SCHEMBL42364

SCHEMBL42364

O=C(O)c1[nH]c2ccc(Cl)cc2c1-c1ccccc1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
MAP2 P11137 4/20 1.00
ALDH1A1 P00352 5/20 0.73
KDM4E B2RXH2 5/20 0.73
HPGD P15428 3/20 0.69
MEN1 O00255 2/20 0.69
KMT2A Q03164 2/20 0.69
HTT P42858 1/20 0.69
GFER P55789 1/20 0.69
HSD17B10 Q99714 1/20 0.69
MAPT P10636 4/20 0.68
POLB P06746 1/20 0.68
CYP1A2 P05177 1/20 0.68
XBP1 P17861 1/20 0.68
CYP2C19 P33261 1/20 0.68
GPR35 Q9HC97 3/20 0.64
ATM Q13315 1/20 0.64
GAA P10253 1/20 0.61
NPSR1 Q6W5P4 1/20 0.61
ROCK2 O75116 1/20 0.59
MAP4K4 O95819 1/20 0.59

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
SCHEMBL2716626 0.90 MAP2 (0.81) MAP2ALDH1A1KDM4EHPGDMEN1
SCHEMBL11403058 0.88 MAP2 (1.00) MAP2ALDH1A1KDM4EHPGDMAPT
SCHEMBL8686991 0.88 MAP2 (1.00) MAP2ALDH1A1KDM4EHPGDMEN1
SCHEMBL8938266 0.85 MAP2 (0.74) MAP2ALDH1A1KDM4EHPGDMEN1
SCHEMBL20570856 0.84 MAP2 (0.73) MAP2ALDH1A1KDM4EHPGDMEN1
SCHEMBL4847744 0.84 MAP2 (0.72) MAP2ALDH1A1KDM4EMEN1KMT2A
SCHEMBL27444635 0.84 MAP2 (0.71) MAP2ALDH1A1KDM4EHPGDMEN1
SCHEMBL9816507 0.83 KDM4E (0.79) MAP2ALDH1A1KDM4EHPGDMEN1
Hydrochloric Acid SCHEMBL4854389 0.83 MAP2 (0.71) MAP2ALDH1A1KDM4EMEN1KMT2A
SCHEMBL39977 0.83 MAP2 (0.71) MAP2ALDH1A1KDM4EHPGDMEN1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20030105140-A1 Substituted indole-2-carboxylic acid benzylidene-hydrazides and analogs as activators of caspases and inducers of apoptosis and the use thereof CYTOVIA, INC. 2003-06-05 US claimed
WO-2002102301-A2 SUBSTITUTED INDOLE-2-CARBOXYLIC ACID BENZYLIDENE-HYDRAZIDES AND ANALOGS AS ACTIVATORS OF CASPASES AND INDUCERS OF APOPTOSIS AND THE USE THEREOF CYTOVIA, INC. (US) 2002-12-27 WO claimed
US-20020128292-A1 Substituted indole-2-carboxylic acid benzylidene-hydrazides and analogs as activators of caspases and inducers of apoptosis and the use thereof CYTOVIA, INC. 2002-09-12 US claimed
EP-1237849-A1 ACTIVATORS OF SOLUBLE GUANYLATE CYCLASE UNIVERSITY COLLEGE LONDON (GB) 2002-09-11 EP claimed
WO-2001032604-A1 ACTIVATORS OF SOLUBLE GUANYLATE CYCLASE UNIVERSITY COLLEGE LONDON (GB) 2001-05-10 WO claimed
CN-117800969-B Tumor necrosis factor receptor complex inhibitors and uses thereof 武汉厚先生物医药有限公司 2024-11-29 CN disclosed
CN-117800969-A Tumor necrosis factor receptor complex inhibitors and uses thereof 武汉厚先生物医药有限公司 2024-04-02 CN disclosed
WO-2023275357-A1 CASPASE-2 INHIBITOR COMPOUNDS Kintsugi Therapeutics S.L. (ES) 2023-01-05 WO disclosed
EP-4112631-A1 CASPASE-2 INHIBITOR COMPOUNDS Kintsugi Therapeutics S.L. (ES) 2023-01-04 EP disclosed
US-10859585-B2 Lipid probes and uses thereof THE SCRIPPS RESEARCH INSTITUTE (US) 2020-12-08 US disclosed
US-20190293666-A1 LIPID PROBES AND USES THEREOF SCRIPPS RESEARCH INST (US) 2019-09-26 US disclosed
US-10168342-B2 Lipid probes and uses thereof THE SCRIPPS RESEARCH INSTITUTE (US) 2019-01-01 US disclosed
US-6747052-B2 ANTICANCER AGENTS CYTOVIA, INC. 2004-06-08 US disclosed
CN-1491207-A Acylated indanyl amines and their use as pharmaceuticals ������ҽҩ�¹����޹�˾ 2004-04-21 CN disclosed
US-20030105140-A1 Substituted indole-2-carboxylic acid benzylidene-hydrazides and analogs as activators of caspases and inducers of apoptosis and the use thereof CYTOVIA, INC. 2003-06-05 US disclosed
WO-2002102301-A2 SUBSTITUTED INDOLE-2-CARBOXYLIC ACID BENZYLIDENE-HYDRAZIDES AND ANALOGS AS ACTIVATORS OF CASPASES AND INDUCERS OF APOPTOSIS AND THE USE THEREOF CYTOVIA, INC. (US) 2002-12-27 WO disclosed
US-20020128292-A1 Substituted indole-2-carboxylic acid benzylidene-hydrazides and analogs as activators of caspases and inducers of apoptosis and the use thereof CYTOVIA, INC. 2002-09-12 US disclosed
EP-1237849-A1 ACTIVATORS OF SOLUBLE GUANYLATE CYCLASE UNIVERSITY COLLEGE LONDON (GB) 2002-09-11 EP disclosed
WO-2001032604-A1 ACTIVATORS OF SOLUBLE GUANYLATE CYCLASE UNIVERSITY COLLEGE LONDON (GB) 2001-05-10 WO disclosed
US-4263304-A 7 H-indolo[2,3-c]isoquinolines SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 1981-04-21 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 (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-20020128292-A1 Substituted indole-2-carboxylic acid benzylidene-hydrazides and analogs as activators of caspases and inducers of apoptosis and the use thereof BAD, API5, CASP2 MAP2 722/4885ALDH1A1 144/4885KDM4E 2887/4885
US-20030105140-A1 Substituted indole-2-carboxylic acid benzylidene-hydrazides and analogs as activators of caspases and inducers of apoptosis and the use thereof BAD, API5, CASP2 MAP2 722/4885ALDH1A1 144/4885KDM4E 2887/4885

“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.