Tetrabuthylammonium

Tetrabuthylammonium

SCHEMBL909400

CC(C)(C)OP(=O)([O-])OC(C)(C)C.CCCC[N+](CCCC)(CCCC)CCCC

nearest known ligand 0.46

Full drug profile on Sugi Atlas →

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
SLC22A1 O15245 3/20 0.46
LMNA P02545 1/20 0.42
ESR1 P03372 1/20 0.42
ADORA3 P0DMS8 1/20 0.42
CDC25A P30304 1/20 0.42
AGTR1 P30556 1/20 0.42
AKT1 P31749 1/20 0.42
ADRA1A P35348 1/20 0.42
KCNH2 Q12809 1/20 0.42
SLC22A2 O15244 1/20 0.41
ALDH1A1 P00352 1/20 0.38
TP53 P04637 1/20 0.38
CYP3A4 P08684 1/20 0.38
ALOX15 P16050 1/20 0.38
TSHR P16473 1/20 0.38
ALOX12 P18054 1/20 0.38
SMN1; SMN2 Q16637 1/20 0.38
HIF1A Q16665 1/20 0.38
HSD17B10 Q99714 1/20 0.38
DNM1 Q05193 4/20 0.35

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
Tetrabuthylammonium SCHEMBL28999740 1.00 SLC22A1 (0.46) SLC22A1LMNAESR1ADORA3CDC25A
Tetrabuthylammonium SCHEMBL25270463 0.89 SLC22A1 (0.46) SLC22A1LMNAESR1ADORA3CDC25A
Tetrabuthylammonium SCHEMBL49814 0.81 SLC22A1 (0.71) SLC22A1LMNAESR1ADORA3CDC25A
Tetrabuthylammonium SCHEMBL19834900 0.81 SLC22A1 (0.71) SLC22A1LMNAESR1ADORA3CDC25A
Tetrabuthylammonium SCHEMBL6283913 0.81 SLC22A1 (0.46) SLC22A1SLC22A2ALDH1A1TP53CYP3A4
Tetrabuthylammonium SCHEMBL25270462 0.81 SMPD1 (0.50) SLC22A1SLC22A2ALDH1A1TP53CYP3A4
Tetrabuthylammonium SCHEMBL703752 0.79 SLC22A1 (0.67) SLC22A1LMNAESR1ADORA3CDC25A
Tetrabuthylammonium SCHEMBL31067882 0.79 SLC22A1 (0.67) SLC22A1LMNAESR1ADORA3CDC25A
Tetrabuthylammonium SCHEMBL3141779 0.79 SLC22A1 (0.67) SLC22A1LMNAESR1ADORA3CDC25A
Tetrabuthylammonium SCHEMBL28547695 0.79 SLC22A1 (0.67) SLC22A1LMNAESR1ADORA3CDC25A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-122055373-A Bridged tricyclic carbamoyl pyridone compounds and uses thereof 吉利德科学公司 2026-05-15 CN disclosed
EP-4719608-A1 QUINAZOLINYL-INDAZOLE DERIVATIVES AS THERAPEUTIC COMPOUNDS FOR HIV GILEAD SCIENCES, INC. (US) 2026-04-08 EP disclosed
US-20260035357-A1 THERAPEUTIC COMPOUNDS FOR HIV VIRUS INFECTION GILEAD SCIENCE INC (US) 2026-02-05 US disclosed
US-12404262-B2 Therapeutic compounds for HIV virus infection GILEAD SCIENCES, INC. (US) 2025-09-02 US disclosed
EP-4594319-A1 BICYCLIC COMPOUNDS Aligos Therapeutics, Inc. (US) 2025-08-06 EP disclosed
US-20250230296-A1 POLYVINYLIDENE FLUORIDE RESIN COMPOSITION AND MOLDED BODY KUREHA CORPORATION (JP) 2025-07-17 US disclosed
EP-4566608-A2 THERAPEUTIC COMPOUNDS FOR HIV VIRUS INFECTION Gilead Sciences, Inc. (US) 2025-06-11 EP disclosed
US-20250179102-A1 THERAPEUTICS COMPOUNDS FOR HIV VIRUS INFECTION GILEAD SCIENCES, INC. 2025-06-05 US disclosed
EP-4440702-B1 THERAPEUTIC COMPOUNDS FOR HIV VIRUS INFECTION GILEAD SCIENCES INC (US) 2025-05-21 EP disclosed
EP-4445900-B1 THERAPEUTIC COMPOUNDS FOR HIV VIRUS INFECTION GILEAD SCIENCES INC (US) 2025-05-21 EP disclosed
WO-2001052852-A1 WATER SOLUBLE PRODRUGS OF AZOLE COMPOUNDS BRISTOL-MYERS SQUIBB COMPANY (US) 2001-07-26 WO disclosed
US-5959028-A UNSATURATED CARBONYL COMPOUND AND ACTIVE METHYLENE GROUP COMPOUND, ASYMMETRIC MALONATE ESTER FOR PROTECTIVE COATINGS NIPPON PAINT CO., LTD. (JP) 1999-09-28 US disclosed
EP-0651023-B1 Curable resin composition for coating uses NIPPON PAINT CO LTD (JP) 1999-07-14 EP disclosed
EP-0737725-B1 Curable resin composition for coating use NIPPON PAINT CO LTD (JP) 1998-07-01 EP disclosed
US-5739230-A CURABLE THROUGH A MICHAEL REACTION BETWEEN A COMPONENT HAVING A PLURALITY OF ALPHA,BETA-UNSATURATED CARBONYL GROUPS AND A COMPONENT HAVING A PLURALITY OF ACTIVATED METHYLENE GROUPS NIPPON PAINT CO., LTD. (JP) 1998-04-14 US disclosed
EP-0808860-A2 Curable resin composition for coating use NIPPON PAINT CO., LTD. (JP) 1997-11-26 EP disclosed
EP-0737725-A1 Curable resin composition for coating use Nippon Paint Co., Ltd. (JP) 1996-10-16 EP disclosed
US-5565525-A CURABLE THROUGH MICHAEL REACTION NIPPON PAINT CO., LTD. (JP) 1996-10-15 US disclosed
EP-0651023-A2 Curable resin composition for coating uses Nippon Paint Co., Ltd. (JP) 1995-05-03 EP disclosed
US-4678609-A Process for the preparation of corticosteroid-21-phosphoric acids and their salts and the corticosteroid-21-phosphoric acid triesters HOECHST AKTIENGESELLSCHAFT (DE) 1987-07-07 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 (3 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-20250179102-A1 THERAPEUTICS COMPOUNDS FOR HIV VIRUS INFECTION CD4, HAVCR2, MAVS SLC22A1 2867/4885LMNA 3425/4885ESR1 2616/4885
US-12404262-B2 Therapeutic compounds for HIV virus infection HAVCR2, MAVS, CD4 SLC22A1 3351/4885LMNA 3518/4885ESR1 2647/4885
US-20260035357-A1 THERAPEUTIC COMPOUNDS FOR HIV VIRUS INFECTION CCR10, CCR1, CCR3 SLC22A1 2056/4885LMNA 3767/4885ESR1 1434/4885

“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.