SCHEMBL528445

SCHEMBL528445

CCc1ccccc1NC(=O)c1ccccc1

nearest known ligand 0.77

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
KCNK3 O14649 1/20 0.77
KCNK9 Q9NPC2 1/20 0.77
MAPT P10636 4/20 0.66
HPGD P15428 2/20 0.66
LMNA P02545 2/20 0.66
CYP1A2 P05177 1/20 0.66
CYP3A4 P08684 1/20 0.66
CYP2C19 P33261 1/20 0.66
POLB P06746 1/20 0.62
ALDH1A1 P00352 1/20 0.59
NR1H4 Q96RI1 1/20 0.59
HTT P42858 1/20 0.59
NPSR1 Q6W5P4 1/20 0.59
L3MBTL1 Q9Y468 1/20 0.59
KMT2A Q03164 2/20 0.58
TP53 P04637 2/20 0.58
MDM4 O15151 1/20 0.58
HDAC3 O15379 1/20 0.58
MAPK1 P28482 1/20 0.58
HDAC1 Q13547 1/20 0.58

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
SCHEMBL27616908 0.92 KCNK3 (0.68) KCNK3KCNK9MAPTHPGDLMNA
SCHEMBL2914620 0.89 KCNK3 (0.68) KCNK3KCNK9MAPTHPGDLMNA
SCHEMBL2309216 0.86 MAPT (0.63) KCNK3KCNK9MAPTHPGDLMNA
SCHEMBL7291079 0.85 NR1H4 (0.76) KCNK3KCNK9MAPTHPGDLMNA
SCHEMBL16532204 0.85 SLC16A3 (0.61) KCNK3KCNK9MAPTHPGDLMNA
SCHEMBL14492571 0.85 KCNK3 (0.63) KCNK3KCNK9MAPTHPGDLMNA
SCHEMBL948318 0.84 MAPT (0.59) KCNK3KCNK9MAPTHPGDLMNA
SCHEMBL11171600 0.84 EPHX1 (0.68) KCNK3KCNK9MAPTHPGDLMNA
SCHEMBL6971074 0.84 NR1H4 (0.57) KCNK3KCNK9MAPTHPGDLMNA
SCHEMBL21711305 0.84 NR1H4 (0.75) KCNK3KCNK9HPGDCYP1A2CYP3A4

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 18 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-109438348-A The preparation method and preparation method thereof of one kind (S) -1- phenyl -1,2,3,4- tetrahydroisoquinoline 凯瑞斯德生化(苏州)有限公司 2019-03-08 CN claimed
WO-2012014127-A1 5-LIPOXYGENASE INHIBITORS RANBAXY LABORATORIES LIMITED (IN) 2012-02-02 WO claimed
CN-1155278-A Arylthio compounds as antibacteral and antiviral agents WARNER LAMBERT CO (US) 1997-07-23 CN claimed
CN-212283980-U (S) -1-phenyl-1, 2,3, 4-tetrahydroisoquinoline synthesis reaction kettle 济南爱思医药科技有限公司 2021-01-05 CN disclosed
CN-211837857-U Synthetic suction filter device of solifenacin intermediate component 济南爱思医药科技有限公司 2020-11-03 CN disclosed
CN-110218158-A A method of photocatalytic synthesis is at amide compound in water phase 福建医科大学 2019-09-10 CN disclosed
CN-109438348-A The preparation method and preparation method thereof of one kind (S) -1- phenyl -1,2,3,4- tetrahydroisoquinoline 凯瑞斯德生化(苏州)有限公司 2019-03-08 CN disclosed
CN-109438348-A The preparation method and preparation method thereof of one kind (S) -1- phenyl -1,2,3,4- tetrahydroisoquinoline 凯瑞斯德生化(苏州)有限公司 2019-03-08 CN disclosed
EP-3008045-B1 ANTIBACTERIAL THIAZOLECARBOXYLIC ACIDS ANTABIO SAS (FR) 2018-05-09 EP disclosed
US-20170166560-A1 FIVE-MEMBERED HETEROCYCLES USEFUL AS SERINE PROTEASE INHIBITORS BRISTOL MYERS SQUIBB CO (US) 2017-06-15 US disclosed
US-9617224-B2 Five-membered heterocycles useful as serine protease inhibitors BRISTOL-MYERS SQUIBB COMPANY (US) 2017-04-11 US disclosed
CN-106279013-A A kind of method directly being catalyzed and synthesized amide by carboxylic acid and amine 中国石油大学(北京) 2017-01-04 CN disclosed
WO-2016008862-A1 SUBSTITUTED VINYL AND ALKYNYL CYANOCYCLOALKANOLS AND VINYL AND ALKYNYL CYANOHETEROCYCLOALKANOLS AS ACTIVE AGENTS AGAINST ABIOTIC PLANT STRESS BAYER CROPSCIENCE AKTIENGESELLSCHAFT (DE) 2016-01-21 WO disclosed
US-20150259297-A1 FIVE-MEMBERED HETEROCYCLES USEFUL AS SERINE PROTEASE INHIBITORS BRISTOL MYERS SQUIBB CO (US) 2015-09-17 US disclosed
US-9079860-B2 Five-membered heterocycles useful as serine protease inhibitors BRISTOL-MYERS SQUIBB COMPANY (US) 2015-07-14 US disclosed
US-8716492-B2 Five-membered heterocycles useful as serine protease inhibitors BRISTOL-MYERS SQUIBB COMPANY (US) 2014-05-06 US disclosed
CN-103159677-A 1-phenyl-1, 2, 3, 4-tetrahydroisoquinoline preparation method JINAN SHENGQUAN HEALTANG BIOLOG TECHNOLOGY CO LTD 2013-06-19 CN disclosed
WO-2012139891-A1 SUBSTITUTED VINYL AND ALKINYL CYCLOHEXENOLS AS ACTIVE AGENTS AGAINST ABIOTIC STRESS IN PLANTS BAYER CROPSCIENCE AG (DE) 2012-10-18 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-20170166560-A1 FIVE-MEMBERED HETEROCYCLES USEFUL AS SERINE PROTEASE INHIBITORS F12, F11, F5 KCNK3 342/4885KCNK9 352/4885MAPT 4157/4885
US-20150259297-A1 FIVE-MEMBERED HETEROCYCLES USEFUL AS SERINE PROTEASE INHIBITORS F12, F11, F5 KCNK3 342/4885KCNK9 352/4885MAPT 4157/4885

“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.