Known targets — ChEMBL curated mechanism
ABCC9ABL1ACEACHEACVR1ADORA1ADORA2AADORA2BADORA3ADRA1AADRA1BADRA1DADRA2AADRA2BADRA2CADRB1ADRB2ADRB3AGTR1ALOX5ATP4AATP4BBCRBTKCACNA1ACACNA1BCACNA1CCACNA1DCACNA1ECACNA1FCACNA1GCACNA1HCACNA1ICACNA1SCACNA2D1CACNA2D2CACNA2D3CACNA2D4CACNB1CACNB2CACNB3CACNB4CACNG1CACNG2CACNG3CACNG4CACNG5CACNG6CACNG7CACNG8CALCRLCFBCHRM1CHRM2CHRM3CHRM4CHRM5CHRNA1CHRNB1CHRNDCHRNECHRNGCRBNCUL4ACXCR1CXCR2DDB1DDCDHFRDPP4DRD2DRD3DRD4EGFRERBB2ERBB4ESR1ESR2FDPSFKBP1AFLT1FLT3FLT4GARTGHSRGRIA1GRIA2GRIA3GRIA4GRIK1GRIK2GRIK3GRIK4GRIK5GRIN2AGSK3AGSK3BHDAC1HDAC10HDAC11HDAC2HDAC3HDAC4HDAC5HDAC6HDAC7HDAC8HDAC9HRH1HTR1AHTR1BHTR1DHTR1EHTR1FHTR2AHTR2BHTR2CHTR3AHTR3BHTR3CHTR3DHTR3EHTR4HTR5AHTR6HTR7IDH1IDH2IMPA1ITGA2BITGB3JAK1JAK2JAK3KCNJ11KCNK3KCNK9KDRKITMEN1METMMP1MMP13MMP7MMP8NANOD2NS5bODC1OPG057OPRD1OPRK1OPRM1PPARP1PARP2PDE3APDE3BPDE4APDE4BPDE4CPDE4DPDGFRBPIK3CAPIK3CBPIK3CDPIK3CGPIK3R1PIK3R2PIK3R3PIK3R5PKLRPPARDPPATPTGS1PTGS2RBX1ROCK1ROCK2RRM1RRM2RRM2BSCN10ASCN11ASCN1ASCN2ASCN3ASCN4ASCN5ASCN7ASCN8ASCN9ASCNN1ASCNN1BSCNN1GSIGMAR1SLC10A2SLC5A2SLC6A2SLC6A3SLC6A4SLC9A3SYKTACR1THRATHRBTOP1TUBA1ATUBA1BTUBA1CTUBA3CTUBA3ETUBA4ATUBBTUBB1TUBB2ATUBB2BTUBB3TUBB4ATUBB4BTUBB6TUBB8TYK2TYMSVDRampCblablaT-3blaT-4blaT-5blaT-6blaUOE-1dacAdacBdacCfolAfolPftsIgyrAgyrBileSmecAmrcAmrcBmrdAparCparEpbp2pbp4pbpApbpFrplArplBrplCrplDrplErplFrplIrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmE2rpmFrpmGrpmG1rpmG2rpmG3rpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUthyAykgMykgO
The experimentally established mechanism targets of Thiocyanic Acid. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.
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.
| Compound | similarity | top predicted | shared targets | |
|---|---|---|---|---|
| Thiocyanic Acid SCHEMBL29177073 | 1.00 | — | — | |
| Thiocyanic Acid SCHEMBL36431 | 1.00 | — | — | |
| Thiocyanic Acid SCHEMBL4504379 | 0.86 | CA1 (0.30) | — | |
| Thiocyanic Acid SCHEMBL6232486 | 0.86 | CA1 (0.30) | — | |
| Thiocyanic Acid SCHEMBL3862606 | 0.86 | CA1 (0.30) | — | |
| Thiocyanic Acid SCHEMBL11509407 | 0.86 | — | — | |
| Thiocyanic Acid SCHEMBL42005 | 0.86 | CA1 (0.30) | — | |
| Thiocyanic Acid SCHEMBL5146104 | 0.86 | CA1 (0.30) | — | |
| Thiocyanic Acid SCHEMBL4016398 | 0.86 | CA1 (0.30) | — | |
| Thiocyanic Acid SCHEMBL21410334 | 0.86 | — | — |
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.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| US-12415016-B2 | Preparation method for silk fibroin nerve graft fused with NT3 | NANTONG UNIVERSITY (CN) | 2025-09-16 | — | — | US | claimed |
| EP-4011411-B1 | PREPARATION METHOD FOR SILK FIBROIN NERVE GRAFT FUSED WITH NT-3 | UNIV NANTONG (CN) | 2024-09-04 | — | — | EP | claimed |
| US-20230144643-A1 | PREPARATION METHOD FOR SILK FIBROIN NERVE GRAFT FUSED WITH NT3 | NANTONG UNIVERSITY (CN) | 2023-05-11 | — | — | US | claimed |
| US-20230100839-A1 | Liquid Electrolytic Medium and Application in Solid State Li Batteries Thereof | NATIONAL TAIWAN UNIVERSITY OF SCIENCE AND TECHNOLOGY (TW) | 2023-03-30 | — | — | US | claimed |
| EP-4011411-A1 | PREPARATION METHOD FOR SILK FIBROIN NERVE GRAFT FUSED WITH NT3 | Nantong University (CN) | 2022-06-15 | — | — | EP | claimed |
| EP-3818578-A1 | SILYLATED CELLULOSE BASED INTERFACIAL PROTECTIVE LAYER ON A LITHIUM SURFACE | Kemijski Institut (SI) | 2021-05-12 | — | — | EP | claimed |
| US-12506153-B2 | Composition, negative electrode and a battery employing the same | INDUSTRIAL TECHNOLOGY RESEARCH INSTITUTE (TW) | 2025-12-23 | — | — | US | disclosed |
| US-12415016-B2 | Preparation method for silk fibroin nerve graft fused with NT3 | NANTONG UNIVERSITY (CN) | 2025-09-16 | — | — | US | disclosed |
| US-20250210665-A1 | ELECTRODE MATERIAL, ELECTRODE, BATTERY AND METHOD FOR FORMING THE ELECTRODE MATERIAL | INDUSTRIAL TECHNOLOGY RESEARCH INSTITUTE (TW) | 2025-06-26 | — | — | US | disclosed |
| EP-3818578-B1 | SILYLATED CELLULOSE BASED INTERFACIAL PROTECTIVE LAYER ON A LITHIUM SURFACE | KEMIJSKI INST (SI) | 2025-03-12 | — | — | EP | disclosed |
| CN-118908242-A | Method for preparing lithium thiocyanate by using coking desulfurization waste liquid and lithium hydroxide | 江苏燎原环保科技股份有限公司 | 2024-11-08 | — | — | CN | disclosed |
| CN-117954597-B | Polymer coated modified composite positive electrode material and preparation method and application thereof | 高能时代(深圳)新能源科技有限公司 | 2024-09-17 | — | — | CN | disclosed |
| EP-4011411-B1 | PREPARATION METHOD FOR SILK FIBROIN NERVE GRAFT FUSED WITH NT-3 | UNIV NANTONG (CN) | 2024-09-04 | — | — | EP | disclosed |
| EP-0593967-A1 | A process for spinning polypeptide fibers from solutions of lithium thiocyanate and liquefied phenol | E.I. DU PONT DE NEMOURS AND COMPANY (US) | 1994-04-27 | — | — | EP | disclosed |
| US-5252277-A | Process for spinning polypeptide fibers from solutions of lithium thiocyanate and liquefied phenol | E. I. DU PONT DE NEMOURS AND COMPANY (US) | 1993-10-12 | — | — | US | disclosed |
| US-5252285-A | Process for making silk fibroin fibers | E. I. DU PONT DE NEMOURS AND COMPANY (US) | 1993-10-12 | — | — | US | disclosed |
| WO-1993015244-A1 | FIBER-SPINNABLE SOLUTIONS OF SILKWORM FIBROIN | E.I. DU PONT DE NEMOURS AND COMPANY (US) | 1993-08-05 | — | — | WO | disclosed |
| WO-1993004680-A1 | MACROCYCLIC IMMUNOMODULATORS | ABBOTT LABORATORIES (US) | 1993-03-18 | — | — | WO | disclosed |
| US-4743687-A | HYPOTENSIVE AGENTS | HOFFMANN-LA ROCHE INC. (US) | 1988-05-10 | — | — | US | disclosed |
| EP-0211220-A1 | Pyridazo[1,2-a][1,2]diazepine derivatives, intermediate products, process for their preparation and medicaments containing them | F. HOFFMANN-LA ROCHE AG (CH) | 1987-02-25 | — | — | EP | disclosed |