Oxalic Acid

Oxalic Acid

SCHEMBL198073

Nc1ccsc1.O=C(O)C(=O)O

nearest known ligand 0.48

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

OPRM1SLC6A4

The experimentally established mechanism targets of Oxalic Acid. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
LCK P06239 1/20 0.48
FYN P06241 1/20 0.48
DAO P14920 1/20 0.48
CES2 O00748 1/20 0.44
CES1 P23141 1/20 0.44
IKBKB O14920 2/20 0.41
MAPT P10636 2/20 0.41
ALDH1A1 P00352 1/20 0.41
HDAC6 Q9UBN7 1/20 0.41
HDAC1 Q13547 1/20 0.39
HPGD P15428 1/20 0.37
SLC1A3 P43003 2/20 0.36
SLC1A2 P43004 2/20 0.36
SLC1A1 P43005 2/20 0.36
PTPRF P10586 1/20 0.36
PTPN1 P18031 1/20 0.36
ADRA2A P08913 2/20 0.35
ADRA2B P18089 2/20 0.35
ADRA2C P18825 2/20 0.35
ACMSD Q8TDX5 1/20 0.35

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
Oxalic Acid SCHEMBL27649777 1.00 LCK (0.48) LCKFYNDAOCES2CES1
SCHEMBL27445546 0.86 LCK (0.41) LCKFYNDAOCES2CES1
SCHEMBL129324 0.84
SCHEMBL29575307 0.82
SCHEMBL28199189 0.82
Hydrochloric Acid SCHEMBL1031787 0.82
Phosphoric Acid SCHEMBL1094050 0.81 CES2 (0.39) LCKFYNDAOCES2CES1
Phosphonic Acid SCHEMBL27762789 0.81 CES2 (0.39) LCKFYNDAOCES2CES1
Cyclopropanecarboxylic Acid Amide SCHEMBL28410835 0.76 SMN1; SMN2 (0.42) LCKFYNDAOCES2CES1
Propane SCHEMBL6193423 0.75

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-115974833-B Preparation method of 3-aminothiophene oxalate 苏州汉德创宏生化科技有限公司 2024-08-02 CN claimed
CN-115974833-A Preparation method of 3-aminothiophene oxalate 苏州汉德创宏生化科技有限公司 2023-04-18 CN claimed
CN-111072930-B Fluorine-containing thiophene derivative polymer film PEDOT-F, and preparation method and application thereof 浙江工业大学 2022-05-24 CN claimed
CN-111072930-A Fluorine-containing thiophene derivative polymer film PEDOT-F, and preparation method and application thereof 浙江工业大学 2020-04-28 CN claimed
CN-111018828-A Fluorine-containing thiophene derivative 3- (N-trifluoroacetylamino) thiophene and synthetic method and application thereof 浙江工业大学 2020-04-17 CN claimed
CN-108727414-A A kind of unsubstituted thiophene bioxindol class compounds of N- and preparation method thereof 中国科学院青岛生物能源与过程研究所 2018-11-02 CN claimed
US-20250243202-A1 Compounds Useful as RET Inhibitors CANCER RESEARCH TECHNOLOGY LIMITED (GB) 2025-07-31 US disclosed
EP-4567035-A1 NOVEL COMPOUND AS HYPOXIA-INDUCIBLE FACTOR 1(HIF-1) INHIBITOR OR VASCULAR ENDOTHELIAL GROWTH FACTOR (VEGF) INHIBITOR, AND PHARMACEUTICAL COMPOSITION COMPRISING SAME Nextgen Bioscience Co., Ltd. (KR) 2025-06-11 EP disclosed
CN-119654324-A Novel compounds as hypoxia inducible factor 1 (HIF-1) inhibitors or Vascular Endothelial Growth Factor (VEGF) inhibitors and pharmaceutical compositions comprising the same 株式会社次代生物科学 2025-03-18 CN disclosed
CN-119161353-A Design, synthesis and activity evaluation of pyranopyrimidine heterocyclic p97/VCP inhibitors 首都医科大学 2024-12-20 CN disclosed
CN-115974833-B Preparation method of 3-aminothiophene oxalate 苏州汉德创宏生化科技有限公司 2024-08-02 CN disclosed
CN-115974833-B Preparation method of 3-aminothiophene oxalate 苏州汉德创宏生化科技有限公司 2024-08-02 CN disclosed
CN-115974833-B Preparation method of 3-aminothiophene oxalate 苏州汉德创宏生化科技有限公司 2024-08-02 CN disclosed
US-20030153595-A1 Azabicyclic-substituted fused-heteroaryl compounds for the treatment of disease PHARMACIA & UPJOHN COMPANY 2003-08-14 US disclosed
WO-2003029252-A1 AZABICYCLIC-SUBSTITUTED FUSED-HETEROARYL COMPOUNDS FOR THE TREATMENT OF DISEASE PHARMACIA & UPJOHN COMPANY (US) 2003-04-10 WO disclosed
US-20030045540-A1 Quinuclidines-substituted-multi-cyclic-heteroaryls for the treatment of disease PHARMACIA & UPJOHN COMPANY 2003-03-06 US disclosed
WO-2002100857-A1 QUINUCLIDINES-SUBSTITUTED-MULTI-CYCLIC-HETEROARYLS FOR THE TREATMENT OF DISEASE PHARMACIA & UPJOHN COMPANY (US) 2002-12-19 WO disclosed
US-6331639-B2 BY REACTING A 3-((ALKYL, ALKOXY, PHENYL OR HETEROARYL)CARBONYLAMINO)THIOPHENE WITH A KETONE IN THE PRESENCE OF AN ACID AND REDUCING THE REACTION MIXTURE; AGRICULTURAL FUNGICIDES MITSUI CHEMICALS, INC. (JP) 2001-12-18 US disclosed
US-20010023295-A1 Process for preparing 2-alkyl-3-aminothiophene derivative and 3-aminothiophene derivative KATSUTA HIROYUKI (JP) 2001-09-20 US disclosed
US-6239282-B1 ALKYLATING THE CORRESPONDING 3-AMIDOTHIOPHENE COMPOUND MITSUI CHEMICALS, INC. (JP) 2001-05-29 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-20010023295-A1 Process for preparing 2-alkyl-3-aminothiophene derivative and 3-aminothiophene derivative SULT1E1, CYP4B1, CYP3A4 LCK 3145/4885FYN 2289/4885DAO 37/4885
US-20030153595-A1 Azabicyclic-substituted fused-heteroaryl compounds for the treatment of disease MALT1, TPMT, ABCB1 LCK 1455/4885FYN 1649/4885DAO 659/4885
US-20030045540-A1 Quinuclidines-substituted-multi-cyclic-heteroaryls for the treatment of disease NQO2, SLC10A1, CYP7A1 LCK 3015/4885FYN 2637/4885DAO 1489/4885
US-20250243202-A1 Compounds Useful as RET Inhibitors RET, BCR, REL LCK 43/4885FYN 30/4885DAO 1914/4885

“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.