SCHEMBL661545

SCHEMBL661545

Cc1cccc(C(=O)NN)c1

nearest known ligand 0.69

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
HDAC8 Q9BY41 1/20 0.69
HDAC6 Q9UBN7 1/20 0.69
SMN1; SMN2 Q16637 2/20 0.65
KDM4E B2RXH2 1/20 0.63
ALDH1A1 P00352 1/20 0.63
MEN1 O00255 3/20 0.62
KMT2A Q03164 3/20 0.62
KCNK3 O14649 2/20 0.62
KCNK9 Q9NPC2 2/20 0.62
KCNH2 Q12809 1/20 0.62
PARP1 P09874 1/20 0.62
RAB9A P51151 3/20 0.59
TAS1R3 Q7RTX0 1/20 0.58
TAS1R1 Q7RTX1 1/20 0.58
RXFP1 Q9HBX9 1/20 0.58
NPC1 O15118 2/20 0.57
POLB P06746 2/20 0.57
TP53 P04637 1/20 0.57
ATM Q13315 1/20 0.57
MAPT P10636 1/20 0.56

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
Hydrochloric Acid SCHEMBL28427527 0.98 HDAC8 (0.67) HDAC8HDAC6SMN1; SMN2KDM4EALDH1A1
Acetic Acid SCHEMBL8172858 0.94 SMN1; SMN2 (0.64) HDAC8HDAC6SMN1; SMN2KDM4EALDH1A1
Benzoic Acid Hydrazide SCHEMBL11833590 0.94 SMN1; SMN2 (0.74) HDAC8HDAC6SMN1; SMN2KDM4EALDH1A1
SCHEMBL28283623 0.93 HDAC8 (0.61) HDAC8HDAC6SMN1; SMN2KDM4EALDH1A1
Water SCHEMBL8856536 0.86 SMN1; SMN2 (0.54) HDAC8HDAC6SMN1; SMN2KDM4EALDH1A1
SCHEMBL77384 0.85 ALDH1A1 (0.76) HDAC8HDAC6SMN1; SMN2KDM4EALDH1A1
SCHEMBL24931248 0.83 SMN1; SMN2 (0.89) HDAC8HDAC6SMN1; SMN2ALDH1A1MEN1
Benzoic Acid Hydrazide SCHEMBL8180423 0.82 SMN1; SMN2 (0.58) HDAC8HDAC6SMN1; SMN2KDM4EALDH1A1
Benzoic Acid Hydrazide SCHEMBL7199126 0.82 LMNA (0.61) HDAC8HDAC6SMN1; SMN2KDM4EALDH1A1
SCHEMBL30929655 0.82 HDAC6 (1.00) HDAC8HDAC6SMN1; SMN2KDM4EMEN1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-113121426-B Synthesis method of myrtenal aldehyde group dihydrazide compounds with fungal inhibition activity 广西大学 2023-01-06 CN claimed
CN-110003160-B Osthole hydrazone/acylhydrazone/sulfonylhydrazone derivatives, and preparation method and application thereof 贵州中医药大学 2022-10-11 CN claimed
CN-114875394-A Corrosion and scale inhibition zinc series metal phosphate conversion agent and preparation method thereof 安徽未来表面技术有限公司 2022-08-09 CN claimed
CN-113121382-A Metal compound material and preparation method thereof, quantum dot light-emitting diode and light-emitting device TCL集团股份有限公司 2021-07-16 CN claimed
CN-113121426-A Synthesis method of myrtenal aldehyde group dihydrazide compounds with fungal inhibition activity 广西大学 2021-07-16 CN claimed
CN-108997142-B Method for removing residual ketone in production of fatty amine by ketone method 浙江建业化工股份有限公司 2021-01-12 CN claimed
US-7781542-B2 Curing a mixture of a polyepoxide or epoxy resin, an imidazole curing agent, and an aromatic monofunctional acid hydrazide cure accelerator; reduced gel time HEXCEL COMPOSITES, LTD. (GB) 2010-08-24 US claimed
EP-1602678-B9 Cure accelerators HEXCEL COMPOSITES LTD (GB) 2008-11-05 EP claimed
EP-1602678-B1 Cure accelerators HEXCEL COMPOSITES LTD (GB) 2008-06-11 EP claimed
EP-1392219-A4 SUBSTITUTED N'-(ARYLCARBONYL)-BENZHYDRAZIDES, N'-(ARYLCARBONYL)-BENZYLIDENE-HYDRAZIDES AND ANALOGS AS ACTIVATORS OF CASPASES AND INDUCERS OF APOTOSIS AND THE USE THEREOF CYTOVIA INC (US) 2007-01-24 EP claimed
WO-2002089745-A2 SUBSTITUTED N'-(ARYLCARBONYL)-BENZHYDRAZIDES, N'-(ARYLCARBONYL)-BENZYLIDENE-HYDRAZIDES AND ANALOGS AS ACTIVATORS OF CASPASES AND INDUCERS OF APOPTOSIS AND THE USE THEREOF CYTOVIA, INC. (US) 2002-11-14 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
WO-2002038667-A2 NATURAL RUBBER PRODUCED FROM LATEX AND COMPOSITION COMPRISING THE SAME BRIDGESTONE CORPORATION (JP) 2002-05-16 WO claimed
US-20020035195-A1 Viscosity-stabilizer-containing natural rubber latex and natural rubber and a production process thereof BRIDGESTONE CORPORATION 2002-03-21 US claimed
CN-1030911-C Dibenzoylalkylcyanohydrazines ROHM & HAAS (US) 1996-02-07 CN claimed
CN-1057452-A Dibenzoyl alkyl-alkyl cyanides ROHM & HAAS (US) 1992-01-01 CN claimed
EP-0347216-A2 Insecticidal N'-substituted-N-alkylcarbonyl-N'-acylhydrazines and N'-substituted -N-acyl-N'-alkylcarbonyl hydrazines ROHM AND HAAS COMPANY (US) 1989-12-20 EP claimed
EP-0123066-B1 REACTION OF CARBONYLHYDRAZINES AND ORGANIC PEROXIDES TO FOAM UNSATURATED POLYESTER RESINS PENNWALT CORPORATION (US) 1988-10-12 EP claimed
EP-0220364-A2 Reaction of certain hydrazide compounds with free radical initiators to produce crosslinked polymer foams PENNWALT CORPORATION (US) 1987-05-06 EP claimed
US-4607060-A FREE RADICAL CATALYSIS PENNWALT CORPORATION (US) 1986-08-19 US claimed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (1 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 HDAC8 290/4885HDAC6 171/4885SMN1; 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.