SCHEMBL1097707

SCHEMBL1097707

CCOC(=O)c1cccc(N)c1C(=O)O

nearest known ligand 0.68

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 9/20 0.68
HSD17B10 Q99714 7/20 0.68
TSHR P16473 2/20 0.58
CDC25B P30305 4/20 0.53
HPGD P15428 6/20 0.50
RAB9A P51151 5/20 0.50
SMN1; SMN2 Q16637 5/20 0.50
MAPT P10636 3/20 0.50
GAA P10253 1/20 0.50
ALOX15 P16050 1/20 0.50
CA12 O43570 1/20 0.50
CA1 P00915 1/20 0.50
CA2 P00918 1/20 0.50
CA7 P43166 1/20 0.50
CA9 Q16790 1/20 0.50
CA14 Q9ULX7 1/20 0.50
NPC1 O15118 4/20 0.47
KDM4E B2RXH2 3/20 0.47
KMT2A Q03164 3/20 0.47
MEN1 O00255 2/20 0.47

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
SCHEMBL2894636 0.90 ALDH1A1 (0.72) ALDH1A1HSD17B10TSHRCDC25BHPGD
SCHEMBL11521675 0.88 TSHR (0.68) ALDH1A1HSD17B10TSHRCDC25BHPGD
SCHEMBL10353071 0.85 TSHR (0.63) ALDH1A1HSD17B10TSHRCDC25BHPGD
SCHEMBL7126414 0.84 ALDH1A1 (0.60) ALDH1A1HSD17B10TSHRCDC25BHPGD
SCHEMBL7617766 0.83 ALDH1A1 (0.58) ALDH1A1HSD17B10TSHRCDC25BHPGD
SCHEMBL1424504 0.83 TSHR (0.61) ALDH1A1HSD17B10TSHRCDC25BHPGD
Ethyl Anthranilate SCHEMBL7560547 0.83 ALDH1A1 (0.96) ALDH1A1HSD17B10TSHRCDC25BHPGD
Ethyl Anthranilate SCHEMBL27460908 0.82 ALDH1A1 (0.87) ALDH1A1HSD17B10TSHRCDC25BHPGD
SCHEMBL1097855 0.82 CA12 (0.71) ALDH1A1HSD17B10TSHRCDC25BRAB9A
SCHEMBL30216752 0.81 ALDH1A1 (0.65) ALDH1A1HSD17B10TSHRHPGDMAPT

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-109970568-B Synthesis process of 3-amino dimethyl phthalate 扬州工业职业技术学院 2022-09-02 CN claimed
CN-216172207-U Hydrogenation reaction kettle for preparing 3-amino-dimethyl phthalate 山东友帮生化科技有限公司 2022-04-05 CN claimed
CN-110483304-A A kind of preparation method of 3- aminophthalic acid dimethyl ester YANGZHOU POLYTECHNIC INST 2019-11-22 CN claimed
CN-109970568-A A kind of green synthesis process of 3- aminophthalic acid dimethyl ester 扬州工业职业技术学院 2019-07-05 CN claimed
CN-104945406-A Aza-phenalene-3-ketone derivative, preparation method thereof and application of aza-phenalene-3-ketone derivative as PARP inhibitor SUZHOU KANGRUN PHARMACEUTICALS INC 2015-09-30 CN claimed
CN-109970568-B Synthesis process of 3-amino dimethyl phthalate 扬州工业职业技术学院 2022-09-02 CN disclosed
CN-109970568-B Synthesis process of 3-amino dimethyl phthalate 扬州工业职业技术学院 2022-09-02 CN disclosed
CN-110746400-A Androgen receptor targeted fluorescent probe and preparation method thereof 郑州大学 2020-02-04 CN disclosed
CN-110483304-A A kind of preparation method of 3- aminophthalic acid dimethyl ester YANGZHOU POLYTECHNIC INST 2019-11-22 CN disclosed
CN-110483304-A A kind of preparation method of 3- aminophthalic acid dimethyl ester YANGZHOU POLYTECHNIC INST 2019-11-22 CN disclosed
CN-110483304-A A kind of preparation method of 3- aminophthalic acid dimethyl ester YANGZHOU POLYTECHNIC INST 2019-11-22 CN disclosed
US-10385037-B2 4′-O-substituted isoindoline derivatives and compositions comprising and methods of using the same CELGENE CORPORATION (US) 2019-08-20 US disclosed
US-20060025597-A1 Isoindole-imide compounds, compositions, and uses thereof CELGENE CORPORATION 2006-02-02 US disclosed
US-20060025457-A1 Isoindoline compounds and methods of their use AMGEN INC. 2006-02-02 US disclosed
EP-1363900-A1 ISOINDOLE-IMIDE COMPOUNDS AS TNF-INHIBITORS CELGENE CORPORATION (US) 2003-11-26 EP disclosed
US-20030096841-A1 Isoindole-imide compounds, compositions, and uses thereof CELGENE CORPORATION 2003-05-22 US disclosed
US-20030045552-A1 Isoindole-imide compounds, compositions, and uses thereof CELGENE CORPORATION 2003-03-06 US disclosed
WO-2002059106-A1 ISOINDOLE-IMIDE COMPOUNDS, COMPOSITIONS, AND USES THEREOF CELGENE CORPORATION (US) 2002-08-01 WO disclosed
EP-0781767-B1 Process for producing isatoic anhydrides SUMITOMO CHEMICAL CO (JP) 2001-09-05 EP disclosed
EP-0781767-A1 Process for producing isatoic anhydrides SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 1997-07-02 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-20030045552-A1 Isoindole-imide compounds, compositions, and uses thereof TNF, IKZF3, IKZF1 ALDH1A1 2514/4885HSD17B10 3247/4885TSHR 1322/4885
US-20060025597-A1 Isoindole-imide compounds, compositions, and uses thereof TNF, IKZF3, TNFRSF1A ALDH1A1 2190/4885HSD17B10 3313/4885TSHR 1341/4885
US-20030096841-A1 Isoindole-imide compounds, compositions, and uses thereof TNF, IKZF3, IKZF1 ALDH1A1 2514/4885HSD17B10 3247/4885TSHR 1322/4885
US-20060025457-A1 Isoindoline compounds and methods of their use PDE4A, PDE4B, PDE4C ALDH1A1 293/4885HSD17B10 723/4885TSHR 4195/4885
US-10385037-B2 4′-O-substituted isoindoline derivatives and compositions comprising and methods of using the same CYP3A4, CYP3A7, CYP4B1 ALDH1A1 1450/4885HSD17B10 1570/4885TSHR 4235/4885

“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.