Arundic Acid

Arundic Acid

SCHEMBL3450562

CCCCCC[C@H](CCC)C(=O)O

nearest known ligand 0.73

Full drug profile on Sugi Atlas →

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CHRM1 P11229 1/20 0.73
AKR1A1 P14550 1/20 0.73
CHRM3 P20309 1/20 0.73
HTR2A P28223 1/20 0.73
HTR2C P28335 1/20 0.73
ADRA1A P35348 1/20 0.73
HRH1 P35367 1/20 0.73
DRD3 P35462 1/20 0.73
SLC6A3 Q01959 1/20 0.73
HDAC1 Q13547 1/20 0.73
HDAC2 Q92769 1/20 0.73
TDP1 Q9NUW8 1/20 0.73
GRIK1 P39086 3/20 0.63
GRIK2 Q13002 3/20 0.63
CA2 P00918 2/20 0.61
MAPK1 P28482 1/20 0.61
SLC1A2 P43004 3/20 0.60
SLC1A1 P43005 3/20 0.60
GPR84 Q9NQS5 6/20 0.59
FFAR1 O14842 1/20 0.59

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
SCHEMBL1943942 1.00 CHRM1 (0.73) CHRM1AKR1A1CHRM3HTR2AHTR2C
SCHEMBL1115851 1.00 CHRM1 (0.73) CHRM1AKR1A1CHRM3HTR2AHTR2C
Arundic Acid SCHEMBL277260 1.00 CHRM1 (0.73) CHRM1AKR1A1CHRM3HTR2AHTR2C
SCHEMBL3630645 1.00 CHRM1 (0.73) CHRM1AKR1A1CHRM3HTR2AHTR2C
SCHEMBL2489255 1.00 CHRM1 (0.73) CHRM1AKR1A1CHRM3HTR2AHTR2C
SCHEMBL1115797 1.00 CHRM1 (0.73) CHRM1AKR1A1CHRM3HTR2AHTR2C
SCHEMBL15499898 1.00 CHRM1 (0.73) CHRM1AKR1A1CHRM3HTR2AHTR2C
SCHEMBL432094 1.00 CHRM1 (0.73) CHRM1AKR1A1CHRM3HTR2AHTR2C
SCHEMBL1115939 1.00 CHRM1 (0.73) CHRM1AKR1A1CHRM3HTR2AHTR2C
SCHEMBL1115977 1.00 CHRM1 (0.73) CHRM1AKR1A1CHRM3HTR2AHTR2C

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-100430364-C Preparation method of (2R) -2-propyl octanoic acid ONO PHARMACEUTICAL CO (JP) 2008-11-05 CN claimed
CN-101100422-A Process for the preparation of (2R)-2-propyloctanoic acid ONO PHARMACEUTICAL CO (JP) 2008-01-09 CN claimed
US-20070043114-A1 Nerve regeneration promoters ONO PHARMACEUTICAL CO., LTD. (JP) 2007-02-22 US claimed
EP-1685832-A1 NERVE REGENERATION PROMOTERS ONO PHARMACEUTICAL CO., LTD. (JP) 2006-08-02 EP claimed
US-10000432-B2 Processes for the synthesis of chiral 1-alkanols PURDUE RESEARCH FOUNDATION (US) 2018-06-19 US disclosed
US-10000432-B2 Processes for the synthesis of chiral 1-alkanols PURDUE RESEARCH FOUNDATION (US) 2018-06-19 US disclosed
EP-3094613-A1 PROCESSES FOR THE SYNTHESIS OF CHIRAL 1-ALKANOLS Purdue Research Foundation, Inc. (US) 2016-11-23 EP disclosed
US-20160332940-A1 PROCESSES FOR THE SYNTHESIS OF CHIRAL 1-ALKANOLS PURDUE RESEARCH FOUNDATION (US) 2016-11-17 US disclosed
US-20160332940-A1 PROCESSES FOR THE SYNTHESIS OF CHIRAL 1-ALKANOLS PURDUE RESEARCH FOUNDATION (US) 2016-11-17 US disclosed
WO-2015106045-A1 PROCESSES FOR THE SYNTHESIS OF CHIRAL 1-ALKANOLS PURDUE RESEARCH FOUNDATION (US) 2015-07-16 WO disclosed
US-8569058-B2 Nerve regeneration promoters ONO PHARMACEUTICAL CO., LTD. (JP) 2013-10-29 US disclosed
EP-1741697-B1 CRYSTAL COMPRISING (2R)-2-PROPYLOCTANOIC ACID AND DIBENZYLAMINE ONO PHARMACEUTICAL CO (JP) 2012-12-19 EP disclosed
US-20060135802-A1 Process for producing (2r)-2-propyloctanoic acid and intermediate therefor ONO PHARMACEUTICAL CO., LTD. (JP) 2006-06-22 US disclosed
CN-1144796-C Intermediates and process for preparation of optically active octanoic acid derivs. СҰҩƷ��ҵ��ʽ���� 2004-04-07 CN disclosed
EP-1078921-B1 NOVEL INTERMEDIATES AND PROCESSES FOR THE PREPARATION OF OPTICALLY ACTIVE OCTANOIC ACID DERIVATIVES ONO PHARMACEUTICAL CO (JP) 2003-03-26 EP disclosed
US-6392073-B1 IMPROVED OPTICAL PURITY OVER RECRYSTALLIZATION METHOD; 2.10 CAMPHORSULTAM DERIVATIVE ONO PHARMACEUTICAL CO., LTD. (JP) 2002-05-21 US disclosed
US-20020028947-A1 Novel intermediates and processes for the preparation of optically active octanoic acid derivatives ONO PHARMACEUTICAL CO., LTD. 2002-03-07 US disclosed
US-6333415-B1 N-(2S-(2-(PROPENYL OR PROPYNYL OR PROPYL)) OCTANOYL) (1S)-(-)-2,10-CAMPHORSULTAM, TO PREPARE 2S-(2-(PROPENYL OR PROPYNYL OR PROPYL)) OCTANOIC ACID, ONO PHARMACEUTICAL CO., LTD. (JP) 2001-12-25 US disclosed
CN-1309652-A Intermediates and process for preparation of optically active octanoic acid derivs. ONO PHARMACEUTICAL CO (JP) 2001-08-22 CN disclosed
EP-1078921-A1 NOVEL INTERMEDIATES AND PROCESSES FOR THE PREPARATION OF OPTICALLY ACTIVE OCTANOIC ACID DERIVATIVES ONO PHARMACEUTICAL CO., LTD. (JP) 2001-02-28 EP 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 (5 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-20070043114-A1 Nerve regeneration promoters BDNF, NGF, GAP43 CHRM1 2671/4885AKR1A1 2042/4885CHRM3 2784/4885
US-20160332940-A1 PROCESSES FOR THE SYNTHESIS OF CHIRAL 1-ALKANOLS CYP51A1, ALKBH3, ALKBH1 CHRM1 815/4885AKR1A1 134/4885CHRM3 1892/4885
US-20020028947-A1 Novel intermediates and processes for the preparation of optically active octanoic acid derivatives PDE6H, PDE6C, PDE6D CHRM1 1065/4885AKR1A1 391/4885CHRM3 280/4885
US-10000432-B2 Processes for the synthesis of chiral 1-alkanols CYP51A1, ALKBH3, ALKBH1 CHRM1 815/4885AKR1A1 134/4885CHRM3 1892/4885
US-20060135802-A1 Process for producing (2r)-2-propyloctanoic acid and intermediate therefor CYP51A1, POR, GRHPR CHRM1 2724/4885AKR1A1 61/4885CHRM3 2658/4885

“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.