Benzo[D]Thiazole

Benzo[D]Thiazole

SCHEMBL3765441

Cl.c1ccc2scnc2c1

nearest known ligand 0.95

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ABL1ACEACHEACVR1ADRA1AADRA1BADRA1DADRA2AADRA2BADRA2CADRB1ADRB2ADRB3AGTR1ALKAVPR1AAVPR2BCHEBCRCA2CACNA1ACACNA1BCACNA1CCACNA1DCACNA1ECACNA1FCACNA1GCACNA1HCACNA1ICACNA1SCACNA2D1CACNA2D2CACNA2D3CACNA2D4CACNB1CACNB2CACNB3CACNB4CACNG1CACNG2CACNG3CACNG4CACNG5CACNG6CACNG7CACNG8CALCRLCASRCCR5CDK4CDK6CFBCHRM1CHRM2CHRM3CHRM4CHRM5CHRNA1CHRNA3CHRNA7CHRNB1CHRNB4CHRNDCHRNECHRNGCOXFA4COXFA4L2CRBNCSF1RCUL4ACYP19A1DDB1DPP4DRD1DRD2DRD3DRD4EDNRAEGFREML4ERBB2ERBB4ESR1ESR2FGFR1FGFR3FLT1FLT3FLT4GAAGABRA1GABRA2GABRA3GABRA4GABRA5GABRA6GABRB1GABRB2GABRB3GABRDGABREGABRG1GABRG2GABRG3GABRPGABRQGHSRGLAGNRHRGPD2GRIN1GRIN2AGRIN2BGRIN2CGRIN2DGRIN3AGRIN3BGSTP1HCN4HCRTR1HCRTR2HDAC1HDAC10HDAC11HDAC2HDAC3HDAC4HDAC5HDAC6HDAC7HDAC8HDAC9HRH1HRH2HRH3HSD11B1HSP90AA1HSP90AB1HTR1AHTR1BHTR1DHTR1EHTR1FHTR2AHTR2BHTR2CHTR3AHTR3BHTR3CHTR3DHTR3EHTR4HTR5AHTR6HTR7IMPDH1IMPDH2ITGA2BITGB3ITKJAK1JAK2KCNA1KCNA10KCNA2KCNA3KCNA4KCNA5KCNA6KCNA7KCNB1KCNB2KCNC1KCNC2KCNC3KCNC4KCND1KCND2KCND3KCNF1KCNG1KCNG2KCNG3KCNG4KCNH1KCNH2KCNH3KCNH4KCNH5KCNH6KCNH7KCNH8KCNJ2KCNJ3KCNJ5KCNK3KCNK9KCNQ1KCNQ2KCNQ3KCNQ4KCNQ5KCNS1KCNS2KCNS3KCNV1KCNV2KDRKITKLKB1LCKMMAOAMAOBMAPK14METMMP1MMP13MMP7MMP8MT-ND1MT-ND2MT-ND3MT-ND4MT-ND4LMT-ND5MT-ND6NDUFA1NDUFA10NDUFA11NDUFA12NDUFA13NDUFA2NDUFA3NDUFA5NDUFA6NDUFA7NDUFA8NDUFA9NDUFAB1NDUFAF1NDUFAF2NDUFAF3NDUFAF4NDUFB1NDUFB10NDUFB11NDUFB2NDUFB3NDUFB4NDUFB5NDUFB6NDUFB7NDUFB8NDUFB9NDUFC1NDUFC2NDUFS1NDUFS2NDUFS3NDUFS4NDUFS5NDUFS6NDUFS7NDUFS8NDUFV1NDUFV2NDUFV3NR3C1NS5ANTRK1NTRK2NTRK3ODC1OPRD1OPRK1OPRM1P2RY12PAHPARP1PDE3APDE3BPDE4APDE4BPDE4CPDE4DPDE5APDE7APDE7BPDE8APDE8BPDGFRAPDGFRBPIK3CAPIK3CDPNPPOLA1POLA2POLD1POLD2POLD3POLD4POLEPOLE2POLE3PPARGPRIM1PRIM2PRKCAPRKCBPRKCDPRKCEPRKCGPRKCHPRKCIPRKCQPRKCZPRKD1PRKD3PTGS1PTGS2RBX1RENRETROCK1ROCK2RPE65RRM1RRM2RRM2BS1PR1S1PR2S1PR3S1PR4S1PR5SCN10ASCN11ASCN1ASCN2ASCN3ASCN4ASCN5ASCN7ASCN8ASCN9ASCNN1ASCNN1BSCNN1GSIGMAR1SLC18A2SLC6A1SLC6A2SLC6A3SLC6A4SLC9A3SRCTACR1TOP1TOP2ATOP2BTTRTYMPdacAdacBdacCembAfolAftsIgyrAgyrBmrcAmrcBmrdAparCparEpolrplArplBrplCrplDrplErplFrplIrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmE2rpmFrpmGrpmG1rpmG2rpmG3rpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO

The experimentally established mechanism targets of Benzo[D]Thiazole. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ MAPK14 known ✓ Q16539 1/20 0.36
▸ SLC6A3 known ✓ Q01959 2/20 0.35
▸ ADRA2A known ✓ P08913 1/20 0.35
▸ DRD2 known ✓ P14416 1/20 0.35
▸ ADRA2B known ✓ P18089 1/20 0.35
▸ ADRA2C known ✓ P18825 1/20 0.35
▸ DRD1 known ✓ P21728 1/20 0.35
▸ OPRM1 known ✓ P35372 1/20 0.35
▸ DRD3 known ✓ P35462 1/20 0.35
▸ OPRK1 known ✓ P41145 1/20 0.35
▸ HTR6 known ✓ P50406 1/20 0.35
▸ SLC6A2 known ✓ P23975 1/20 0.35
▸ SLC6A4 known ✓ P31645 1/20 0.35
▸ ALDH1A1 P00352 3/20 0.95
▸ HSD17B10 Q99714 3/20 0.95
▸ NPC1 O15118 4/20 0.42
▸ RAB9A P51151 4/20 0.42
▸ KDM4E B2RXH2 3/20 0.42
▸ TDP1 Q9NUW8 2/20 0.42
▸ L3MBTL1 Q9Y468 2/20 0.42

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
Benzo[D]Thiazole SCHEMBL27346151 1.00 ALDH1A1 (0.95) ALDH1A1HSD17B10NPC1RAB9AKDM4E
Benzo[D]Thiazole SCHEMBL29466701 0.98 ALDH1A1 (0.91) ALDH1A1HSD17B10NPC1RAB9AKDM4E
Benzo[D]Thiazole SCHEMBL28191275 0.98 ALDH1A1 (0.91) ALDH1A1HSD17B10NPC1RAB9AKDM4E
Benzo[D]Thiazole SCHEMBL10847268 0.97 — —
Benzo[D]Thiazole SCHEMBL31388426 0.97 — —
Benzo[D]Thiazole SCHEMBL451685 0.97 — —
Benzo[D]Thiazole SCHEMBL8430 0.97 — —
Benzo[D]Thiazole SCHEMBL900814 0.97 ALDH1A1 (1.00) ALDH1A1HSD17B10NPC1RAB9AKDM4E
Benzo[D]Thiazole SCHEMBL8501381 0.95 ALDH1A1 (0.86) ALDH1A1HSD17B10NPC1RAB9AKDM4E
Benzo[D]Thiazole SCHEMBL2461444 0.95 ALDH1A1 (0.95) ALDH1A1HSD17B10NPC1RAB9AKDM4E

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-101909628-B As leukotriene A4Aryl substituted bridged or fused diamines as hydrolase modulators JANSSEN PHARMACEUTICA NV 2013-05-29 — — CN claimed
CN-100591679-C Benzimidazole, benzthiazole and benzoxazole derivatives and their use as lta4h modulators JANSSEN PHARMACEUTICA NV 2010-02-24 — — CN claimed
CN-1860117-A Benzimidazole, benzthiazole and benzoxazole derivatives and their use as lta4h modulators JANSSEN PHARMACEUTICA NV (BE) 2006-11-08 — — CN claimed
JP-2157742-A — — None — — JP disclosed
US-12139499-B2 Heteroaryl compounds for treating Huntington's disease PTC THERAPEUTICS, INC. (US) 2024-11-12 — — US disclosed
CN-111933802-B Application of ionic liquid in preparation of perovskite photosensitive layer and perovskite solar cell 昆山协鑫光电材料有限公司 2024-04-19 — — CN disclosed
EP-4284367-A1 FACTOR XIA INHIBITORS Merck Sharp & Dohme LLC (US) 2023-12-06 — — EP disclosed
CN-115315259-A Compounds useful for inhibition of ketohexokinase and methods of making and using the same 因奥必治疗有限公司 2022-11-08 — — CN disclosed
WO-2022164735-A1 FACTOR XIA INHIBITORS MERCK SHARP & DOHME LLC (US) 2022-08-04 — — WO disclosed
US-20210284660-A1 HETEROARYL COMPOUNDS FOR TREATING HUNTINGTON'S DISEASE PTC THERAPEUTICS, INC. 2021-09-16 — — US disclosed
CN-113226356-A Activating pyruvate kinase R 福马治疗股份有限公司 2021-08-06 — — CN disclosed
CN-1216039-A Process for preparing taxol UPJOHN CO (US) 1999-05-05 — — CN disclosed
EP-0772607-A1 WATER-SOLUBLE METHINE COMPOUND AND PHARMACEUTICAL COMPOSITION FOR TREATMENT OF CANCER COMPRISING THE SAME FUJI PHOTO FILM CO., LTD. (JP) 1997-05-14 — — EP disclosed
WO-1996003393-A1 WATER-SOLUBLE METHINE COMPOUND AND PHARMACEUTICAL COMPOSITION FOR TREATMENT OF CANCER COMPRISING THE SAME FUJI PHOTO FILM CO., LTD. (JP) 1996-02-08 — — WO disclosed
US-5314747-A Recording sheets containing cationic sulfur compounds XEROX CORPORATION (US) 1994-05-24 — — US disclosed
US-5013638-A Photographic silver halide element containing small amounts of bromide ions EASTMAN KODAK COMPANY (US) 1991-05-07 — — US disclosed
JP-H02157742-A PHOTOGRAPHIC SILVER HALIDE MATERIAL EASTMAN KODAK CO 1990-06-18 — — JP disclosed
EP-0365220-A2 Photographic silver halide material EASTMAN KODAK COMPANY (a New Jersey corporation) (US) 1990-04-25 — — EP disclosed
US-4128586-A Catalytic reduction of aromatic sulfonyl halides with hydrogen sulfide to yield aromatic thiols ALLIED CHEMICAL CORPORATION (US) 1978-12-05 — — US disclosed
US-4064261-A TRIAZOLOBENOXAZOLE, TRIAZOLOBENZOTHIAZOLE COMPOUNDS ELI LILLY AND COMPANY (US) 1977-12-20 — — 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 (2 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-12139499-B2 Heteroaryl compounds for treating Huntington's disease HTT, HYPK, HDAC6 MAPK14 4079/4885SLC6A3 343/4885ADRA2A 3851/4885
US-20210284660-A1 HETEROARYL COMPOUNDS FOR TREATING HUNTINGTON'S DISEASE HTT, HYPK, HDAC6 MAPK14 4079/4885SLC6A3 343/4885ADRA2A 3851/4885

“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.

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