SCHEMBL2073499

SCHEMBL2073499

OCCc1csc(-c2ccc(Cl)cc2)n1

nearest known ligand 0.68

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
GFER P55789 1/20 0.68
TP53 P04637 8/20 0.54
LMNA P02545 6/20 0.54
MAPT P10636 7/20 0.54
RAB9A P51151 2/20 0.51
MEN1 O00255 1/20 0.51
NPC1 O15118 1/20 0.51
ALDH1A1 P00352 1/20 0.51
CYP1A2 P05177 1/20 0.51
CYP3A4 P08684 1/20 0.51
CYP2D6 P10635 1/20 0.51
CYP2C9 P11712 1/20 0.51
CYP2C19 P33261 1/20 0.51
KMT2A Q03164 1/20 0.51
HIF1A Q16665 1/20 0.51
HSD17B10 Q99714 1/20 0.51
POLB P06746 1/20 0.51
THRB P10828 1/20 0.49
KDM4E B2RXH2 1/20 0.49
SMN1; SMN2 Q16637 1/20 0.49

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
SCHEMBL1177423 0.86 GFER (0.72) GFERTP53LMNAMAPTRAB9A
SCHEMBL4284871 0.85 GFER (0.75) GFERTP53LMNAMAPTRAB9A
SCHEMBL28003279 0.83 GFER (0.68) GFERTP53LMNAMAPTRAB9A
SCHEMBL2224601 0.83 GFER (0.68) GFERTP53LMNAMAPTRAB9A
SCHEMBL4902662 0.83 LMNA (0.63) TP53LMNAMAPTALDH1A1POLB
SCHEMBL3369620 0.83 LMNA (0.57) GFERTP53LMNAMAPTRAB9A
SCHEMBL13064774 0.83 GFER (0.68) GFERTP53LMNAMAPTRAB9A
SCHEMBL3371889 0.83 LMNA (0.56) LMNAMAPTRAB9AALDH1A1HSD17B10
SCHEMBL3372943 0.83 GFER (0.46) GFERTP53LMNAMAPTRAB9A
SCHEMBL4904228 0.82 TP53 (0.49) GFERTP53LMNAMAPTPOLB

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20210275502-A1 PROCESS FOR PREPARING A POTENT THIAZOLE COMPOUND, PHARMACEUTICAL FORMULATION AND USES THEREOF AHAMMUNE BIOSCIENCES PRIVATE LIMITED (IN) 2021-09-09 US claimed
US-20260034104-A1 PROCESS FOR PREPARING A POTENT THIAZOLE COMPOUND, PHARMACEUTICAL FORMULATION AND USES THEREOF AHAMMUNE BIOSCIENCES PRIVATE LTD (IN) 2026-02-05 US disclosed
US-12440478-B2 Process for preparing a potent thiazole compound, pharmaceutical formulation and uses thereof AHAMMUNE BIOSCIENCES PRIVATE LIMITED (IN) 2025-10-14 US disclosed
US-20210275502-A1 PROCESS FOR PREPARING A POTENT THIAZOLE COMPOUND, PHARMACEUTICAL FORMULATION AND USES THEREOF AHAMMUNE BIOSCIENCES PRIVATE LIMITED (IN) 2021-09-09 US disclosed
US-20210275502-A1 PROCESS FOR PREPARING A POTENT THIAZOLE COMPOUND, PHARMACEUTICAL FORMULATION AND USES THEREOF AHAMMUNE BIOSCIENCES PRIVATE LIMITED (IN) 2021-09-09 US disclosed
EP-2089397-B1 5- [4- (AZETIDIN-3-YL0XY) -PHENYL]-2-PHENYL-5H-THIAZ0L0 [5,4-C]PYRIDIN-4-0NE DERIVATIVES AND THEIR USE AS MCH RECEPTOR ANTAGONISTS LILLY CO ELI (US) 2012-08-29 EP disclosed
CN-101080411-B Thiazolopyridinone derivatives as MCH receptor antagonists LILLY CO ELI 2011-11-02 CN disclosed
US-8049013-B2 5- [4-(azetidin-3-yloxy)-phenyl]-2-phenyl-5H-thiazolo[5,4-C] pyridin-4-one derivatives and their use as MCH receptor antagonists ELI LILLY AND COMPANY (US) 2011-11-01 US disclosed
US-7902356-B2 Thiazolopyridinone derivates as MCH receptor antagonists ELI LILLY AND COMPANY (US) 2011-03-08 US disclosed
US-7902356-B2 Thiazolopyridinone derivates as MCH receptor antagonists ELI LILLY AND COMPANY (US) 2011-03-08 US disclosed
CN-101558075-A 5- [4- (azetidin-3-yl0xy) -phenyl] -2-phenyl-5h-thiaz0l0 [5,4-c] pyridin-4-0ne derivatives and their use as mch receptor antagonists LILLY CO ELI (US) 2009-10-14 CN disclosed
US-20090233919-A1 THIAZOLOPYRIDINONE DERIVATES AS MCH RECEPTOR ANTAGONISTS ELI LILLY AND COMPANY 2009-09-17 US disclosed
US-20090233919-A1 THIAZOLOPYRIDINONE DERIVATES AS MCH RECEPTOR ANTAGONISTS ELI LILLY AND COMPANY 2009-09-17 US disclosed
US-20090233919-A1 THIAZOLOPYRIDINONE DERIVATES AS MCH RECEPTOR ANTAGONISTS ELI LILLY AND COMPANY 2009-09-17 US disclosed
EP-2089397-A1 5- [4- (AZETIDIN-3-YL0XY) -PHENYL]-2-PHENYL-5H-THIAZ0L0 [5,4-C]PYRIDIN-4-0NE DERIVATIVES AND THEIR USE AS MCH RECEPTOR ANTAGONISTS Eli Lilly & Company (US) 2009-08-19 EP disclosed
WO-2008076562-A1 5- [4- (AZETIDIN-3-YL0XY) -PHENYL] -2-PHENYL-5H-THIAZ0L0 [5,4-C] PYRIDIN-4-0NE DERIVATIVES AND THEIR USE AS MCH RECEPTOR ANTAGONISTS ELI LILLY AND COMPANY (US) 2008-06-26 WO disclosed
CN-101080411-A Thiazolopyridinone derivatives as MCH receptor antagonists LILLY CO ELI (US) 2007-11-28 CN disclosed
EP-1828207-A1 THIAZOLOPYRIDINONE DERIVATES AS MCH RECEPTOR ANTAGONISTS ELI LILLY AND COMPANY (US) 2007-09-05 EP disclosed
WO-2006066174-A1 THIAZOLOPYRIDINONE DERIVATES AS MCH RECEPTOR ANTAGONISTS ELI LILLY AND COMPANY (US) 2006-06-22 WO disclosed
US-4033977-A ANTIINFLAMMATORY, ANTIDEPRESSANT AMERICAN HOME PRODUCTS CORPORATION (US) 1977-07-05 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 (4 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-12440478-B2 Process for preparing a potent thiazole compound, pharmaceutical formulation and uses thereof TYR, MITF, TPP2 GFER 3206/4885TP53 3240/4885LMNA 2729/4885
US-20210275502-A1 PROCESS FOR PREPARING A POTENT THIAZOLE COMPOUND, PHARMACEUTICAL FORMULATION AND USES THEREOF TYR, MITF, TPP2 GFER 3206/4885TP53 3240/4885LMNA 2729/4885
US-20260034104-A1 PROCESS FOR PREPARING A POTENT THIAZOLE COMPOUND, PHARMACEUTICAL FORMULATION AND USES THEREOF SSB, MITF, HLA-DRB1 GFER 4530/4885TP53 1601/4885LMNA 553/4885
US-20090233919-A1 THIAZOLOPYRIDINONE DERIVATES AS MCH RECEPTOR ANTAGONISTS MCHR1, MCHR2, MC1R GFER 3668/4885TP53 3759/4885LMNA 3649/4885

“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.