SCHEMBL6842346

SCHEMBL6842346

Cc1c(C(=O)NN=Cc2ccccc2)[nH]c2ccc(Cl)cc12

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
MAPT P10636 6/20 1.00
LMNA P02545 5/20 1.00
SMN1; SMN2 Q16637 3/20 1.00
THRB P10828 2/20 1.00
MEN1 O00255 6/20 0.87
KMT2A Q03164 6/20 0.87
ALDH1A1 P00352 4/20 0.77
KDM4E B2RXH2 3/20 0.77
TUBB4A P04350 2/20 0.62
TUBB P07437 2/20 0.62
TUBA3C P0DPH7 2/20 0.62
TUBA1B P68363 2/20 0.62
TUBA4A P68366 2/20 0.62
TUBB4B P68371 2/20 0.62
TUBB3 Q13509 2/20 0.62
TUBB2A Q13885 2/20 0.62
TUBB8 Q3ZCM7 2/20 0.62
TUBA3E Q6PEY2 2/20 0.62
TUBA1A Q71U36 2/20 0.62
TUBA1C Q9BQE3 2/20 0.62

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
SCHEMBL7557760 0.86 MAPT (0.74) MAPTLMNASMN1; SMN2THRBMEN1
SCHEMBL7557764 0.86 MAPT (0.74) MAPTLMNASMN1; SMN2THRBMEN1
SCHEMBL7532157 0.84 MAPT (0.83) MAPTLMNASMN1; SMN2THRBMEN1
SCHEMBL7566603 0.84 MAPT (0.83) MAPTLMNASMN1; SMN2THRBMEN1
SCHEMBL7673063 0.78 MAPT (0.70) MAPTLMNASMN1; SMN2THRBMEN1
SCHEMBL7527624 0.78 MAPT (0.70) MAPTLMNASMN1; SMN2THRBMEN1
SCHEMBL7562862 0.78 MAPT (0.64) MAPTLMNASMN1; SMN2THRBMEN1
SCHEMBL7562857 0.78 MAPT (0.64) MAPTLMNASMN1; SMN2THRBMEN1
SCHEMBL7560117 0.78 MAPT (0.64) MAPTLMNASMN1; SMN2THRBMEN1
SCHEMBL7560111 0.78 MAPT (0.64) MAPTLMNASMN1; SMN2THRBMEN1

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 7 patents. 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
US-6747052-B2 ANTICANCER AGENTS CYTOVIA, INC. 2004-06-08 US 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

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 MAPT 4140/4885LMNA 1924/4885SMN1; SMN2 4410/4885
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 MAPT 4140/4885LMNA 1924/4885SMN1; SMN2 4410/4885

“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.