Formic Acid

Formic Acid

SCHEMBL2368233

CCCCN(CCCC)CCCC.O=CO

nearest known ligand 0.46

Full drug profile on Sugi Atlas →

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CA12 O43570 2/20 0.46
CA1 P00915 2/20 0.46
CA9 Q16790 2/20 0.46
KDM5A P29375 4/20 0.42
PHF8 Q9UPP1 2/20 0.40
KDM4C Q9H3R0 2/20 0.40
TSHR P16473 2/20 0.39
MMP1 P03956 1/20 0.38
MMP2 P08253 1/20 0.38
MMP3 P08254 1/20 0.38
MMP8 P22894 1/20 0.38
THRA P10827 2/20 0.37
THRB P10828 2/20 0.37
LMNA P02545 1/20 0.37
CYP1A2 P05177 1/20 0.37
CHRM2 P08172 1/20 0.37
CYP3A4 P08684 1/20 0.37
HTR1A P08908 1/20 0.37
GAA P10253 1/20 0.37
CYP2D6 P10635 1/20 0.37

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
Formic Acid SCHEMBL9721362 0.97 CA12 (0.44) CA12CA1CA9KDM5APHF8
Formic Acid SCHEMBL1131732 0.91 CA12 (0.40) CA12CA1CA9KDM5APHF8
Formic Acid SCHEMBL2867086 0.90 DNM1 (0.46) CA12CA1CA9KDM5APHF8
Formic Acid SCHEMBL28121779 0.90 DNM1 (0.46) CA12CA1CA9KDM5APHF8
Formic Acid SCHEMBL4355881 0.82 CA12 (0.42) CA12CA1CA9TSHRCYP3A4
Hydrogen Peroxide SCHEMBL137833 0.82 KDM5A (0.48) CA12CA1CA9KDM5APHF8
Methyl Alcohol SCHEMBL3078253 0.82 CA12 (0.48) CA12CA1CA9KDM5APHF8
Hydrogen Peroxide SCHEMBL137835 0.82 KDM5A (0.48) CA12CA1CA9KDM5APHF8
SCHEMBL3904839 0.82 TSHR (0.46) CA12CA1CA9KDM5APHF8
SCHEMBL27566038 0.82 TSHR (0.46) CA12CA1CA9KDM5APHF8

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-115340446-A Chiral benzocyclobutene alcohol, and synthesis method and application thereof 复旦大学 2022-11-15 CN claimed
EP-2821399-A1 Method for preparation of 6-trifluoromethylpyridine-3-carboxylic acid derivatives from 4,4,4-trifluoro-3-oxobutanoyl chloride Lonza Ltd (CH) 2015-01-07 EP claimed
EP-2818461-A1 Method for preparation of 6-trifluoromethylpyridine-3-carboxylic acid derivatives from 4,4,4-trifluoro-3-oxobutanoyl chloride Lonza Ltd (CH) 2014-12-31 EP claimed
US-20130096346-A1 RESOLUTION METHODS FOR ISOLATING DESIRED ENANTIOMERS OF TAPENTADOL INTERMEDIATES AND USE THEREOF FOR THE PREPARATION OF TAPENTADOL ACTAVIS GROUP PTC EHF (IS) 2013-04-18 US claimed
EP-2542521-A2 IMPROVED RESOLUTION METHODS FOR ISOLATING DESIRED ENANTIOMERS OF TAPENTADOL INTERMEDIATES AND USE THEREOF FOR THE PREPARATION OF TAPENTADOL Actavis Group Ptc Ehf (IS) 2013-01-09 EP claimed
US-20110318417-A1 HIGHLY PURE CINACALCET OR A PHARMACEUTICALLY ACCEPTABLE SALT THEREOF ACTAVIS GROUP PTC EHF (IS) 2011-12-29 US claimed
EP-2376424-A1 HIGHLY PURE CINACALCET OR A PHARMACEUTICALLY ACCEPTABLE SALT THEREOF Actavis Group PTC EHF (IS) 2011-10-19 EP claimed
WO-2011107876-A2 IMPROVED RESOLUTION METHODS FOR ISOLATING DESIRED ENANTIOMERS OF TAPENTADOL INTERMEDIATES AND USE THEREOF FOR THE PREPARATION OF TAPENTADOL ACTAVIS GROUP PTC EHF (IS) 2011-09-09 WO claimed
WO-2010067204-A1 HIGHLY PURE CINACALCET OR A PHARMACEUTICALLY ACCEPTABLE SALT THEREOF ACTAVIS GROUP PTC EHF (IS) 2010-06-17 WO claimed
US-20250242275-A1 APPARATUS AND METHOD FOR PROCESSING A BIOMASS MATERIAL BUSS-SMS-CANZLER GMBH (DE) 2025-07-31 US disclosed
US-20250145889-A1 METHOD FOR PROCESSING A BIOMASS MATERIAL PROIONIC GMBH (AT) 2025-05-08 US disclosed
CN-118804981-A Method for processing biomass material 普罗奥尼克股份有限公司 2024-10-18 CN disclosed
EP-4377467-A2 METHOD FOR PROCESSING A BIOMASS MATERIAL proionic GmbH (AT) 2024-06-05 EP disclosed
WO-2023084131-A2 METHOD FOR PROCESSING A BIOMASS MATERIAL PROIONIC GMBH (AT) 2023-05-19 WO disclosed
CN-1249045-C Process for preparing isoflavones DSM IP ASSETS BV (NL) 2006-04-05 CN disclosed
CN-1505621-A Process for the preparation of isoflavones DSM IP �ʲ����޹�˾ 2004-06-16 CN disclosed
US-20030091838-A1 Composition for film formation, method of film formation, and silica-based film JSR CORPORATION (JP) 2003-05-15 US disclosed
EP-0429995-B1 Process for hydrogenation of oils HELIOS OLJARNA DOMZALE D O O (YU) 1996-02-28 EP disclosed
EP-0429995-A2 Process for hydrogenation of oils HELIOS OLJARNA DOMZALE d.o.o. (YU) 1991-06-05 EP disclosed
US-4334117-A DIMERIZATION OF BUTADIENE/1,3-/ AND ISOPRENE KURARAY CO., LTD. (JP) 1982-06-08 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-20110318417-A1 HIGHLY PURE CINACALCET OR A PHARMACEUTICALLY ACCEPTABLE SALT THEREOF H4C1; H4C2; H4C3; H4C4; H4C5; H4C6; H4C8; H4C9; H4C11; H4C12; H4C13; H4C14; H4C15; H4C16, REN, SLC6A12 CA12 173/4885CA1 1068/4885CA9 25/4885
US-20130096346-A1 RESOLUTION METHODS FOR ISOLATING DESIRED ENANTIOMERS OF TAPENTADOL INTERMEDIATES AND USE THEREOF FOR THE PREPARATION OF TAPENTADOL OPRD1, OPRK1, OPRM1 CA12 2890/4885CA1 2183/4885CA9 1782/4885

“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.