SCHEMBL3389649

SCHEMBL3389649

COC(=O)CC(C)C(C(=O)OC)C(=O)OC

nearest known ligand 0.48

Predicted protein targets (top 19)

geneUniProtsupporting neighboursconfidence
SMN1; SMN2 Q16637 2/20 0.48
TSHR P16473 5/20 0.40
MGAM O43451 2/20 0.37
GAA P10253 2/20 0.37
SI P14410 2/20 0.37
MGAM2 Q2M2H8 2/20 0.37
HSD17B10 Q99714 1/20 0.37
CA14 Q9ULX7 3/20 0.35
KCNA5 P22460 1/20 0.35
MAPT P10636 1/20 0.34
RAB9A P51151 1/20 0.34
CA12 O43570 2/20 0.33
KMT2A Q03164 3/20 0.33
MEN1 O00255 2/20 0.33
CA1 P00915 1/20 0.32
CA2 P00918 1/20 0.32
CA7 P43166 1/20 0.32
CA9 Q16790 1/20 0.32
TET2 Q6N021 1/20 0.31

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
SCHEMBL3389644 1.00 SMN1; SMN2 (0.48) SMN1; SMN2TSHRMGAMGAASI
SCHEMBL3396195 0.85 MGAM (0.43) SMN1; SMN2TSHRMGAMGAASI
SCHEMBL3397834 0.85 MGAM (0.43) SMN1; SMN2TSHRMGAMGAASI
SCHEMBL3397234 0.85 GAA (0.48) SMN1; SMN2TSHRMGAMGAASI
SCHEMBL3394662 0.85 GAA (0.48) SMN1; SMN2TSHRMGAMGAASI
SCHEMBL5081302 0.83 TSHR (0.50) SMN1; SMN2TSHRMGAMGAASI
SCHEMBL5077875 0.83 TSHR (0.50) SMN1; SMN2TSHRMGAMGAASI
SCHEMBL16626900 0.82 SMN1; SMN2 (0.41) SMN1; SMN2HSD17B10MAPTCA1CA2
SCHEMBL3396358 0.82 TSHR (0.33) SMN1; SMN2TSHRMGAMGAASI
SCHEMBL3396035 0.82 TSHR (0.33) SMN1; SMN2TSHRMGAMGAASI

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-8969051-B2 Process for producing optically active 2-alkyl-1,1,3-trialkoxycarbonylpropane SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2015-03-03 US claimed
US-12617784-B2 AKT inhibitor NANJING CHIA TAI TIANQING PHARMACEUTICAL CO., LTD. (CN) 2026-05-05 US disclosed
EP-3919491-B1 AKT INHIBITOR NANJING CHIA TAI TIANQING PHARMACEUTICAL CO LTD (CN) 2025-05-28 EP disclosed
US-20230321108-A1 UNIT DOSAGE COMPOSITION OF AKT INHIBITOR NANJING CHIA TAI TIANQING PHARMACEUTICAL CO., LTD. (CN) 2023-10-12 US 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-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
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
US-9309204-B2 Process for making hydroxylated cyclopentylpyrimidine compounds ARRAY BIOPHARMA INC. (US) 2016-04-12 US disclosed
US-9309204-B2 Process for making hydroxylated cyclopentylpyrimidine compounds ARRAY BIOPHARMA INC. (US) 2016-04-12 US disclosed
US-20150218602-A1 PROCESS FOR PRODUCING OPTICALLY ACTIVE 2-ALKYL-1,1,3-TRIALKOXYCARBONYLPROPANE GENENTECH INC (US) 2015-08-06 US disclosed
EP-2861583-A1 PROCESS FOR MAKING HYDROXYLATED CYCLOPENTYLPYRIMIDINE COMPOUNDS Array Biopharma, Inc. (US) 2015-04-22 EP disclosed
US-20150099881-A1 PROCESS FOR MAKING HYDROXYLATED CYCLOPENTYLPYRIMIDINE COMPOUNDS GENETECH, INC. (US) 2015-04-09 US disclosed
US-20150099881-A1 PROCESS FOR MAKING HYDROXYLATED CYCLOPENTYLPYRIMIDINE COMPOUNDS GENETECH, INC. (US) 2015-04-09 US disclosed
US-8969051-B2 Process for producing optically active 2-alkyl-1,1,3-trialkoxycarbonylpropane SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2015-03-03 US disclosed
WO-2013173736-A1 PROCESS FOR MAKING HYDROXYLATED CYCLOPENTYLPYRIMIDINE COMPOUNDS ARRAY BIOPHARMA INC. (US) 2013-11-21 WO disclosed
US-20100240107-A1 PROCESS FOR PRODUCING OPTICALLY ACTIVE 2-ALKYL-1,1,3-TRIALKOXYCARBONYLPROPANE SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2010-09-23 US disclosed
EP-2154253-A1 PROCESS FOR PRODUCING OPTICALLY ACTIVE 2-ALKYL-1,1,3-TRIALKOXYCARBONYLPROPANE Sumitomo Chemical Company, Limited (JP) 2010-02-17 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-20150099881-A1 PROCESS FOR MAKING HYDROXYLATED CYCLOPENTYLPYRIMIDINE COMPOUNDS PIK3CA, DHPS, PIK3CD SMN1; SMN2 3946/4885TSHR 3644/4885MGAM 4227/4885
US-12617784-B2 AKT inhibitor AKT2, AKT1, AKT3 SMN1; SMN2 1551/4885TSHR 900/4885MGAM 4031/4885
US-20230321108-A1 UNIT DOSAGE COMPOSITION OF AKT INHIBITOR AKT2, AKT1, PIK3R2 SMN1; SMN2 2468/4885TSHR 3863/4885MGAM 1820/4885
US-20230286979-A1 SALT OF DIHYDROPYRIDO[2,3-D]PYRIMIDINONE DERIVATIVE, PREPARATION METHOD THEREFOR, AND USE THEREOF FH, GRHPR, SDHB SMN1; SMN2 4120/4885TSHR 4842/4885MGAM 1406/4885
US-20230271958-A1 SALT AND CRYSTAL FORM OF DIHYDROPYRIDO[2,3-d]PYRIMIDINE DERIVATE DCK, DPYD, UCK2 SMN1; SMN2 3624/4885TSHR 3509/4885MGAM 3247/4885

“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.