Potassium

Potassium

SCHEMBL834916

Cc1nnc(C(=O)O)o1.[K]

nearest known ligand 0.42

Full drug profile on Sugi Atlas →

Predicted protein targets (top 15)

geneUniProtsupporting neighboursconfidence
PTPN1 P18031 1/20 0.41
HSD17B10 Q99714 1/20 0.34
ALDH1A1 P00352 3/20 0.31
KDM4E B2RXH2 2/20 0.31
LMNA P02545 2/20 0.31
HPGD P15428 1/20 0.31
TDP1 Q9NUW8 1/20 0.31
DPP4 P27487 1/20 0.31
DPP8 Q6V1X1 1/20 0.31
DPP7 Q9UHL4 1/20 0.31
CTSA P10619 1/20 0.30
MITF O75030 1/20 0.30
MAPT P10636 1/20 0.30
HCAR2 Q8TDS4 1/20 0.30
EPHX2 P34913 1/20 0.30

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
SCHEMBL185561 0.98
SCHEMBL22436525 0.95 PTPN1 (0.41) PTPN1HSD17B10ALDH1A1KDM4ELMNA
Hydrochloric Acid SCHEMBL22436543 0.95 PTPN1 (0.41) PTPN1HSD17B10ALDH1A1KDM4ELMNA
SCHEMBL13302546 0.82
SCHEMBL13275068 0.80 KDM4E (0.38) HSD17B10ALDH1A1KDM4ELMNAHPGD
SCHEMBL17040253 0.79 PTPN1 (0.50) PTPN1ALDH1A1
Hydrochloric Acid SCHEMBL11596232 0.76 PTPN1 (0.48) PTPN1ALDH1A1
SCHEMBL3355222 0.76
SCHEMBL52596 0.76
Hydrochloric Acid SCHEMBL3327764 0.74 EPHX2 (0.33) HSD17B10ALDH1A1KDM4ELMNAHPGD

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 16 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-117715909-A Condensed heterocyclic derivative 杨森科学爱尔兰无限公司 2024-03-15 CN disclosed
CN-113272309-B Tricyclic inhibitors of hepatitis b virus 圣拉斐尔医院有限公司 2024-02-23 CN disclosed
US-11246869-B2 Process for the preparation of Raltegravir CAMBREX PROFARMACO MILANO S.R.L. (IT) 2022-02-15 US disclosed
US-20200330466-A1 PROCESS FOR THE PREPARATION OF RALTEGRAVIR CAMBREX PROFARMACO MILANO S.R.L. (IT) 2020-10-22 US disclosed
EP-3710445-A1 PROCESS FOR THE PREPARATION OF RALTEGRAVIR Cambrex Profarmaco Milano S.r.l. (IT) 2020-09-23 EP disclosed
US-20120252770-A1 Chemical Compounds 572 BAYER PHARMA AKTIENGESELLSCHAFT (DE) 2012-10-04 US disclosed
CN-101611015-B Indazolyl ester and indazolyl amide derivatives for the treatment of glucocorticoid receptor mediated disorders ASTRAZENECA AB SE 2012-09-26 CN disclosed
EP-2102169-B1 INDAZOLYL AMIDE DERIVATIVES FOR THE TREATMENT OF GLUCOCORTICOID RECEPTOR MEDIATED DISORDERS ASTRAZENECA AB (SE) 2012-06-20 EP disclosed
US-8143290-B2 Chemical compounds 572 ASTRAZENECA AB (SE) 2012-03-27 US disclosed
US-20110071194-A1 Chemical Compounds 572 BAYER PHARMA AKTIENGESELLSCHAFT (DE) 2011-03-24 US disclosed
US-20100197644-A1 Chemical Compounds 572 BAYER PHARMA AKTIENGESELLSCHAFT (DE) 2010-08-05 US disclosed
US-7728030-B2 Chemical compounds 572 ASTRAZENECA AB (SE) 2010-06-01 US disclosed
CN-101611015-A Indazolyl ester and indazolyl amide derivatives for the treatment of glucocorticoid receptor mediated disorders ASTRAZENECA AB (SE) 2009-12-23 CN disclosed
EP-2102169-A1 INDAZOLYL ESTER AND AMIDE DERIVATIVES FOR THE TREATMENT OF GLUCOCORTICOID RECEPTOR MEDIATED DISORDERS AstraZeneca AB (SE) 2009-09-23 EP disclosed
US-20080214641-A1 Chemical compounds 572 BAYER PHARMA AKTIENGESELLSCHAFT (DE) 2008-09-04 US disclosed
WO-2008076048-A1 INDAZOLYL ESTER AND AMIDE DERIVATIVES FOR THE TREATMENT OF GLUCOCORTICOID RECEPTOR MEDIATED DISORDERS ASTRAZENECA AB (SE) 2008-06-26 WO 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 (6 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-20080214641-A1 Chemical compounds 572 ABCG2, ABCB1, CYP11B2 PTPN1 4815/4885HSD17B10 1784/4885ALDH1A1 699/4885
US-20100197644-A1 Chemical Compounds 572 ABCG2, ABCB1, CYP11B2 PTPN1 4815/4885HSD17B10 1784/4885ALDH1A1 699/4885
US-20120252770-A1 Chemical Compounds 572 ABCG2, ABCB1, CYP11B2 PTPN1 4815/4885HSD17B10 1784/4885ALDH1A1 699/4885
US-20200330466-A1 PROCESS FOR THE PREPARATION OF RALTEGRAVIR SAMHD1, CYP3A4, UGT1A4 PTPN1 4160/4885HSD17B10 1519/4885ALDH1A1 254/4885
US-11246869-B2 Process for the preparation of Raltegravir SAMHD1, CYP3A4, UGT1A4 PTPN1 4160/4885HSD17B10 1519/4885ALDH1A1 254/4885
US-20110071194-A1 Chemical Compounds 572 ABCG2, ABCB1, CYP11B2 PTPN1 4815/4885HSD17B10 1784/4885ALDH1A1 699/4885

“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.