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Poly(Disperse Red 13 acrylate) - Moligand™ , Activator of IP 3R1;Activator of IP 3R2;Activator of IP 3R3, CAS No.142656-03-9, Activator of IP 3R1;Activator of IP 3R2;Activator of IP 3R3

CAS: 142656-03-9 Cat. No.: P486700 Molecular Weight: 420.1
COA
Poly(Disperse Red 13 acrylate) - Moligand™ CAS No(142656-03-9) by Aladdin Scientific
AVAILABLE TO ORDER
GRADE & PURITY Moligand™ ? Moligand™ — Aladdin's line of ligands and bioactive small molecules. Use for receptor, pathway, and binding studies needing defined small-molecule tools.
Synonyms
(1R,2R,3S,4R,5R,6S)-3,5,6-trihydroxycyclohexane-1,2,4-triyl tris[dihydrogen (phosphate)] | 1D-myo-Inositol 1,4,5-trisphosphate | inositol 1,4,5-trisphosphate | Inositol triphosphate (6CI,7CI) | CMC_10501 | d-myo-inositol-1,4,5-triphosphate | 1btn | CMC_72
Storage
Room temperature
★
 ·  off list, applied to all prices below.
Size
Status
Price
Qty
100mg
P486700-100mg
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.

$379.90

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SDS
Safety data
COA
Certificate
DS
Datasheet
SP
Spec sheet
Overview Specifications Names and Identifiers Documentation Advanced Data Taxonomic Classification 3D Structure Associated Targets(Human) Associated Targets(non-human) Mechanisms of Action Certificates（CoA,COO,BSE/TSE and Analysis Chart) Chemical and Physical Properties Solution Calculators Reviews
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Why this grade

Moligand™ Moligand™ for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

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Storage & shipping

Room temperature Ships Check lot-specific COA for exact specifications.

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Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

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Literature proof

Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Overview

Description

NLO polymer

Specifications

Synonyms
(1R, 2R, 3S, 4R, 5R, 6S)-3, 5, 6-trihydroxycyclohexane-1, 2, 4-triyl tris[dihydrogen (phosphate)] | 1D-myo-Inositol 1, 4, 5-trisphosphate | inositol 1, 4, 5-trisphosphate | Inositol triphosphate (6CI, 7CI) | CMC_10501 | d-myo-inositol-1, 4, 5-triphosphate | 1btn | CMC_72
Specifications & Purity
Moligand™
Storage
Room temperature
Grade
Moligand™
Action Type
ACTIVATOR
Mechanism of action
Activator of IP 3R1;Activator of IP 3R2;Activator of IP 3R3
Names and Identifiers
Canonical SmilesC1(C(C(C(C(C1OP(=O)(O)O)O)OP(=O)(O)O)OP(=O)(O)O)O)O
IUPAC Name[(1R,2S,3R,4R,5S,6R)-2,3,5-trihydroxy-4,6-diphosphonooxycyclohexyl] dihydrogen phosphate
InChIKeyMMWCIQZXVOZEGG-XJTPDSDZSA-N
INCHI1S/C6H15O15P3/c7-1-2(8)5(20-23(13,14)15)6(21-24(16,17)18)3(9)4(1)19-22(10,11)12/h1-9H,(H2,10,11,12)(H2,13,14,15)(H2,16,17,18)/t1-,2+,3+,4-,5-,6-/m1/s1
Isomeric SMILES [C@H]1([C@@H]([C@H]([C@@H]([C@H]([C@@H]1OP(=O)(O)O)O)OP(=O)(O)O)OP(=O)(O)O)O)O
Alternate CAS 85166-31-0
MeSH Entry Terms 1,4,5-InsP3;1,4,5-IP3;Inositol 1,4,5-Triphosphate;Inositol 1,4,5-Trisphosphate;Myo-Inositol 1,4,5-Trisphosphate;Myoinositol 1,4,5-Triphosphate
Molecular Weight 420.1
Reaxy-Rn 8514194
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=8514194&ln=

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

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✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

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📊 Datasheet

Quick-reference summary of product specifications and applications.

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🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

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Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganic oxygen compounds
ClassOrganooxygen compounds
SubclassAlcohols and polyols
Intermediate Tree Nodes Cyclic alcohols and derivatives - Cyclitols and derivatives
Direct ParentInositol phosphates
Alternative Parents Monoalkyl phosphates  Cyclohexanols  Polyols  Organic oxides  Hydrocarbon derivatives  
Molecular FrameworkAliphatic homomonocyclic compounds
Substituents Inositol phosphate - Monoalkyl phosphate - Cyclohexanol - Alkyl phosphate - Phosphoric acid ester - Organic phosphoric acid derivative - Secondary alcohol - Polyol - Organic oxide - Hydrocarbon derivative - Aliphatic homomonocyclic compound
DescriptionThis compound belongs to the class of organic compounds known as inositol phosphates. These are compounds containing a phosphate group attached to an inositol (or cyclohexanehexol) moiety.
External Descriptors myo-inositol trisphosphate
3D Structure
Interactive Chemical Structure Model





Associated Targets(Human)
ITPR1 Tchem Inositol 1,4,5-trisphosphate receptor type 1 (2 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
ITPR2 Tbio Inositol 1,4,5-trisphosphate receptor type 2 (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
ITPR3 Tchem Inositol 1,4,5-trisphosphate receptor type 3 (1 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
INPP5A Tchem Type I inositol-1,4,5-trisphosphate 5-phosphatase (17 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ITPR1 Tchem Inositol 1,4,5-trisphosphate receptor type 1 (23 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Homo sapiens (32628 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SH-SY5Y (11521 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Associated Targets(non-human)
Itpr3 Inositol 1,4,5-trisphosphate receptor type 3 (14 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Plcl1 Inositol 1,4,5-trisphosphate binding protein (3 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Itpka Inositol-trisphosphate 3-kinase A (9 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Type 1 InsP3 receptor isoform S2 (25 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Bos taurus (956 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Oryctolagus cuniculus (11301 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Rattus norvegicus (775804 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
L1210 (27553 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
RBL-1 (51 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mechanisms of Action
Certificates（CoA,COO,BSE/TSE and Analysis Chart)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:
Chemical and Physical Properties
Solubility chloroform: soluble; toluene: soluble
Flash Point(°F)Not applicable
Flash Point(°C)Not applicable
Melt Point(°C)Tg74℃ (onset)
Molecular Weight420.100 g/mol
XLogP3-7.000
Hydrogen Bond Donor Count9
Hydrogen Bond Acceptor Count15
Rotatable Bond Count6
Exact Mass419.962 Da
Monoisotopic Mass419.962 Da
Topological Polar Surface Area261.000 Ų
Heavy Atom Count24
Formal Charge0
Complexity574.000
Isotope Atom Count0
Defined Atom Stereocenter Count6
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Solution Calculators
Reviews

Customer Reviews

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View related series

IP3R1 Activator (3) IP3R2 Activator (2) IP3R3 Activator (1)
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