SCHEMBL7877973

SCHEMBL7877973

COC(=O)c1cc2ccc(OCc3ccccc3)cc2n1C

nearest known ligand 0.68

Predicted protein targets (top 11)

geneUniProtsupporting neighboursconfidence
SRD5A2 P31213 2/20 0.68
SRD5A1 P18405 1/20 0.55
L3MBTL1 Q9Y468 1/20 0.53
MEN1 O00255 1/20 0.53
NPC1 O15118 1/20 0.53
RAB9A P51151 1/20 0.53
KMT2A Q03164 1/20 0.53
ALOX5 P09917 1/20 0.51
MRGPRX4 Q96LA9 1/20 0.47
LTB4R Q15722 1/20 0.47
LTB4R2 Q9NPC1 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
SCHEMBL30435990 1.00 SRD5A2 (0.68) SRD5A2SRD5A1L3MBTL1MEN1NPC1
SCHEMBL4464733 0.91 SRD5A2 (0.81) SRD5A2SRD5A1L3MBTL1MEN1NPC1
SCHEMBL21122766 0.87 SRD5A2 (0.57) SRD5A2MEN1NPC1RAB9AKMT2A
SCHEMBL24093799 0.87 SRD5A2 (0.57) SRD5A2MEN1NPC1RAB9AKMT2A
SCHEMBL21122759 0.85 SRD5A2 (0.55) SRD5A2MEN1NPC1RAB9AKMT2A
SCHEMBL4470968 0.81 SRD5A2 (1.00) SRD5A2SRD5A1MEN1NPC1RAB9A
SCHEMBL8687408 0.81 SRD5A2 (0.76) SRD5A2SRD5A1L3MBTL1MEN1NPC1
SCHEMBL2272634 0.80 L3MBTL1 (0.80) L3MBTL1
SCHEMBL20605152 0.80 SRD5A2 (0.52) SRD5A2SRD5A1L3MBTL1MEN1NPC1
SCHEMBL4023414 0.80 SRD5A2 (0.78) SRD5A2SRD5A1L3MBTL1MEN1NPC1

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
US-20230374017-A1 COMPOSITIONS AND METHODS FOR ACTIVATING PYRUVATE KINASE THE REGENTS OF THE UNIVERSITY OF MICHIGAN 2023-11-23 US disclosed
US-20230374017-A1 COMPOSITIONS AND METHODS FOR ACTIVATING PYRUVATE KINASE THE REGENTS OF THE UNIVERSITY OF MICHIGAN 2023-11-23 US disclosed
US-20230374017-A1 COMPOSITIONS AND METHODS FOR ACTIVATING PYRUVATE KINASE THE REGENTS OF THE UNIVERSITY OF MICHIGAN 2023-11-23 US disclosed
US-20230233700-A1 METHODS FOR PREPARING ANTIBODY DRUG CONJUGATES GENENTECH, INC. (US) 2023-07-27 US disclosed
EP-4185293-A1 COMPOSITIONS AND METHODS FOR ACTIVATING PYRUVATE KINASE The Regents of The University of Michigan (US) 2023-05-31 EP disclosed
US-11547762-B2 Methods for preparing antibody drug conjugates GENENTECH, INC. (US) 2023-01-10 US disclosed
WO-2022020424-A1 COMPOSITIONS AND METHODS FOR ACTIVATING PYRUVATE KINASE THE REGENTS OF THE UNIVERSITY OF MICHIGAN (US) 2022-01-27 WO disclosed
US-20190201544-A1 METHODS FOR PREPARING ANTIBODY DRUG CONJUGATES GENENTECH, INC. 2019-07-04 US disclosed
WO-2018065501-A1 METHODS FOR PREPARING ANTIBODY DRUG CONJUGATES F. HOFFMANN-LA ROCHE AG (CH) 2018-04-12 WO disclosed
CN-1067988-C Indoloylguanidine derivatives SUMITOMO PHARMACEUTICS K K (JP) 2001-07-04 CN disclosed
US-6248772-B1 HYPOTENSIVE AGENTS; ANTIARRHYTHMIA AGENTS; ANTIDIABETIC AGENTS; ANTIPROLIFERATIVE AGENTS SUMITOMO PHARMACEUTICALS CO., LTD. (JP) 2001-06-19 US disclosed
US-6169107-B1 USEFUL FOR THE TREATMENT AND PREVENTION OF DISEASES CAUSED BY INCREASED SODIUM/PROTON (NA.SUP.+ /H.SUP.+) EXCHANGER ACTIVITY, FOR EXAMPLE, HYPERTENSION, ARRHYTHMIA, ANGINA PECTORIS, CARDIAC HYPERTROPHY, DIABETES MELLITUS SUMITOMO PHARMACEUTICAL CO., LTD. (JP) 2001-01-02 US disclosed
CN-1051301-C Indoloylguanidine derivatives SUMITOMO PHARMA (JP) 2000-04-12 CN disclosed
EP-0622356-B1 Indoloylguanidine derivatives as inhibitors of sodium-hydrogen exchange SUMITOMO PHARMA (JP) 1998-07-01 EP disclosed
CN-1136038-A Indoloylguanidine derivatives SUMITOMO PHARMACEUTICS K K (JP) 1996-11-20 CN disclosed
EP-0708091-A2 Indoloylguanidine derivatives SUMITOMO PHARMACEUTICALS COMPANY, LIMITED (JP) 1996-04-24 EP disclosed
CN-1106800-A Indoloylguanidine derivatives SUMITOMO PHARMA (JP) 1995-08-16 CN disclosed
EP-0622356-A1 Indoloylguanidine derivatives as inhibitors of sodium-hydrogen exchange SUMITOMO PHARMACEUTICALS COMPANY, LIMITED (JP) 1994-11-02 EP 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 (4 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-20230233700-A1 METHODS FOR PREPARING ANTIBODY DRUG CONJUGATES FCGRT, MSN, FCGR3B SRD5A2 3933/4885SRD5A1 4084/4885L3MBTL1 2941/4885
US-11547762-B2 Methods for preparing antibody drug conjugates FCGRT, MSN, FCGR3B SRD5A2 3933/4885SRD5A1 4084/4885L3MBTL1 2941/4885
US-20190201544-A1 METHODS FOR PREPARING ANTIBODY DRUG CONJUGATES FCGRT, MSN, FCGR3B SRD5A2 3933/4885SRD5A1 4084/4885L3MBTL1 2941/4885
US-20230374017-A1 COMPOSITIONS AND METHODS FOR ACTIVATING PYRUVATE KINASE PCK1, PDK2, PDK1 SRD5A2 2627/4885SRD5A1 2406/4885L3MBTL1 2243/4885

“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.