SCHEMBL1620260

SCHEMBL1620260

O=C(O)C(=O)C=Cc1ccc(Cl)cc1

nearest known ligand 0.67

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CYP1A2 P05177 1/20 0.67
MAOB P27338 5/20 0.59
HDAC2 Q92769 2/20 0.55
CYP1B1 Q16678 1/20 0.55
CXCL12 P48061 1/20 0.53
PLAAT3 P53816 1/20 0.53
PLAAT5 Q96KN8 1/20 0.53
PLAAT2 Q9NWW9 1/20 0.53
PLAAT4 Q9UL19 1/20 0.53
MAOA P21397 3/20 0.51
NPC1 O15118 1/20 0.51
ALDH1A1 P00352 1/20 0.51
LMNA P02545 1/20 0.51
MAPT P10636 1/20 0.51
HTT P42858 1/20 0.51
RAB9A P51151 1/20 0.51
SMN1; SMN2 Q16637 1/20 0.51
KDM4E B2RXH2 1/20 0.51
MMP1 P03956 2/20 0.50
MMP2 P08253 2/20 0.50

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
SCHEMBL8464563 1.00 CYP1A2 (0.67) CYP1A2MAOBHDAC2CYP1B1CXCL12
SCHEMBL1620259 1.00 CYP1A2 (0.67) CYP1A2MAOBHDAC2CYP1B1CXCL12
SCHEMBL27685617 0.98 CYP1A2 (0.64) CYP1A2MAOBHDAC2CYP1B1CXCL12
SCHEMBL28347012 0.89 CYP1A2 (0.75) CYP1A2MAOBHDAC2CYP1B1CXCL12
SCHEMBL126171 0.83 CYP1A2 (0.72) CYP1A2MAOBHDAC2CYP1B1CXCL12
SCHEMBL269140 0.83 CYP1A2 (0.72) CYP1A2MAOBHDAC2CYP1B1CXCL12
SCHEMBL4732055 0.83 CYP1A2 (0.72) CYP1A2MAOBHDAC2CYP1B1CXCL12
SCHEMBL11452510 0.81 CYP1A2 (0.69) CYP1A2MAOBHDAC2CYP1B1CXCL12
Hydrochloric Acid SCHEMBL27093050 0.81 CYP1A2 (0.69) CYP1A2MAOBHDAC2CYP1B1CXCL12
Hydrochloric Acid SCHEMBL5929339 0.81 CYP1A2 (0.69) CYP1A2MAOBHDAC2CYP1B1CXCL12

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-120040348-A Preparation method for efficiently synthesizing CB1 antagonist pyrazole derivative 中国药科大学 2025-05-27 CN disclosed
US-20140273130-A1 COMPETITIVE GROWTH AND/OR PRODUCTION ADVANTAGE FOR BUTANOLOGEN MICROORGANISM BUTAMAX ADVANCED BIOFUELS LLC (US) 2014-09-18 US disclosed
EP-1626963-B1 Substituted pyrazoline compounds, their preparation and use as medicaments ESTEVE LABOR DR (ES) 2012-08-15 EP disclosed
US-8207156-B2 Substituted pyrazoline compounds, their preparation and use as medicaments LABORATORIOS DEL DR. ESTEVE, S.A. (ES) 2012-06-26 US disclosed
EP-1910299-B1 SUBSTITUTED PYRAZOLINE COMPOUNDS, THEIR PREPARATION AND USE AS MEDICAMENTS ESTEVE LABOR DR (ES) 2011-09-07 EP disclosed
US-7998996-B2 Controlling triglyceride concentration; central nervous system disorders; psychological disorders; eating disordes; drug abuse; anticancer agents LABORATORIOS DEL DR. ESTEVE S.A. (ES) 2011-08-16 US disclosed
US-20110160459-A1 5-ARYL-4,5-DIHYDRO-(1H)-PYRAZOLINES AS CANNABINOID CB1 RECEPTOR AGONISTS SOLVAY PHARMACEUTICALS, B.V. 2011-06-30 US disclosed
US-20110160181-A1 SUBSTITUTED PYRAZOLINE COMPOUNDS, THEIR PREPARATION AND USE AS MEDICAMENTS LABORATORIOS DEL DR. ESTEVE, S.A. (ES) 2011-06-30 US disclosed
US-7968582-B2 5(S)-substituted pyrazoline compounds, their preparation and use as medicaments LABOROTORIOS DEL DR. ESTEVE, S.A. (ES) 2011-06-28 US disclosed
US-7928134-B2 5-aryl-4,5-dihydro-(1H)-pyrazolines as cannabinoid CB1 receptor agonists SOLVAY PHARMACEUTICALS B.V. (NL) 2011-04-19 US disclosed
EP-1718619-A1 SUBSTITUTED PYRAZOLINE COMPOUNDS FOR REDUCING TRIGLYCERIDES IN BLOOD Laboratorios del Dr. Esteve S.A. (ES) 2006-11-08 EP disclosed
US-20060189658-A1 Substituted pyrazoline compounds, their preparation and use as medicaments LABORATORIOS DR. ESTEVE S.A. (ES) 2006-08-24 US disclosed
EP-1637522-A1 Substituted pyrazoline compounds for reducing triglycerides in blood LABORATORIOS DEL DR. ESTEVE, S.A. (ES) 2006-03-22 EP disclosed
EP-1626963-A1 SUBSTITUTED PYRAZOLINE COMPOUNDS, THEIR PREPARATION AND USE AS MEDICAMENTS LABORATORIOS DEL DR. ESTEVE, S.A. (ES) 2006-02-22 EP disclosed
US-20060020010-A1 Substituted pyrazoline compounds, their preparation and use as medicaments ESTEVE PHARMACEUTICALS, S.A. (ES) 2006-01-26 US disclosed
WO-2005077911-A1 SUBSTITUTED PYRAZOLINE COMPOUNDS, THEIR PREPARATION AND USE AS MEDICAMENTS LABORATORIOS DEL DR. ESTEVE S.A. (ES) 2005-08-25 WO disclosed
WO-2005077909-A1 SUBSTITUTED PYRAZOLINE COMPOUNDS FOR REDUCING TRIGLYCERIDES IN BLOOD LABORATORIOS DR. ESTEVE S.A. (ES) 2005-08-25 WO disclosed
US-6204220-B1 AS HERBICIDES FOR CONTROLLING UNWANTED VEGETATION RUTGERS, THE STATE UNIVERSITY OF NEW JERSEY 2001-03-20 US disclosed
EP-0387058-A1 Process for preparing benzylpyruvic acids and esters MERCK & CO. INC. (US) 1990-09-12 EP disclosed
US-4956490-A Process for preparing benzylpyruvic acids and esters MERCK & CO., INC. (US) 1990-09-11 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 (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-20060020010-A1 Substituted pyrazoline compounds, their preparation and use as medicaments PIR, SYMPK, P2RX5 CYP1A2 110/4885MAOB 798/4885HDAC2 715/4885
US-20060189658-A1 Substituted pyrazoline compounds, their preparation and use as medicaments PIR, SYMPK, P2RX5 CYP1A2 110/4885MAOB 798/4885HDAC2 715/4885
US-20110160459-A1 5-ARYL-4,5-DIHYDRO-(1H)-PYRAZOLINES AS CANNABINOID CB1 RECEPTOR AGONISTS CNR1, CNR2, HTR5A CYP1A2 273/4885MAOB 1112/4885HDAC2 2169/4885
US-20110160181-A1 SUBSTITUTED PYRAZOLINE COMPOUNDS, THEIR PREPARATION AND USE AS MEDICAMENTS PIR, SYMPK, P2RX5 CYP1A2 110/4885MAOB 798/4885HDAC2 715/4885

“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.