SCHEMBL2904552

SCHEMBL2904552

O=C(O)C(O)(C(=O)c1ccccc1)[C@@](O)(C(=O)O)C(=O)c1ccccc1

nearest known ligand 0.58

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CES1 P23141 7/20 0.58
SRC P12931 1/20 0.52
CES2 O00748 4/20 0.50
TSHR P16473 2/20 0.50
ALDH1A1 P00352 2/20 0.50
DAO P14920 1/20 0.50
NAPRT Q6XQN6 1/20 0.50
TDP1 Q9NUW8 4/20 0.46
MAPT P10636 3/20 0.46
CYP3A4 P08684 2/20 0.46
CA2 P00918 2/20 0.46
CA4 P22748 2/20 0.46
HSD17B10 Q99714 2/20 0.46
L3MBTL1 Q9Y468 2/20 0.46
CA12 O43570 2/20 0.46
CA1 P00915 2/20 0.46
CA9 Q16790 2/20 0.46
POLB P06746 1/20 0.46
PARP1 P09874 1/20 0.46
CYP2C19 P33261 1/20 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
SCHEMBL414466 1.00 CES1 (0.58) CES1SRCCES2TSHRALDH1A1
SCHEMBL31097912 1.00 CES1 (0.58) CES1SRCCES2TSHRALDH1A1
SCHEMBL32681153 1.00 CES1 (0.58) CES1SRCCES2TSHRALDH1A1
SCHEMBL7684 1.00 CES1 (0.58) CES1SRCCES2TSHRALDH1A1
SCHEMBL637241 1.00 CES1 (0.58) CES1SRCCES2TSHRALDH1A1
SCHEMBL11542843 0.97 CES1 (0.56) CES1SRCCES2TSHRALDH1A1
Water SCHEMBL18124365 0.97 CES1 (0.56) CES1SRCCES2TSHRALDH1A1
Water SCHEMBL19283519 0.97 CES1 (0.56) CES1SRCCES2TSHRALDH1A1
Ammonia Solution, Strong SCHEMBL11444696 0.97 CES1 (0.56) CES1SRCCES2TSHRALDH1A1
Ammonia Solution, Strong SCHEMBL11444694 0.97 CES1 (0.56) CES1SRCCES2TSHRALDH1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-103140486-B Co-crystals and salts of CCR 3-inhibitors 贝林格尔.英格海姆国际有限公司 2016-08-03 CN claimed
CN-101111478-B Optical resolution method of amlodipine SK CHEMICALS CO LTD 2012-04-04 CN claimed
CN-101111478-A Optical resolution method of amlodipine SK CHEMICALS CO LTD (KR) 2008-01-23 CN claimed
US-9408852-B2 Method of lowering serum uric acid levels with (S)-tofisopam PHARMOS CORPORATION (US) 2016-08-09 US disclosed
CN-103140486-B Co-crystals and salts of CCR 3-inhibitors 贝林格尔.英格海姆国际有限公司 2016-08-03 CN disclosed
CN-103140486-A Co-crystals and salts of CCR 3-inhibitors BOEHRINGER INGELHEIM INT 2013-06-05 CN disclosed
US-20130045966-A1 Method of Lowering Serum Uric Acid Levels With (S)-Tofisopam PHARMOS CORPORATION (US) 2013-02-21 US disclosed
EP-1594509-B1 COMPOSITIONS AND METHODS FOR TREATMENT OF IRRITABLE BOWEL SYNDROME AND NONULCER DYSPEPSIA VELA ACQUISITION CORP (US) 2010-08-11 EP disclosed
US-7745431-B2 Pharmaceutical composition of 1-(3,4-dimethoxyphenyl)-4-methyl-5-ethyl-7-methoxy-8-hydroxy-5H-2,3-benzodiazepine and uses thereof VELA ACQUISITION CORPORATION (US) 2010-06-29 US disclosed
EP-1755614-A4 COMPOSITIONS AND METHODS FOR TREATMENT OF NEUROPATHIC PAIN, FIBROMYALGIA AND CHRONIC FATIGUE SYNDROME VELA PHARMACEUTICALS INC (US) 2009-06-10 EP disclosed
EP-1594509-A4 COMPOSITIONS AND METHODS FOR TREATMENT OF IRRITABLE BOWEL SYNDROME AND NONULCER DYSPEPSIA VELA ACQUISITION CORP (US) 2009-06-03 EP disclosed
US-20040157833-A1 Pharmaceutical composition of 1- (3,4-dimethoxyphenyl)-4-methyl-5-ethyl-7-methoxy-8-hydroxy-5H-2,3-benzodiazepine and uses thereof VELA PHARMACEUTICALS, INC. 2004-08-12 US disclosed
US-20040152695-A1 Pharmaceutical composition of 1-(3-hydroxy-4-methoxyphenyl)-4-methyl-5-ethyl-7,8-dimethoxy-5H-2,3-benzodiazepine and uses thereof VELA PHARMACEUTICALS, INC. 2004-08-05 US disclosed
US-20040138210-A1 Method of increasing neutrophil production using 2,3-benzodiazepines VELA PHARMACEUTICALS, INC. 2004-07-15 US disclosed
US-20040138209-A1 Treatment of inflammatory disorders with 2,3- benzodiazepines VELA PHARMACEUTICALS, INC. 2004-07-15 US disclosed
WO-2004050615-A2 METHOD OF INCREASING NEUTROPHIL PRODUCTION USING 2,3-BENZODIAZEPINES VELA PHARMACEUTICALS, INC. (US) 2004-06-17 WO disclosed
WO-2004050040-A2 PHARMACEUTICAL COMPOSITION OF 1-(3,4-DIMETHOXYPHENYL)-4-METHYL-5-ETHYL-7-METHOXY-8-HYDROXY-5H-2,3-BENZODIAZEPINE AND USES THEREOF VELA PHARMACEUTICALS, INC. (US) 2004-06-17 WO disclosed
US-20040106602-A1 Treatment of LTB4-mediated inflammatory disorders with optically-pure (R)-2,3-benzodiazepines VELA ACQUISITION CORPORATION 2004-06-03 US disclosed
US-20040106601-A1 Method of increasing neutrophil production using optically-pure (R)-2,3-benzodiazepines VELA ACQUISITION CORPORATION 2004-06-03 US disclosed
US-6683072-B1 EFFECTIVE LONG TERM ALLEVIATION VELA PHARMACEUTICALS, INC. 2004-01-27 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 (7 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-20040138209-A1 Treatment of inflammatory disorders with 2,3- benzodiazepines LTB4R2, LTB4R, GABRA4 CES1 475/4885SRC 4785/4885CES2 848/4885
US-20040157833-A1 Pharmaceutical composition of 1- (3,4-dimethoxyphenyl)-4-methyl-5-ethyl-7-methoxy-8-hydroxy-5H-2,3-benzodiazepine and uses thereof GABRA4, GABBR1, GABRB2 CES1 1420/4885SRC 3184/4885CES2 1310/4885
US-20040106602-A1 Treatment of LTB4-mediated inflammatory disorders with optically-pure (R)-2,3-benzodiazepines LTB4R2, LTB4R, PTGER4 CES1 586/4885SRC 4724/4885CES2 1486/4885
US-20040152695-A1 Pharmaceutical composition of 1-(3-hydroxy-4-methoxyphenyl)-4-methyl-5-ethyl-7,8-dimethoxy-5H-2,3-benzodiazepine and uses thereof GABRA4, GABRA2, GABRB2 CES1 1410/4885SRC 2649/4885CES2 1548/4885
US-20040106601-A1 Method of increasing neutrophil production using optically-pure (R)-2,3-benzodiazepines OPRL1, OPRD1, GABRR1 CES1 342/4885SRC 4410/4885CES2 153/4885
US-20040138210-A1 Method of increasing neutrophil production using 2,3-benzodiazepines GABRR1, GABRA1, GABRA3 CES1 538/4885SRC 4806/4885CES2 210/4885
US-20130045966-A1 Method of Lowering Serum Uric Acid Levels With (S)-Tofisopam ATIC, NPPA, XPNPEP1 CES1 368/4885SRC 4626/4885CES2 1865/4885

“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.