SCHEMBL2592802

SCHEMBL2592802

BrCc1ccnc2ccccc12

nearest known ligand 0.64

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
LOXL2 Q9Y4K0 1/20 0.64
NCF1 P14598 1/20 0.52
HTR1A P08908 2/20 0.50
ADRA1D P25100 2/20 0.50
ADRA1A P35348 2/20 0.50
ADRA1B P35368 2/20 0.50
CYP1A2 P05177 3/20 0.47
CYP3A4 P08684 2/20 0.47
CYP2D6 P10635 1/20 0.47
HIF1A Q16665 1/20 0.47
KDM4E B2RXH2 3/20 0.46
ALDH1A1 P00352 2/20 0.46
SMN1; SMN2 Q16637 2/20 0.46
LMNA P02545 1/20 0.46
NPSR1 Q6W5P4 1/20 0.46
MAPT P10636 3/20 0.44
FERMT2 Q96AC1 1/20 0.44
NPC1 O15118 1/20 0.41
TP53 P04637 1/20 0.41
RAB9A P51151 1/20 0.41

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
SCHEMBL30200129 1.00 LOXL2 (0.64) LOXL2NCF1HTR1AADRA1DADRA1A
Bromide SCHEMBL15618161 0.98 LOXL2 (0.62) LOXL2NCF1HTR1AADRA1DADRA1A
Hydrochloric Acid SCHEMBL8762058 0.98 LOXL2 (0.62) LOXL2NCF1HTR1AADRA1DADRA1A
Benzene SCHEMBL6631416 0.98 LOXL2 (0.62) LOXL2NCF1HTR1AADRA1DADRA1A
SCHEMBL1282250 0.85 MAPT (0.54) LOXL2NCF1HTR1AADRA1DADRA1A
SCHEMBL27751565 0.83 LOXL2 (0.60) LOXL2NCF1HTR1AADRA1DADRA1A
Hydrochloric Acid SCHEMBL16752130 0.83 MAPT (0.52) LOXL2NCF1HTR1AADRA1DADRA1A
SCHEMBL334360 0.80 LOXL2 (0.67) LOXL2NCF1HTR1AADRA1DADRA1A
SCHEMBL31599195 0.80 LOXL2 (0.67) LOXL2NCF1HTR1AADRA1DADRA1A
Bromide SCHEMBL9399386 0.78 LOXL2 (0.64) LOXL2NCF1HTR1AADRA1DADRA1A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-116396260-A Genipin ether with uric acid reducing and kidney protecting functions, and preparation method and application thereof 山东省农业科学院 2023-07-07 CN claimed
EP-2948437-B1 APPROACH FOR SYNTHESIS OF CATECHINS EPIRIUM BIO INC (US) 2021-11-03 EP claimed
CN-110003159-A Synthesize the new method of catechin 斯法尔制药私人有限公司 2019-07-12 CN claimed
EP-2668176-B1 A NOVEL PROCESS FOR SYNTHESIS OF POLYPHENOLS SPHAERA PHARMA PTE LTD (SG) 2017-05-17 EP claimed
US-9556140-B2 Approach for synthesis of catechins SPHAERA PHARMA PVT. LTD. (IN) 2017-01-31 US claimed
US-9428482-B2 Process for synthesis of polyphenols SPHAERA PHARMA PTE. LTD. (SG) 2016-08-30 US claimed
US-20150368223-A1 NOVEL APPROACH FOR SYNTHESIS OF CATECHINS EPIRIUM BIO INC. 2015-12-24 US claimed
EP-2948437-A2 NOVEL APPROACH FOR SYNTHESIS OF CATECHINS Sphaera Pharma Pvt. Ltd. (IN) 2015-12-02 EP claimed
CN-105026384-A Novel method for synthesizing catechin SPHAERA PHARMA PRIVATE LTD 2015-11-04 CN claimed
WO-2014115174-A2 NOVEL APPROACH FOR SYNTHESIS OF CATECHINS SPHAERA PHARMA PVT. LTD. (IN) 2014-07-31 WO claimed
EP-1291353-A1 6-O-substituted ketolides having antibacterial activity ABBOTT LABORATORIES (US) 2003-03-12 EP claimed
EP-1007530-A1 6-O-SUBSTITUTED ERYTHROMYCIN COMPOUNDS AND METHOD FOR MAKING SAME ABBOTT LABORATORIES (US) 2000-06-14 EP claimed
US-6028181-A 6-0-Substituted antibacterial erythromycin ketolides and methods of making ABBOTT LABORATORIES (US) 2000-02-22 US claimed
CN-1237183-A 6-0-substituted ketolides with antibacterial activity ABBOTT CO (US) 1999-12-01 CN claimed
CN-1224427-A 6-O-substituted erythromycin compounds and preparation method thereof ABBOTT LAB (US) 1999-07-28 CN claimed
EP-0929563-A1 6-O-SUBSTITUTED KETOLIDES HAVING ANTIBACTERIAL ACTIVITY Abbott Laboratories (US) 1999-07-21 EP claimed
EP-0918783-A1 6-O-SUBSTITUTED ERYTHROMYCINS AND METHOD FOR MAKING THEM ABBOTT LABORATORIES (US) 1999-06-02 EP claimed
WO-1998009978-A1 6-O-SUBSTITUTED KETOLIDES HAVING ANTIBACTERIAL ACTIVITY ABBOTT LABORATORIES (US) 1998-03-12 WO claimed
WO-1997042204-A1 6-O-SUBSTITUTED ERYTHROMYCINS AND METHOD FOR MAKING THEM ABBOTT LABORATORIES (US) 1997-11-13 WO claimed
WO-1997042206-A1 6-O-SUBSTITUTED ERYTHROMYCIN COMPOUNDS AND METHOD FOR MAKING SAME ABBOTT LABORATORIES (US) 1997-11-13 WO claimed

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-20150368223-A1 NOVEL APPROACH FOR SYNTHESIS OF CATECHINS NQO1, COMT, NNMT LOXL2 4217/4885NCF1 1807/4885HTR1A 1118/4885

“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.