SCHEMBL2414698

SCHEMBL2414698

CCC(F)(C(C)=O)C(=O)O

nearest known ligand 0.36

Predicted protein targets (top 12)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 3/20 0.32
MEN1 O00255 1/20 0.32
CYP1A2 P05177 1/20 0.32
THRB P10828 1/20 0.32
KMT2A Q03164 1/20 0.32
FFAR3 O14843 2/20 0.32
TDP1 Q9NUW8 1/20 0.32
TSHR P16473 1/20 0.30
ACLY P53396 2/20 0.30
FAAH O00519 1/20 0.30
LCK P06239 1/20 0.30
FYN P06241 1/20 0.30

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
SCHEMBL19227950 0.86 ALDH1A1 (0.37) ALDH1A1MEN1CYP1A2KMT2AFFAR3
SCHEMBL19607726 0.86 FFAR3 (0.37) ALDH1A1MEN1CYP1A2THRBKMT2A
SCHEMBL29186815 0.83 FFAR3 (0.35) ALDH1A1MEN1CYP1A2THRBKMT2A
SCHEMBL6902951 0.77 CES2 (0.39) ALDH1A1MEN1CYP1A2THRBKMT2A
SCHEMBL4384467 0.75 FAAH (0.32) ALDH1A1MEN1CYP1A2THRBKMT2A
Lithium Ion SCHEMBL25327835 0.73
SCHEMBL5566630 0.73 CES2 (0.30)
SCHEMBL16681682 0.72 ALDH1A1 (0.37) ALDH1A1TSHR
SCHEMBL7622632 0.72 SOAT1 (0.41) ALDH1A1MEN1THRBKMT2A
SCHEMBL19582468 0.70 CES2 (0.37) ALDH1A1MEN1CYP1A2THRBKMT2A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-108218702-B Preparation method of 2-fluoro ethyl acetoacetate 湖北卓熙氟化股份有限公司 2020-10-09 CN claimed
CN-108218702-B Preparation method of 2-fluoro ethyl acetoacetate 湖北卓熙氟化股份有限公司 2020-10-09 CN disclosed
US-10112973-B2 Process for the preparation of ramipril SANOFI-AVENTIS DEUTSCHLAND GMBH (DE) 2018-10-30 US disclosed
EP-3154940-B1 PROCESS FOR THE PREPARATION OF RAMIPRIL SANOFI AVENTIS DEUTSCHLAND (DE) 2018-04-18 EP disclosed
EP-2549991-B1 FE(III) COMPLEX COMPOUNDS FOR TREATING AND PROPHYLAXIS FOR ANAEMIA SYMPTOMS AND ANAEMIA VIFOR (INTERNATIONAL) AG (CH) 2017-11-22 EP disclosed
US-20170158733-A1 PROCESS FOR THE PREPARATION OF RAMIPRIL SANOFI-AVENTIS DEUTSCHLAND GMBH (DE) 2017-06-08 US disclosed
EP-3154940-A1 PROCESS FOR THE PREPARATION OF RAMIPRIL Sanofi-Aventis Deutschland GmbH (DE) 2017-04-19 EP disclosed
WO-2015189108-A1 PROCESS FOR THE PREPARATION OF RAMIPRIL SANOFI-AVENTIS DEUTSCHLAND GMBH (DE) 2015-12-17 WO disclosed
EP-2549991-A1 FE(III) COMPLEX COMPOUNDS FOR THE TREATMENT AND PROPHYLAXIS OF IRON DEFICIENCY SYMPTOMS AND IRON DEFICIENCY ANEMIAS Vifor (International) AG (CH) 2013-01-30 EP disclosed
WO-2011117225-A1 FE(III) COMPLEX COMPOUNDS FOR THE TREATMENT AND PROPHYLAXIS OF IRON DEFICIENCY SYMPTOMS AND IRON DEFICIENCY ANEMIAS VIFOR (INTERNATIONAL) AG (CH) 2011-09-29 WO disclosed
US-20050007872-A1 Microdevice FUJI PHOTO FILM CO., LTD. 2005-01-13 US disclosed
EP-1481724-A1 Reaction method using microreactor Fuji Photo Film Co., Ltd. (JP) 2004-12-01 EP disclosed
EP-1481723-A1 Microdevice Fuji Photo Film Co., Ltd. (JP) 2004-12-01 EP disclosed
EP-1095928-B1 Direct fluorination process for preparing high purity alpha-fluoro-beta-dicarbonyl compounds AIR PROD & CHEM (US) 2004-02-04 EP disclosed
US-6455728-B1 REACTING METHYL-3-OXOPENTANOATE WTIH HYDROGEN FLUORIDE IN PRESENCE OF OXYGEN; BY-PRODUCT INHIBITION; CHEMICAL INTERMEDIATES FOR PRODUCING PHARMACEUTICALS AIR PRODUCTS AND CHEMICALS, INC. 2002-09-24 US disclosed
EP-0996606-B1 CATALYSED FLUORINATION OF CARBONYL COMPOUNDS F2 CHEMICALS LTD (GB) 2002-01-16 EP disclosed
US-6300511-B1 FLUORINATING CARBONYL COMPOUND BY REPLACEMENT OF ALPHA-HYDROGEN ATOM WITH FLUORINE COMPRISING REACTING COMPOUND WITH FLUORINATING AGENT IN PRESENCE OF CATALYTICALLY EFFECTIVE AMOUNT OF TRANSITION METAL-CONTAINING CATALYST F2 CHEMICALS LIMITED (GB) 2001-10-09 US disclosed
EP-1095928-A2 Direct fluorination process for preparing high purity alpha-fluoro-beta-dicarbonyl compounds AIR PRODUCTS AND CHEMICALS, INC. (US) 2001-05-02 EP disclosed
EP-0996606-A1 CATALYSED FLUORINATION OF CARBONYL COMPOUNDS F2 Chemicals Ltd. (GB) 2000-05-03 EP disclosed
WO-1999003802-A1 CATALYSED FLUORINATION OF CARBONYL COMPOUNDS F2 CHEMICALS LIMITED (GB) 1999-01-28 WO 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-10112973-B2 Process for the preparation of ramipril CYP2S1, CYP3A5, CYP4B1 ALDH1A1 162/4885MEN1 4797/4885CYP1A2 4/4885
US-20170158733-A1 PROCESS FOR THE PREPARATION OF RAMIPRIL CYP2S1, CYP3A5, CYP4B1 ALDH1A1 162/4885MEN1 4797/4885CYP1A2 4/4885

“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.