Phosphoric Acid

Phosphoric Acid

SCHEMBL2536238

O=P([O-])(O)O.O=P([O-])([O-])[O-].[C+4]

nearest known ligand 0.73

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Known targets — ChEMBL curated mechanism

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

The experimentally established mechanism targets of Phosphoric Acid. 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
▸ SLC34A1 Q06495 1/20 0.73
▸ LMNA P02545 3/20 0.40
▸ KDM4E B2RXH2 2/20 0.39
▸ CYP2C19 P33261 1/20 0.39
▸ KMT2A Q03164 1/20 0.39
▸ CA2 P00918 1/20 0.39
▸ TYMS P04818 1/20 0.38
▸ BLM P54132 2/20 0.33
▸ MMP2 P08253 1/20 0.33
▸ THRB P10828 1/20 0.33
▸ MAPK1 P28482 1/20 0.33
▸ HSD17B10 Q99714 1/20 0.33
▸ FDPS P14324 1/20 0.33
▸ TDP1 Q9NUW8 1/20 0.33
▸ CA1 P00915 2/20 0.30
▸ CA4 P22748 2/20 0.30
▸ CA5A P35218 2/20 0.30
▸ CA5B Q9Y2D0 2/20 0.30
▸ CYP3A4 P08684 1/20 0.30
▸ NFKB1 P19838 1/20 0.30

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
Phosphoric Acid SCHEMBL27596260 0.95 SLC34A1 (0.67) SLC34A1LMNAKDM4ECYP2C19KMT2A
Phosphoric Acid SCHEMBL28045127 0.95 SLC34A1 (0.67) SLC34A1LMNAKDM4ECYP2C19KMT2A
Phosphoric Acid SCHEMBL28146677 0.95 SLC34A1 (0.67) SLC34A1LMNAKDM4ECYP2C19KMT2A
Phosphoric Acid SCHEMBL21990207 0.95 — —
Phosphoric Acid SCHEMBL2127340 0.90 SLC34A1 (0.73) SLC34A1LMNAKDM4ECYP2C19KMT2A
Phosphoric Acid SCHEMBL30904476 0.90 SLC34A1 (0.73) SLC34A1LMNAKDM4ECYP2C19KMT2A
Phosphoric Acid SCHEMBL2954685 0.90 SLC34A1 (0.90) SLC34A1LMNAKDM4ECYP2C19KMT2A
Phosphoric Acid SCHEMBL6926626 0.90 SLC34A1 (0.73) SLC34A1LMNAKDM4ECYP2C19KMT2A
Phosphoric Acid SCHEMBL34463363 0.90 SLC34A1 (0.73) SLC34A1LMNAKDM4ECYP2C19KMT2A
Phosphoric Acid SCHEMBL9901846 0.90 SLC34A1 (0.73) SLC34A1LMNAKDM4ECYP2C19KMT2A

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 18 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20220273673-A1 BONE-BINDING COMPOUNDS BRIGHAM YOUNG UNIVERSITY (US) 2022-09-01 — — US disclosed
CN-114585316-A Osseointegrating compounds 布莱阿姆青年大学 2022-06-03 — — CN disclosed
EP-4003201-A1 BONE-BINDING COMPOUNDS Brigham Young University (US) 2022-06-01 — — EP disclosed
WO-2021016583-A1 BONE-BINDING COMPOUNDS BRIGHAM YOUNG UNIVERSITY (US) 2021-01-28 — — WO disclosed
CN-105296024-B A kind of multifunctional diesel oil cetane number improver and preparation method thereof 广昌达新材料技术服务(深圳)股份有限公司 2017-08-29 — — CN disclosed
CN-105296024-A Multifunctional diesel oil cetane number improver and preparation method thereof SHENZHEN CESTO CHEMICAL COMPANY LED 2016-02-03 — — CN disclosed
US-20110256065-A1 Non-Isotopic Detection of Osteoblastic Activity In Vivo Using Modified Bisphosphonates FRANGIONI JOHN V 2011-10-20 — — US disclosed
US-20090123383-A1 Non-Isotopic Detection of Osteoblastic Activity In Vivo Using Modified Bisphosphonates BETH ISRAEL DEACONESS MEDICAL CENTER 2009-05-14 — — US disclosed
US-7374746-B2 Non-isotopic detection of osteoblastic activity in vivo using modified bisphosphonates BETH ISRAEL DEACONEES MEDICAL CENTER (US) 2008-05-20 — — US disclosed
CN-101098960-A X-ray structure of human fpps and use for selecting fpps binding compounds NOVARTIS AG (CH) 2008-01-02 — — CN disclosed
US-20070036724-A1 diagnostic detection of diseases accompanied with an abnormality of calcium hydroxyapatite using in vivo imaging; contrast agent comprising a fluorescent moiety covalently linked to a bisphosphonate moiety such as, alendronate, clodronate, EB-1053, etidronate, ibandronate, incadronate, neridronate FRANGIONI JOHN V 2007-02-15 — — US disclosed
US-20060002857-A1 Non-isotopic detection of osteoplastic activity in vivo using modified bisphosphonates BETH ISRAEL DEACONESS MEDICAL CENTER (US) 2006-01-05 — — US disclosed
US-6869593-B2 Non-isotopic detection of osteoblastic activity in vivo using modified bisphosphonates BETH ISRAEL DEACONESS MEDICAL CENTER (US) 2005-03-22 — — US disclosed
US-20040028611-A1 Non-isotopic detection of osteoblastic activity in vivo using modified bisphosphonates BETH ISRAEL DEACONESS MEDICAL CENTER, OF THE ENTIRE INERST. 2004-02-12 — — US disclosed
EP-1341557-A2 NON-ISOTOPIC DETECTION OF OSTEOBLASTIC ACTIVITY IN VIVO USING MODIFIED BISPHOSPHONATES Beth Israel Deaconess Medical Center (US) 2003-09-10 — — EP disclosed
EP-1131100-B1 THERAPEUTIC COMPOSITIONS FOR METABOLIC BONE DISORDERS OR BONE METASTASES COMPRISING A PHOTOSENSITIZER AND A BISPHOSPHONATE LIGHT SCIENCES CORP (US) 2003-03-12 — — EP disclosed
US-20030018371-A1 Compositions and methods for the treatment of metabolic bone disorders and bone metastases LIGHT SCIENCES CORPORATION 2003-01-23 — — US disclosed
WO-2002038190-A2 NON-ISOTOPIC DETECTION OF OSTEOBLASTIC ACTIVITY IN VIVO USING MODIFIED BISPHOSPHONATES BETH ISRAEL DEACONESS MEDICAL CENTER (US) 2002-05-16 — — 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 (6 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-20040028611-A1 Non-isotopic detection of osteoblastic activity in vivo using modified bisphosphonates SOST, ACP3, PHPT1 SLC34A1 34/4885LMNA 1951/4885KDM4E 3447/4885
US-20110256065-A1 Non-Isotopic Detection of Osteoblastic Activity In Vivo Using Modified Bisphosphonates SOST, ACP3, PHPT1 SLC34A1 34/4885LMNA 1951/4885KDM4E 3447/4885
US-20070036724-A1 diagnostic detection of diseases accompanied with an abnormality of calcium hydroxyapatite using in vivo imaging; contrast agent comprising a fluorescent moiety covalently linked to a bisphosphonate moiety such as, alendronate, clodronate, EB-1053, etidronate, ibandronate, incadronate, neridronate HCAR3, ENTPD3, SLC9A3 SLC34A1 26/4885LMNA 2330/4885KDM4E 4234/4885
US-20060002857-A1 Non-isotopic detection of osteoplastic activity in vivo using modified bisphosphonates SOST, ACP3, ALPP SLC34A1 47/4885LMNA 2226/4885KDM4E 3777/4885
US-20220273673-A1 BONE-BINDING COMPOUNDS CCL5, BMP2, CLTB SLC34A1 35/4885LMNA 1214/4885KDM4E 4206/4885
US-20090123383-A1 Non-Isotopic Detection of Osteoblastic Activity In Vivo Using Modified Bisphosphonates SOST, ACP3, PHPT1 SLC34A1 34/4885LMNA 1951/4885KDM4E 3447/4885

“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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