09-13 EP disclosed
US-20050043547-A1 Process for producing optically active azetidine-2-carboxylic acids HONDA TATSUYA (JP) 2005-02-24 US disclosed
US-6838567-B1 Process for producing optically active azetidine-2-carboxylic acids KANEKA CORPORATION (JP) 2005-01-04 US disclosed
US-20040171849-A1 Process for producing optically active azetidine-2-carboxylic acid KANEKA CORPORATION (JP) 2004-09-02 US disclosed
EP-1415985-A1 PROCESS FOR PRODUCING OPTICALLY ACTIVE AZETIDINE-2-CARBOXYLIC ACID KANEKA CORPORATION (JP) 2004-05-06 EP disclosed
CN-1125064-C 3-pyridyl enantiomers and their use as analgesics ABBOTT LAB (US) 2003-10-22 CN disclosed
EP-0992491-B1 PROCESSES FOR PRODUCING AZETIDINE-2-CARBOXYLIC ACID AND INTERMEDIATES THEREOF KANEKA CORP (JP) 2003-03-05 EP disclosed
EP-1047690-A1 HETEROCYCLIC ETHER AND THIOETHER COMPOUNDS USEFUL IN CONTROLLING CHEMICAL SYNAPTIC TRANSMISSION Abbott Laboratories (US) 2000-11-02 EP disclosed
US-6133253-A NEURONAL CELL DEATH PREVENTORS AND ANTI-INFLAMMATORIES ABBOTT LABORATORIES (US) 2000-10-17 US disclosed
EP-0992491-A1 PROCESSES FOR PRODUCING AZETIDINE-2-CARBOXYLIC ACID AND INTERMEDIATES THEREOF KANEKA CORPORATION (JP) 2000-04-12 EP disclosed
CN-1245496-A 3-pyridyl enantiomers and their use as analgesics ABBOTT LAB (US) 2000-02-23 CN disclosed
EP-0974670-A2 Process for producing optically active N-substituted azetidine-2-carboxylic acid compound SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2000-01-26 EP disclosed
EP-0950057-A1 3-PYRIDYL ENANTIOMERS AND THEIR USE AS ANALGESICS Abbott Laboratories (US) 1999-10-20 EP disclosed
US-5948793-A 3-pyridyloxymethyl heterocyclic ether compounds useful in controlling neurotransmitter release ABBOTT LABORATORIES (US) 1999-09-07 US disclosed
WO-1999032480-A1 HETEROCYCLIC ETHER AND THIOETHER COMPOUNDS USEFUL IN CONTROLLING CHEMICAL SYNAPTIC TRANSMISSION ABBOTT LABORATORIES (US) 1999-07-01 WO disclosed
US-5914328-A CONTROL DOPAMINE RELEASE, ACTIVATE CHOLINERGIC CHANNELS ABBOTT LABORATORIES (US) 1999-06-22 US disclosed
WO-1998025920-A1 3-PYRIDYL ENANTIOMERS AND THEIR USE AS ANALGESICS ABBOTT LABORATORIES (US) 1998-06-18 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 (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-20040171849-A1 Process for producing optically active azetidine-2-carboxylic acid HBB, ADCY2, ADCY9 ALDH1A1 587/4885HTT 949/4885MMP2 1999/4885
US-20050043547-A1 Process for producing optically active azetidine-2-carboxylic acids AZI2, ALAD, HBB ALDH1A1 1133/4885HTT 644/4885MMP2 3417/4885

“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.