Oxalic Acid

Oxalic Acid

SCHEMBL890984

CC(C)O.O=C(O)C(=O)O

nearest known ligand 0.57

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 8)

geneUniProtsupporting neighboursconfidence
TP53 P04637 1/20 0.57
ALDH1A1 P00352 1/20 0.55
LMNA P02545 1/20 0.55
TSHR P16473 1/20 0.40
FFAR3 O14843 1/20 0.39
LCK P06239 1/20 0.39
FYN P06241 1/20 0.39
SLC7A5 Q01650 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
Oxalic Acid SCHEMBL28595430 0.91 TP53 (0.57) TP53ALDH1A1LMNATSHRFFAR3
Oxalic Acid SCHEMBL3973877 0.86 TP53 (0.50) TP53ALDH1A1FFAR3LCKFYN
Isopropyl Alcohol SCHEMBL9737750 0.86
Isopropyl Alcohol SCHEMBL538205 0.86 TP53 (0.61) TP53ALDH1A1LMNATSHRFFAR3
Isopropyl Alcohol SCHEMBL3155394 0.86 TP53 (0.61) TP53ALDH1A1LMNATSHRFFAR3
Lactic Acid SCHEMBL9435530 0.84 TP53 (0.85) TP53ALDH1A1LMNATSHRSLC7A5
Oxalic Acid SCHEMBL1837929 0.84 TP53 (0.50) TP53SLC7A5
Acetic Acid SCHEMBL9659096 0.82 FFAR3 (0.64) TP53ALDH1A1LMNATSHRFFAR3
Acetic Acid SCHEMBL574619 0.82 FFAR3 (0.64) TP53ALDH1A1LMNATSHRFFAR3
Isopropyl Alcohol SCHEMBL15251690 0.82 TP53 (0.57) TP53ALDH1A1LMNATSHRFFAR3

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-105161686-B Rich lithium material of manganese basic unit shape of double-coating and preparation method thereof 华南师范大学 2017-09-15 CN claimed
CN-115485276-B Deuterated AKT kinase inhibitors 南京正大天晴制药有限公司 2024-05-31 CN disclosed
CN-117964620-A AKT inhibitors 南京正大天晴制药有限公司 2024-05-03 CN disclosed
CN-115843298-B Salts and crystal forms of dihydropyrido [2,3-d ] pyrimidinone derivative 南京正大天晴制药有限公司 2024-03-29 CN disclosed
CN-113272304-B AKT inhibitors 南京正大天晴制药有限公司 2024-03-29 CN disclosed
CN-115836069-B Salts of dihydropyrido [2,3-d ] pyrimidinone derivatives, preparation method and application thereof 南京正大天晴制药有限公司 2024-02-06 CN disclosed
US-20230321108-A1 UNIT DOSAGE COMPOSITION OF AKT INHIBITOR NANJING CHIA TAI TIANQING PHARMACEUTICAL CO., LTD. (CN) 2023-10-12 US disclosed
US-20230286979-A1 SALT OF DIHYDROPYRIDO[2,3-D]PYRIMIDINONE DERIVATIVE, PREPARATION METHOD THEREFOR, AND USE THEREOF NANJING CHIA TAI TIANQING PHARMACEUTICAL CO., LTD. (CN) 2023-09-14 US disclosed
US-20230271958-A1 SALT AND CRYSTAL FORM OF DIHYDROPYRIDO[2,3-d]PYRIMIDINE DERIVATE NANJING CHIA TAI TIANQING PHARMACEUTICAL CO., LTD. (CN) 2023-08-31 US disclosed
EP-4186902-A1 SALT OF DIHYDROPYRIDO[2,3-D]PYRIMIDINONE DERIVATIVE, PREPARATION METHOD THEREFOR, AND USE THEREOF Nanjing Chia Tai Tianqing Pharmaceutical Co., Ltd. (CN) 2023-05-31 EP disclosed
CN-101014570-A Piperidine derivative or pharmaceutically acceptable salt thereof ASTELLAS PHARMA INC (JP) 2007-08-08 CN disclosed
US-6489322-B1 BENZOXAZEPINES AS SELECTIVE INHIBITORS OF THE NEURONAL ISOFORM OF NITRIC OXIDE SYNTHASE FOR TREATMENT OF NEURODEGENERATIVE DISEASE ASTRAZENECA AB (SE) 2002-12-03 US disclosed
EP-0983268-B1 AMIDINE DERIVATIVES AS INHIBITORS OF NITRIC OXIDE SYNTHASE ASTRAZENECA AB (SE) 2002-07-24 EP disclosed
CN-1358169-A N-alkoxyalkyl-N,N-dialkylamine derivatives or salts thereof, and remedies for nerve degeneration diseases containing the same TOYAMA CHEMICAL CO LTD (JP) 2002-07-10 CN disclosed
CN-1314616-A Imaging element including support and mechanical holder EASTMAN KODAK CO (US) 2001-09-26 CN disclosed
EP-0983268-A1 AMIDINE DERIVATIVES AS INHIBITORS OF NITRIC OXIDE SYNTHASE Astra Aktiebolag (SE) 2000-03-08 EP disclosed
WO-1998050382-A1 AMIDINE DERIVATIVES AS INHIBITORS OF NITRIC OXIDE SYNTHASE ASTRA AKTIEBOLAG (SE) 1998-11-12 WO disclosed
CN-1178530-A Compounds having an effect on 5-hydroxytryptamine related systems LILLY CO ELI (US) 1998-04-08 CN disclosed
US-4863949-A CARDIOVASCULAR DISORDER TREATMENT BOEHRINGER MANNHEIM GMBH (DE) 1989-09-05 US disclosed
US-4435048-A LARGE AREA OPTICAL DISPLAY ASAHI GLASS COMPANY LTD. (JP) 1984-03-06 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 (3 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-20230321108-A1 UNIT DOSAGE COMPOSITION OF AKT INHIBITOR AKT2, AKT1, PIK3R2 TP53 1481/4885ALDH1A1 4415/4885LMNA 3471/4885
US-20230286979-A1 SALT OF DIHYDROPYRIDO[2,3-D]PYRIMIDINONE DERIVATIVE, PREPARATION METHOD THEREFOR, AND USE THEREOF FH, GRHPR, SDHB TP53 214/4885ALDH1A1 492/4885LMNA 4812/4885
US-20230271958-A1 SALT AND CRYSTAL FORM OF DIHYDROPYRIDO[2,3-d]PYRIMIDINE DERIVATE DCK, DPYD, UCK2 TP53 1846/4885ALDH1A1 1413/4885LMNA 4339/4885

“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.