SCHEMBL1627274

SCHEMBL1627274

N[C@@H](Cc1nc2ccccc2o1)C(=O)O

nearest known ligand 0.53

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
NPC1 O15118 3/20 0.53
RAB9A P51151 3/20 0.53
MAPT P10636 2/20 0.53
LOXL2 Q9Y4K0 1/20 0.51
TP53 P04637 2/20 0.49
SMN1; SMN2 Q16637 2/20 0.49
LMNA P02545 1/20 0.49
ALPI P09923 1/20 0.49
PKM P14618 1/20 0.49
PTGS1 P23219 1/20 0.49
XIAP P98170 1/20 0.49
SLC7A5 Q01650 1/20 0.49
HTT P42858 1/20 0.46
GFER P55789 1/20 0.46
PTPRA P18433 1/20 0.46
PTPRB P23467 1/20 0.46
MEN1 O00255 2/20 0.44
KMT2A Q03164 2/20 0.44
DRD2 P14416 1/20 0.43
DRD4 P21917 1/20 0.43

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
SCHEMBL5288034 1.00 NPC1 (0.53) NPC1RAB9AMAPTLOXL2TP53
SCHEMBL11099516 1.00 NPC1 (0.53) NPC1RAB9AMAPTLOXL2TP53
SCHEMBL7909117 0.86 NPC1 (0.58) NPC1RAB9AMAPTLOXL2TP53
SCHEMBL11096618 0.84 AKR1B1 (0.46) ALPIPKMPTGS1XIAPSLC7A5
SCHEMBL4484665 0.83 RAB9A (0.54) NPC1RAB9AMAPTLOXL2TP53
SCHEMBL6505533 0.83 NPC1 (0.47) NPC1RAB9AMAPTLOXL2TP53
SCHEMBL8298679 0.83 NPC1 (0.47) NPC1RAB9AMAPTLOXL2TP53
SCHEMBL30714783 0.82 RAB9A (0.46) NPC1RAB9AMAPTLOXL2TP53
SCHEMBL11099435 0.80 MEN1 (0.50) MAPTSMN1; SMN2LMNAPTPRAPTPRB
SCHEMBL11100833 0.80 GAA (0.45) NPC1RAB9AMAPTTP53SMN1; SMN2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2020230780-A1 Ras INHIBITORY PEPTIDE 一丸ファルコス株式会社 2020-11-19 WO claimed
US-7927579-B2 Compounds comprising modified secondary ligand binding site for treatment and prevention of infections, diabetes, emphysema, viral, endocrine and cell proliferative disorders ADVANCED PROTEOME THERAPEUTICS, INC (US) 2011-04-19 US claimed
EP-1592801-B1 Method for identifying activated polymer complexes for secondary site-specific modification of protein target groups. ADVANCED PROTEOME THERAPEUTICS (US) 2010-05-05 EP claimed
EP-1592801-A4 TANDEM ANALYSES OF NONCOVALENTLY DRIVEN EFFECTORS FOR MODULATORY MAPPING OF ACTIVITIES OF PROTEIN SITES ADVANCED PROTEOME THERAPEUTICS (US) 2008-04-30 EP claimed
EP-1592801-A2 TANDEM ANALYSES OF NONCOVALENTLY DRIVEN EFFECTORS FOR MODULATORY MAPPING OF ACTIVITIES OF PROTEIN SITES Advanced Proteome Therapeutics Inc. (US) 2005-11-09 EP claimed
US-20040176575-A1 Tandem analyses of noncovalently driven effectors for modulatory mapping of activities of protein sites ADVANCED PROTEOME THERAPEUTICS, INC. 2004-09-09 US claimed
WO-2004066917-A2 TANDEM ANALYSES OF NONCOVALENTLY DRIVEN EFFECTORS FOR MODULATORY MAPPING OF ACTIVITIES OF PROTEIN SITES ADVANCED PROTEOME THERAPEUTICS, INC (US) 2004-08-12 WO claimed
US-11858905-B1 Cathepsin L inhibitors BIOFRONT THERAPEUTICS (BEIJING) CO., LTD. (CN) 2024-01-02 US disclosed
CN-116589425-A Cathepsin L inhibitors 百放英库医药科技(北京)有限公司 2023-08-15 CN disclosed
WO-2020230780-A1 Ras INHIBITORY PEPTIDE 一丸ファルコス株式会社 2020-11-19 WO disclosed
US-7927579-B2 Compounds comprising modified secondary ligand binding site for treatment and prevention of infections, diabetes, emphysema, viral, endocrine and cell proliferative disorders ADVANCED PROTEOME THERAPEUTICS, INC (US) 2011-04-19 US disclosed
EP-1592801-B1 Method for identifying activated polymer complexes for secondary site-specific modification of protein target groups. ADVANCED PROTEOME THERAPEUTICS (US) 2010-05-05 EP disclosed
EP-1592801-A4 TANDEM ANALYSES OF NONCOVALENTLY DRIVEN EFFECTORS FOR MODULATORY MAPPING OF ACTIVITIES OF PROTEIN SITES ADVANCED PROTEOME THERAPEUTICS (US) 2008-04-30 EP disclosed
EP-1592801-A2 TANDEM ANALYSES OF NONCOVALENTLY DRIVEN EFFECTORS FOR MODULATORY MAPPING OF ACTIVITIES OF PROTEIN SITES Advanced Proteome Therapeutics Inc. (US) 2005-11-09 EP disclosed
US-20040176575-A1 Tandem analyses of noncovalently driven effectors for modulatory mapping of activities of protein sites ADVANCED PROTEOME THERAPEUTICS, INC. 2004-09-09 US disclosed
WO-2004066917-A2 TANDEM ANALYSES OF NONCOVALENTLY DRIVEN EFFECTORS FOR MODULATORY MAPPING OF ACTIVITIES OF PROTEIN SITES ADVANCED PROTEOME THERAPEUTICS, INC (US) 2004-08-12 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-11858905-B1 Cathepsin L inhibitors CTSV, CTSL, CTSB NPC1 84/4885RAB9A 826/4885MAPT 1443/4885
US-20040176575-A1 Tandem analyses of noncovalently driven effectors for modulatory mapping of activities of protein sites CHAMP1, STUB1, PTMS NPC1 4360/4885RAB9A 2808/4885MAPT 3821/4885

“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.