SCHEMBL3242065

SCHEMBL3242065

CCC(O)(CC)c1ccc(OCc2ccccc2)c(OC)c1

nearest known ligand 0.56

Predicted protein targets (top 19)

geneUniProtsupporting neighboursconfidence
NPC1 O15118 3/20 0.56
RAB9A P51151 3/20 0.56
HPGD P15428 2/20 0.56
SMN1; SMN2 Q16637 1/20 0.56
APP P05067 5/20 0.50
MTNR1A P48039 2/20 0.48
MTNR1B P49286 2/20 0.48
CTSV O60911 1/20 0.48
CTSL P07711 1/20 0.48
BCHE P06276 1/20 0.48
MEN1 O00255 3/20 0.48
KMT2A Q03164 3/20 0.48
KDM4E B2RXH2 3/20 0.47
ALDH1A1 P00352 1/20 0.47
CYP1A2 P05177 1/20 0.47
CYP3A4 P08684 1/20 0.47
CYP2D6 P10635 1/20 0.47
CYP2C9 P11712 1/20 0.47
BLM P54132 1/20 0.47

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
SCHEMBL20059953 0.86 FFAR4 (0.53) NPC1RAB9AHPGDSMN1; SMN2CYP2C9
SCHEMBL16178212 0.83 RAB9A (0.51) NPC1RAB9AHPGDSMN1; SMN2KDM4E
SCHEMBL8253237 0.82 NPC1 (0.55) NPC1RAB9AHPGDSMN1; SMN2APP
SCHEMBL3856515 0.82 L3MBTL1 (0.46) SMN1; SMN2MEN1KMT2AKDM4ECYP1A2
SCHEMBL27910124 0.81 CCR5 (0.42) NPC1RAB9AHPGDSMN1; SMN2
SCHEMBL9366130 0.80 ALOX5 (0.42) NPC1RAB9AHPGDSMN1; SMN2APP
SCHEMBL11005933 0.80 HPGD (0.53) NPC1RAB9AHPGDSMN1; SMN2APP
SCHEMBL8320013 0.78 ESR1 (0.45) NPC1RAB9AKDM4E
SCHEMBL9434950 0.78 HTR2C (0.48) NPC1RAB9AHPGDSMN1; SMN2KMT2A
SCHEMBL9597849 0.78 ALOX5 (0.57) NPC1RAB9AHPGDSMN1; SMN2APP

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
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-1581206-A4 TREATMENT OF INFLAMMATORY DISORDERS WITH 2,3-BENZODIAZEPINES VELA ACQUISITION CORP (US) 2009-01-07 EP disclosed
EP-1567161-A4 PHARMACEUTICAL COMPOSITION OF 1-(3,4-DIMETHOXYPHENYL)-4-METHYL-5-ETHYL-7-METHOXY-8-HYDROXY-5H-2,3-BENZODIAZEPINE AND USES THEREOF VELA ACQUISITION CORP (US) 2008-09-03 EP disclosed
EP-1567162-A4 TREATMENT OF IRRITABLE BOWEL SYNDROME AND NONULCER DYSPEPSIA WITH SUBSTITUTED 2,3-BENZODIAZEPINES VELA ACQUISITION CORP (US) 2008-04-30 EP disclosed
US-20070032479-A1 Treatment of inflammatory disorders of the epithelium with low dose 2,3-benzodiazepines VELA ACQUISITION CORPORATION 2007-02-08 US disclosed
US-20070032479-A1 Treatment of inflammatory disorders of the epithelium with low dose 2,3-benzodiazepines VELA ACQUISITION CORPORATION 2007-02-08 US disclosed
EP-1689408-A1 TREATMENT OF INFLAMMATORY DISORDERS OF THE EPITHELIUM WITH LOW DOSE 2,3-BENZODIAZEPINES Vela Pharmaceuticals Inc. (US) 2006-08-16 EP disclosed
US-7022700-B2 Method of increasing neutrophil production using optically-pure (R)-2,3-benzodiazepines VELA PHARMACEUTICALS, INC. (US) 2006-04-04 US disclosed
EP-1581206-A1 TREATMENT OF INFLAMMATORY DISORDERS WITH 2,3-BENZODIAZEPINES Vela Pharmaceuticals Inc. (US) 2005-10-05 EP disclosed
EP-1567161-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) 2005-08-31 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-20040138209-A1 Treatment of inflammatory disorders with 2,3- benzodiazepines VELA PHARMACEUTICALS, INC. 2004-07-15 US disclosed
US-20040138210-A1 Method of increasing neutrophil production using 2,3-benzodiazepines VELA PHARMACEUTICALS, INC. 2004-07-15 US 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
WO-2004050080-A1 TREATMENT OF INFLAMMATORY DISORDERS WITH 2,3-BENZODIAZEPINES VELA PHARMACEUTICALS, INC. (US) 2004-06-17 WO disclosed
WO-2004050615-A2 METHOD OF INCREASING NEUTROPHIL PRODUCTION USING 2,3-BENZODIAZEPINES VELA PHARMACEUTICALS, INC. (US) 2004-06-17 WO disclosed
WO-2004050616-A2 TREATMENT OF IRRITABLE BOWEL SYNDROME AND NONULCER DYSPEPSIA WITH SUBSTITUTED 2,3-BENZODIAZEPINES VELA PHARMACEUTICALS, INC. (US) 2004-06-17 WO 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-20040106602-A1 Treatment of LTB4-mediated inflammatory disorders with optically-pure (R)-2,3-benzodiazepines VELA ACQUISITION CORPORATION 2004-06-03 US disclosed
US-6638928-B1 Benzodiazepines administered for irritable bowel syndrome and nonulcer dyspepsia. VELA PHARMACEUTICALS, INC. 2003-10-28 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 (6 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 NPC1 1240/4885RAB9A 3531/4885HPGD 689/4885
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 NPC1 941/4885RAB9A 2363/4885HPGD 857/4885
US-20040106602-A1 Treatment of LTB4-mediated inflammatory disorders with optically-pure (R)-2,3-benzodiazepines LTB4R2, LTB4R, PTGER4 NPC1 1480/4885RAB9A 2968/4885HPGD 548/4885
US-20040106601-A1 Method of increasing neutrophil production using optically-pure (R)-2,3-benzodiazepines OPRL1, OPRD1, GABRR1 NPC1 844/4885RAB9A 1836/4885HPGD 213/4885
US-20070032479-A1 Treatment of inflammatory disorders of the epithelium with low dose 2,3-benzodiazepines GABBR2, GABBR1, GABRB3 NPC1 1469/4885RAB9A 2984/4885HPGD 602/4885
US-20040138210-A1 Method of increasing neutrophil production using 2,3-benzodiazepines GABRR1, GABRA1, GABRA3 NPC1 904/4885RAB9A 2306/4885HPGD 338/4885

“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.