SCHEMBL2092006

SCHEMBL2092006

[CH2]C(=O)c1cc(C)ccc1C

nearest known ligand 0.53

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
MEN1 O00255 2/20 0.53
KMT2A Q03164 2/20 0.53
CSNK2A1 P68400 1/20 0.47
TSHR P16473 1/20 0.46
SMN1; SMN2 Q16637 4/20 0.44
GAA P10253 1/20 0.42
HDAC3 O15379 1/20 0.42
HDAC4 P56524 1/20 0.42
HDAC1 Q13547 1/20 0.42
HDAC7 Q8WUI4 1/20 0.42
HDAC2 Q92769 1/20 0.42
HDAC10 Q969S8 1/20 0.42
HDAC11 Q96DB2 1/20 0.42
HDAC8 Q9BY41 1/20 0.42
HDAC6 Q9UBN7 1/20 0.42
HDAC9 Q9UKV0 1/20 0.42
HDAC5 Q9UQL6 1/20 0.42
HSD17B10 Q99714 1/20 0.41
ALDH1A1 P00352 1/20 0.41
NPC1 O15118 1/20 0.41

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
SCHEMBL2090993 0.82 NFE2L2 (0.47) MEN1KMT2ACSNK2A1SMN1; SMN2ALDH1A1
SCHEMBL9862051 0.81 MEN1 (0.57) MEN1KMT2ACSNK2A1TSHRSMN1; SMN2
SCHEMBL9420245 0.81 MEN1 (0.57) MEN1KMT2ACSNK2A1TSHRSMN1; SMN2
SCHEMBL29636568 0.79 KMT2A (0.55) MEN1KMT2ACSNK2A1TSHRSMN1; SMN2
SCHEMBL697905 0.79 KMT2A (0.55) MEN1KMT2ACSNK2A1TSHRSMN1; SMN2
SCHEMBL223101 0.79 CSNK2A1 (0.65) MEN1KMT2ACSNK2A1TSHRSMN1; SMN2
SCHEMBL501733 0.79 MEN1 (0.55) MEN1KMT2ACSNK2A1TSHRSMN1; SMN2
SCHEMBL10389402 0.78 MEN1 (0.50) MEN1KMT2ACSNK2A1TSHRSMN1; SMN2
SCHEMBL7113261 0.78 MEN1 (0.50) MEN1KMT2ACSNK2A1TSHRSMN1; SMN2
SCHEMBL18568450 0.78 MEN1 (0.53) MEN1KMT2ACSNK2A1TSHRSMN1; SMN2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-9714560-B2 Protected scale inhibitors and methods relating thereto HALLIBURTON ENERGY SERVICES, INC. (US) 2017-07-25 US claimed
CN-117986153-A Ionizable cationic lipid compound, and preparation method and application thereof 晟迪生物医药(苏州)有限公司 2024-05-07 CN disclosed
US-20220153932-A1 PREPOLYMERS OF 1,1-DICARBONYL SUBSTITUTED-1-ALKENE, METHODS TO MAKE THEM, POLYMERS MADE FROM THEM AND METHODS TO MAKE THE POLYMER SIRRUS INC (US) 2022-05-19 US disclosed
US-20220112151-A1 COMPOSITIONS OF DICARBONYL SUBSTITUTED-1-ALKENE, METHODS TO MAKE THEM, POLYMERS MADE FROM THEM AND METHODS TO MAKE THE POLYMER SIRRUS INC (US) 2022-04-14 US disclosed
US-11198757-B2 Compositions including a photolatent amine, camphorquinone, and coumarin and related methods 3M INNOVATIVE PROPERTIES COMPANY (US) 2021-12-14 US disclosed
US-20210371667-A1 COMPOSITION INCLUDING AMINO-FUNCTIONAL SILANES AND METHOD OF APPLYING A SEALANT TO A SUBSTRATE 3M INNOVATIVE PROPERTIES COMPANY 2021-12-02 US disclosed
WO-2021231288-A1 IMPROVED DICARBONYL SUBSTITUTED-1-ALKENE COMPOSITIONS NIPPON SHOKUBAI CO., LTD. (JP) 2021-11-18 WO disclosed
US-11090681-B2 Composition including a polythiol, a polyepoxide, a photolatent base, and an amine and methods relating to the composition 3M INNOVATIVE PROPERTIES COMPANY (US) 2021-08-17 US disclosed
EP-3856849-A1 COMPOSITION INCLUDING AMINO-FUNCTIONAL SILANES AND METHOD OF APPLYING A SEALANT TO A SUBSTRATE 3M Innovative Properties Company (US) 2021-08-04 EP disclosed
WO-2021150844-A1 COMPOSITIONS CONTAINING 1,1-DISUBSTITUTED ACTIVATED ALKENES USEFUL IN ADDITIVE MANUFACTURING AND ARTICLES FORMED THEREFROM SIRRUS, INC. (US) 2021-07-29 WO disclosed
EP-2570418-A2 2,3-dihydro-6-nitroimidazo[2,1-b]oxazoles compound OTSUKA PHARMACEUTICAL CO., LTD. (JP) 2013-03-20 EP disclosed
EP-1555267-B1 2,3-DIHYDRO-6-NITROIMIDAZO[2,1-b]OXAZOLES OTSUKA PHARMA CO LTD (JP) 2013-01-16 EP disclosed
US-8163753-B2 2-(4-(4-(4-chlorophenyl)oxazol-2-yl)phenoxymethyl)-2-methyl-6-nitro-2,3-dihydroimidazo[2,1-b]oxazole; bactericide; excellent bactericidal action against Mycobacterium tuberculosis, multi-drug-resistant Mycobacterium tuberculosis, and atypical acid-fast bacteria OTSUKA PHARMACEUTICAL CO., LTD. (JP) 2012-04-24 US disclosed
EP-1678185-B1 2,3-DIHYDRO-6-NITROIMIDAZO [2,1-B] OXAZOLE COMPOUNDS FOR THE TREATMENT OF TUBERCULOSIS OTSUKA PHARMA CO LTD (JP) 2008-10-08 EP disclosed
US-20080119478-A1 2,3-Dihydro-6-Nitroimidazo (2,1-b) Oxazole Compounds for the Treatment of Tuberculosis OTSUKA PHAMACEUTICAL CO., LTD. (JP) 2008-05-22 US disclosed
US-7262212-B2 2,3-dihydro-6-nitroimidazo[2,1-b]oxazoles OTSUKA PHARMACEUTICAL CO., LTD. (JP) 2007-08-28 US disclosed
EP-1678185-A1 2,3-DIHYDRO-6-NITROIMIDAZO [2,1-B] OXAZOLE COMPOUNDS FOR THE TREATMENT OF TUBERCULOSIS OTSUKA PHARMACEUTICAL CO., LTD. (JP) 2006-07-12 EP disclosed
US-20060094767-A1 2,3-Dihydro-6-nitroimidazo[2,1-b]oxazoles OTSUKA PHARMACEUTICAL CO., LTD. (JP) 2006-05-04 US disclosed
EP-1555267-A1 2,3-DIHYDRO-6-NITROIMIDAZO 2,1-b OXAZOLES OTSUKA PHARMACEUTICAL CO., LTD. (JP) 2005-07-20 EP disclosed
WO-2005042542-A1 2,3-DIHYDRO-6-NITROIMIDAZO (2,1-B) OXAZOLE COMPOUNDS FOR THE TREATMENT OF TUBERCULOSIS OTSUKA PHARMACEUTICAL CO., LTD. (JP) 2005-05-12 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 (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-20060094767-A1 2,3-Dihydro-6-nitroimidazo[2,1-b]oxazoles NR2C2, NR4A3, NR4A2 MEN1 3295/4885KMT2A 4267/4885CSNK2A1 1171/4885
US-20220112151-A1 COMPOSITIONS OF DICARBONYL SUBSTITUTED-1-ALKENE, METHODS TO MAKE THEM, POLYMERS MADE FROM THEM AND METHODS TO MAKE THE POLYMER PARG, PARN, LIG1 MEN1 1628/4885KMT2A 2305/4885CSNK2A1 3915/4885
US-20080119478-A1 2,3-Dihydro-6-Nitroimidazo (2,1-b) Oxazole Compounds for the Treatment of Tuberculosis NR2C2, NR0B2, NR4A2 MEN1 4525/4885KMT2A 3324/4885CSNK2A1 967/4885
US-20220153932-A1 PREPOLYMERS OF 1,1-DICARBONYL SUBSTITUTED-1-ALKENE, METHODS TO MAKE THEM, POLYMERS MADE FROM THEM AND METHODS TO MAKE THE POLYMER PLOD1, COL1A1, PLOD2 MEN1 1555/4885KMT2A 2902/4885CSNK2A1 4400/4885

“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.