SCHEMBL66573

SCHEMBL66573

CCC[C@@H](C(=O)O)N(C)C(=O)OC(C)(C)C

nearest known ligand 0.41

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
HDAC1 Q13547 2/20 0.41
HDAC2 Q92769 2/20 0.41
CHRM1 P11229 1/20 0.41
AKR1A1 P14550 1/20 0.41
CHRM3 P20309 1/20 0.41
HTR2A P28223 1/20 0.41
HTR2C P28335 1/20 0.41
ADRA1A P35348 1/20 0.41
HRH1 P35367 1/20 0.41
DRD3 P35462 1/20 0.41
SLC6A3 Q01959 1/20 0.41
TDP1 Q9NUW8 1/20 0.41
MMP13 P45452 1/20 0.38
SLC1A2 P43004 3/20 0.37
SLC1A1 P43005 3/20 0.37
SLC1A3 P43003 2/20 0.37
GRIK1 P39086 2/20 0.37
GRIK2 Q13002 2/20 0.37
CA2 P00918 2/20 0.36
CA12 O43570 2/20 0.36

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
SCHEMBL20826464 1.00 HDAC1 (0.41) HDAC1HDAC2CHRM1AKR1A1CHRM3
SCHEMBL67491 1.00 HDAC1 (0.41) HDAC1HDAC2CHRM1AKR1A1CHRM3
SCHEMBL66398 0.90 CA2 (0.42) MMP13SLC1A2SLC1A1SLC1A3GRIK1
SCHEMBL66399 0.90 CA2 (0.42) MMP13SLC1A2SLC1A1SLC1A3GRIK1
SCHEMBL29696200 0.90 CA2 (0.42) MMP13SLC1A2SLC1A1SLC1A3GRIK1
SCHEMBL31407436 0.89 GRIK1 (0.41) MMP13SLC1A2SLC1A1SLC1A3GRIK1
SCHEMBL8460619 0.89 GRIK1 (0.41) MMP13SLC1A2SLC1A1SLC1A3GRIK1
SCHEMBL25177958 0.87 GRIK1 (0.43) SLC1A2SLC1A1GRIK1GRIK2CA2
SCHEMBL27041525 0.87 MEN1 (0.37) HDAC1HDAC2TDP1MMP13CA14
SCHEMBL27041531 0.87 MEN1 (0.37) HDAC1HDAC2TDP1MMP13CA14

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20260015313-A1 AMINO ACID ACTIVE ESTER AND SALT THEREOF PEPTIDREAM INC (JP) 2026-01-15 US disclosed
US-20250281433-A1 NOVEL DERIVATIVE COMPOUND HAVING BIPHENYL GROUP INTRODUCED INTO AMINO-ALKANOIC ACID AND ANTI-INFLAMMATORY COMPOSITION COMPRISING SAME AMTIXBIO CO., LTD. (KR) 2025-09-11 US disclosed
US-12286455-B2 Anthelmintic depsipeptide compounds Boehringer Ingelheim Animal Health USA Inc. (US) 2025-04-29 US disclosed
EP-4534524-A1 AMINO ACID ACTIVE ESTER AND SALT THEREOF PeptiDream Inc. (JP) 2025-04-09 EP disclosed
US-12180139-B2 Method for preparing aminoalkanoic acid derivative containing biphenyl group AMTIXBIO CO., LTD. (KR) 2024-12-31 US disclosed
US-12172945-B2 Aminoalkanoic acid derivative containing biphenyl group and use of the same AMTIXBIO CO., LTD. (KR) 2024-12-24 US disclosed
US-12129220-B2 Pharmaceutical composition comprising aminoalkanoic acid derivative containing biphenyl group AMTIXBIO CO., LTD. (KR) 2024-10-29 US disclosed
EP-3992177-B1 DERIVATIVE COMPOUND INTRODUCING BIPHENYL GROUP INTO NOVEL AMINOALKANOIC ACID AND ANTIFUNGAL PHARMACEUTICAL COMPOSITION COMPRISING SAME AMTIXBIO CO LTD (KR) 2024-05-08 EP disclosed
EP-4268811-A1 NOVEL DERIVATIVE COMPOUND HAVING BIPHENYL GROUP INTRODUCED INTO AMINO-ALKANOIC ACID AND ANTI-INFLAMMATORY COMPOSITION COMPRISING SAME Amtixbio Co., Ltd. (KR) 2023-11-01 EP disclosed
CN-116887821-A Derivative compound for introducing biphenyl into novel amino alkanoic acid and anti-inflammatory composition containing the same 阿米蒂比奥有限公司 2023-10-13 CN disclosed
US-20170022253-A1 ANTHELMINTIC DEPSIPEPTIDE COMPOUNDS MERIAL INC. (US) 2017-01-26 US disclosed
WO-2016187534-A1 ANTHELMINTIC DEPSIPEPTIDE COMPOUNDS MERIAL, INC. (US) 2016-11-24 WO disclosed
WO-2016187534-A1 ANTHELMINTIC DEPSIPEPTIDE COMPOUNDS MERIAL, INC. (US) 2016-11-24 WO disclosed
US-8129417-B2 Substituted octahydrocyclopenta[C]pyrrol-4-amines as calcium channel blockers ABBOTT LABORATORIES (US) 2012-03-06 US disclosed
CN-102292319-A Novel substituted octahydrocyclopenta(C)pyrrol-4-amines as calcium channel blockers 2011-12-21 CN disclosed
WO-2011149995-A1 NOVEL SUBSTITUTED OCTAHYDROCYCLOPENTA [C]PYRROL-4-AMINES AS CALCIUM CHANNEL BLOCKERS ABBOTT LABORATORIES (US) 2011-12-01 WO disclosed
US-20110281870-A1 NOVEL SUBSTITUTED OCTAHYDROCYCLOPENTA[C]PYRROL-4-AMINES AS CALCIUM CHANNEL BLOCKERS ABBOTT LABORATORIES (US) 2011-11-17 US disclosed
EP-2367790-A2 SUBSTITUTED OCTAHYDROCYCLOPENTA(C)PYRROL-4-AMINES AS CALCIUM CHANNEL BLOCKERS Abbott Laboratories (US) 2011-09-28 EP disclosed
WO-2010062927-A2 NOVEL SUBSTITUTED OCTAHYDROCYCLOPENTA(C)PYRROL-4-AMINES AS CALCIUM CHANNEL BLOCKERS ABBOTT LABORATORIES (US) 2010-06-03 WO disclosed
US-20100130558-A1 NOVEL SUBSTITUTED OCTAHYDROCYCLOPENTA[C]PYRROL-4-AMINES AS CALCIUM CHANNEL BLOCKERS ABBOTT LABORATORIES (US) 2010-05-27 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 (9 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-12172945-B2 Aminoalkanoic acid derivative containing biphenyl group and use of the same GABBR1, AADAC, GABBR2 HDAC1 3391/4885HDAC2 1930/4885CHRM1 4577/4885
US-20170022253-A1 ANTHELMINTIC DEPSIPEPTIDE COMPOUNDS VIP, PREP, DNPEP HDAC1 279/4885HDAC2 668/4885CHRM1 2615/4885
US-20100130558-A1 NOVEL SUBSTITUTED OCTAHYDROCYCLOPENTA[C]PYRROL-4-AMINES AS CALCIUM CHANNEL BLOCKERS CACNA1C, ORAI1, CACNA1S HDAC1 1302/4885HDAC2 1891/4885CHRM1 92/4885
US-20260015313-A1 AMINO ACID ACTIVE ESTER AND SALT THEREOF NSUN3, BCAT1, SLC43A1 HDAC1 3148/4885HDAC2 3619/4885CHRM1 3968/4885
US-20110281870-A1 NOVEL SUBSTITUTED OCTAHYDROCYCLOPENTA[C]PYRROL-4-AMINES AS CALCIUM CHANNEL BLOCKERS CACNA1C, ORAI1, CACNA1S HDAC1 1302/4885HDAC2 1891/4885CHRM1 92/4885
US-12180139-B2 Method for preparing aminoalkanoic acid derivative containing biphenyl group AKR7A2, CYP51A1, APEH HDAC1 3684/4885HDAC2 2135/4885CHRM1 4547/4885
US-20250281433-A1 NOVEL DERIVATIVE COMPOUND HAVING BIPHENYL GROUP INTRODUCED INTO AMINO-ALKANOIC ACID AND ANTI-INFLAMMATORY COMPOSITION COMPRISING SAME AADAT, AADAC, AHR HDAC1 1365/4885HDAC2 960/4885CHRM1 3386/4885
US-12286455-B2 Anthelmintic depsipeptide compounds VIP, PREP, DNPEP HDAC1 279/4885HDAC2 668/4885CHRM1 2615/4885
US-12129220-B2 Pharmaceutical composition comprising aminoalkanoic acid derivative containing biphenyl group AHR, AADAC, GABBR1 HDAC1 3700/4885HDAC2 2093/4885CHRM1 4594/4885

“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.